ID: 127888262 | H3K4me1 hESC enhancer GRCh37_chr17:76914785-76915760 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78918703..78919678) | | |
ID: 127888261 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:76912639-76913334 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78916557..78917252) | | |
ID: 127888260 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:76911943-76912638 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78915861..78916556) | | |
ID: 127888259 | H3K4me1 hESC enhancer GRCh37_chr17:76898462-76899062 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78902380..78902980) | | |
ID: 127888258 | H3K4me1 hESC enhancer GRCh37_chr17:76877535-76878035 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78881453..78881953) | | |
ID: 127888257 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:76875849-76876740 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78879767..78880658) | | |
ID: 127888256 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:76874955-76875848 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78878873..78879766) | | |
ID: 127888255 | H3K4me1 hESC enhancer GRCh37_chr17:76869765-76870265 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78873683..78874183) | | |
ID: 127888254 | H3K4me1 hESC enhancer GRCh37_chr17:76834865-76835379 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78838783..78839297) | | |
ID: 125316808 | Sharpr-MPRA regulatory region 14803 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78939707..78940001) | | |
ID: 124904068 | uncharacterized LOC124904068 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78862225..78868230) | | |
ID: 124904067 | uncharacterized LOC124904067 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78841114..78846792) | | |
ID: 121852953 | Sharpr-MPRA regulatory region 6708 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78975087..78975381) | | |
ID: 121627815 | Sharpr-MPRA regulatory region 5911/8204 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78883807..78884101) | | |
ID: 112533675 | Sharpr-MPRA regulatory region 3779 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78862307..78862601) | | |
ID: 100653515 | CEP295 N-terminal like [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78890579..78903201, complement) | DDC8, KIAA1731NL | |
ID: 100129357 | ribosomal protein L9 pseudogene 29 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78845847..78846437, complement) | RPL9_17_1576 | |
ID: 57602 | ubiquitin specific peptidase 36 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78787381..78841439, complement) | DUB1 | 612543 |
ID: 7077 | TIMP metallopeptidase inhibitor 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78852977..78925387, complement) | CSC-21K, DDC8 | 188825 |
ID: 3959 | galectin 3 binding protein [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78971255..78979923, complement) | 90K, BTBD17B, CyCAP, M2BP, MAC-2-BP, TANGO10B, gp90 | 600626 |