ID: 127894962 | H3K4me1 hESC enhancer GRCh37_chr21:46045935-46046630 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44626018..44626713) | | |
ID: 127894961 | H3K4me1 hESC enhancer GRCh37_chr21:46036915-46037661 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44616998..44617744) | | |
ID: 127894960 | H3K4me1 hESC enhancer GRCh37_chr21:46032635-46033283 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44612718..44613366) | | |
ID: 127894959 | H3K4me1 hESC enhancer GRCh37_chr21:46031985-46032634 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44612068..44612717) | | |
ID: 127894958 | H3K4me1 hESC enhancer GRCh37_chr21:46022863-46023717 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44602946..44603800) | | |
ID: 127894957 | H3K4me1 hESC enhancer GRCh37_chr21:46022006-46022862 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44602089..44602945) | | |
ID: 127894956 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46021146-46021905 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44601231..44601990) | | |
ID: 127894955 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46020385-46021145 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44600481..44601230) | | |
ID: 386681 | keratin associated protein 10-8 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44612079..44612954) | KAP10.8, KRTAP18-8, KRTAP18.8 | |
ID: 386676 | keratin associated protein 10-9 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44627093..44628378) | KAP10.9, KAP18.9, KRTAP18-9 | |
ID: 386675 | keratin associated protein 10-7 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44600597..44602174) | KAP10.7, KAP18.7, KRTAP18-7 | |
ID: 386674 | keratin associated protein 10-6 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44591268..44592505, complement) | KAP10.6, KAP18.6, KRTAP18-6, KRTAP18.6 | |
ID: 353333 | keratin associated protein 10-10 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44637356..44638455) | KAP10.10, KAP18.10, KRTAP18-10, KRTAP18.10 | |
ID: 54084 | thrombospondin type laminin G domain and EAR repeats [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44497893..44711572, complement) | C21orf29, DFNB98, ECTD14, STHAG10, TSP-EAR | 612920 |