Data table |
ID |
COL |
ROW |
SPOT_ID |
CONTROL_TYPE |
GB_ACC |
GENE_SYMBOL |
GENE_NAME |
ACCESSION_STRING |
CHROMOSOMAL_LOCATION |
CYTOBAND |
DESCRIPTION |
GB_RANGE |
1 |
103 |
430 |
HsCGHBrightCorner |
pos |
|
|
|
|
|
|
|
|
2 |
103 |
428 |
NegativeControl |
neg |
|
|
|
|
|
|
|
|
3 |
103 |
426 |
A_17_P02000824 |
FALSE |
NM_173351 |
OR6B3 |
|
ref|NM_173351|ref|OR6B3:-2653|ens|ENST00000328627:442304|ens|ENST00000355104:-5743|ens|ENST00000319423:-2644 |
chr2:240708110-240708155 |
|
PROMOTER |
NC_000002.9[240708110..240708155] |
4 |
103 |
424 |
A_17_P01063480 |
FALSE |
NM_003353 |
UCN |
|
ref|NM_003353|ref|UCN:-442|ref|NM_187841:25973|ref|NM_002437:13859|ens|ENST00000296099:-442 |
chr2:027443201-027443246 |
|
PROMOTER |
NC_000002.9[027443201..027443246] |
5 |
103 |
422 |
A_17_P01846782 |
FALSE |
NM_005896 |
IDH1 |
|
ref|NM_005896|ref|IDH1:16|ccds|CCDS2381.1:-3515|mgcs|BC012846:-880 |
chr2:208945274-208945319 |
|
INSIDE |
NC_000002.9[208945274..208945319] |
6 |
103 |
420 |
A_17_P00960753 |
FALSE |
NM_003108 |
SOX11 |
|
ref|NM_003108|ref|SOX11:-6787|ens|ENST00000322002:-6787 |
chr2:005776586-005776632 |
|
PROMOTER |
NC_000002.9[005776586..005776632] |
7 |
103 |
418 |
A_17_P01806059 |
FALSE |
NM_153031 |
FLJ32063 |
|
ref|NM_153031|ref|FLJ32063:996|ens|ENST00000295075:996 |
chr2:200161098-200161143 |
|
INSIDE |
NC_000002.9[200161098..200161143] |
8 |
103 |
416 |
LACC:GD24C_4_1 |
pos |
|
|
|
|
|
|
|
|
9 |
103 |
414 |
A_17_P02237210 |
FALSE |
NM_033010 |
PCBP4 |
|
ref|NM_033010|ref|PCBP4:-4311|ref|NM_080865:11823|ref|NM_033009:-5567|ref|NM_033008:250|ens|ENST00000337024:-4311 |
chr3:051976237-051976282 |
|
PROMOTER |
NC_000003.9[051976237..051976282] |
10 |
103 |
412 |
A_17_P02188560 |
FALSE |
NM_001248 |
ENTPD3 |
|
ref|NM_001248|ref|ENTPD3:-422|mgcs|BC029869:-1266 |
chr3:040403247-040403302 |
|
PROMOTER |
NC_000003.9[040403247..040403302] |
11 |
103 |
410 |
A_17_P01256902 |
FALSE |
NM_014882 |
ARHGAP25 |
|
ref|NM_014882|ref|ARHGAP25:2099|ref|NM_001007231:42064|mgcs|BC039591:1960 |
chr2:068915655-068915709 |
|
INSIDE |
NC_000002.9[068915655..068915709] |
12 |
103 |
408 |
A_17_P01186820 |
FALSE |
NM_006794 |
GPR75 |
|
ref|NM_006794|ref|GPR75:5366|mgcs|BC067476:223 |
chr2:053993329-053993378 |
|
INSIDE |
NC_000002.9[053993329..053993378] |
13 |
103 |
406 |
A_17_P00986509 |
FALSE |
NM_144583 |
ATP6V1C2 |
|
ref|NM_144583|ref|ATP6V1C2:840|mgcs|BC012142:-293 |
chr2:010813236-010813284 |
|
INSIDE |
NC_000002.9[010813236..010813284] |
14 |
103 |
404 |
A_17_P01111509 |
FALSE |
NM_144713 |
FAM82A |
|
ref|NM_144713|ref|FAM82A:-1453|ens|ENST00000234195:-1453|ens|ENST00000357809:23663|mgcs|BC024243:20251 |
chr2:038087773-038087833 |
|
PROMOTER |
NC_000002.9[038087773..038087833] |
15 |
103 |
402 |
A_17_P02062527 |
FALSE |
NM_003178 |
SYN2 |
|
ref|NM_003178|ref|SYN2:-7280|ref|NM_133625:-7280 |
chr3:012013554-012013614 |
|
PROMOTER |
NC_000003.9[012013554..012013614] |
16 |
103 |
400 |
A_17_P02244716 |
FALSE |
NM_000720 |
CACNA1D |
|
ref|NM_000720|ref|CACNA1D:-1054|ens|ENST00000350061:-1172 |
chr3:053503039-053503084 |
|
PROMOTER |
NC_000003.9[053503039..053503084] |
17 |
103 |
398 |
A_17_P01756160 |
FALSE |
NM_000090 |
COL3A1 |
|
ref|NM_000090|ref|COL3A1:1819|mgcs|BC028178:1806 |
chr2:189666393-189666453 |
|
INSIDE |
NC_000002.9[189666393..189666453] |
18 |
103 |
396 |
A_17_P02268254 |
FALSE |
NM_007042 |
RPP14 |
|
ref|NM_007042|ref|RPP14:-3946|ref|NM_020676:64747|ccds|CCDS2888.1:-8001|ccds|CCDS2887.1:45742|mgcs|BC002441:-3977 |
chr3:058263065-058263125 |
|
PROMOTER |
NC_000003.9[058263065..058263125] |
19 |
103 |
394 |
A_17_P00933000 |
FALSE |
NM_030645 |
SH3BP5L-ZNF672 |
|
ref|NM_030645|ref|NM_024836|ref|SH3BP5L:-7826|ref|ZNF672:-4549|mgcs|BC008872:-4741|mgcs|BC017254:-8805|ens|ENST00000343022:-7148 |
chr1:245337701-245337761 |
|
DIVERGENT_PROMOTER |
NC_000001.8[245337701..245337761] |
20 |
103 |
392 |
A_17_P01963367 |
FALSE |
NM_000751 |
CHRND |
|
ref|NM_000751|ref|CHRND:7182|mgcs|BC093923:7210 |
chr2:233223578-233223638 |
|
INSIDE |
NC_000002.9[233223578..233223638] |