| ID: 127267414 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:10695017-10695979 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10634960..10635922) | | |
| ID: 127267413 | H3K4me1 hESC enhancer GRCh37_chr1:10693091-10694054 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10633034..10633997) | | |
| ID: 127267412 | H3K4me1 hESC enhancer GRCh37_chr1:10682167-10682666 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10622110..10622609) | | |
| ID: 127267411 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:10678456-10679010 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10618399..10618953) | | |
| ID: 127267410 | H3K4me1 hESC enhancer GRCh37_chr1:10676275-10676958 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10616218..10616901) | | |
| ID: 127267409 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:10675589-10676274 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10615532..10616217) | | |
| ID: 127267408 | H3K4me1 hESC enhancer GRCh37_chr1:10663073-10663572 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10603016..10603515) | | |
| ID: 127267407 | H3K4me1 hESC enhancer GRCh37_chr1:10662571-10663072 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10602514..10603015) | | |
| ID: 127267406 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:10654659-10655176 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10594602..10595119) | | |
| ID: 127267405 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:10654141-10654658 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10594084..10594601) | | |
| ID: 127267404 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:10616013-10616674 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10555956..10556617) | | |
| ID: 127267403 | H3K4me1 hESC enhancer GRCh37_chr1:10601005-10601548 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10540948..10541491) | | |
| ID: 127267402 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:10568725-10569413 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10508668..10509356) | | |
| ID: 127267401 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:10534116-10535081 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10474059..10475036) | | |
| ID: 126805616 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:10683990-10685189 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10623933..10625132) | | |
| ID: 126805615 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:10588102-10589301 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10528045..10529244) | | |
| ID: 121967075 | Sharpr-MPRA regulatory region 3136 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10591012..10591306) | | |
| ID: 121967074 | Sharpr-MPRA regulatory region 5895 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10494672..10494966) | | |
| ID: 106481089 | RNA, 7SL, cytoplasmic 614, pseudogene [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10616836..10617115) | | |
| ID: 100526739 | CENPS-CORT readthrough [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10430433..10452153) | APITD1, APITD1-CORT, CENP-S, CENPS, FAAP16, MHF1 | |