| ID: 127828698 | H3K4me1 hESC enhancer GRCh37_chr14:102530418-102531305 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (102064081..102064968) | | |
| ID: 127828697 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:102523379-102524082 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (102057042..102057745) | | |
| ID: 127828696 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:102522673-102523378 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (102056336..102057041) | | |
| ID: 127828695 | H3K4me1 hESC enhancer GRCh37_chr14:102515797-102516781 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (102049460..102050444) | | |
| ID: 127828694 | NANOG hESC enhancer GRCh37_chr14:102474230-102474777 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (102007893..102008440) | | |
| ID: 127828693 | H3K4me1 hESC enhancer GRCh37_chr14:102436952-102437452 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (101970615..101971115) | | |
| ID: 127828692 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:102431258-102431867 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (101964921..101965530) | | |
| ID: 127828691 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:102430647-102431257 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (101964310..101964920) | | |
| ID: 127828690 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:102413937-102414598 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (101947600..101948261) | | |
| ID: 127828689 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr14:102411955-102412614 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (101945618..101946277) | | |
| ID: 126862060 | BRD4-independent group 4 enhancer GRCh37_chr14:102493659-102494858 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (102027322..102028521) | | |
| ID: 125078040 | Sharpr-MPRA regulatory region 9666 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (102050632..102050926) | | |
| ID: 107984661 | uncharacterized LOC107984661 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (102036315..102039037, complement) | | |
| ID: 1778 | dynein cytoplasmic 1 heavy chain 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (101964573..102056443) | CDCBM13, CMT2O, DHC1, DHC1a, DNCH1, DNCL, DNECL, DYHC, Dnchc1, HL-3, SMALED1, p22 | 600112 |