| ID: 127882503 | H3K4me1 hESC enhancer GRCh37_chr1:151495500-151496035 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151523024..151523559) | | |
| ID: 127270327 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:151512562-151513077 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151540086..151540601) | | |
| ID: 127270326 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:151511530-151512046 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151539054..151539570) | | |
| ID: 127270325 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:151485823-151486398 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151513347..151513922) | | |
| ID: 127270324 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:151485246-151485822 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151512770..151513346) | | |
| ID: 127270323 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:151483517-151484092 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151511038..151511616) | | |
| ID: 127270322 | H3K27ac hESC enhancer GRCh37_chr1:151482940-151483516 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151510464..151511040) | | |
| ID: 127270321 | H3K4me1 hESC enhancer GRCh37_chr1:151476367-151476867 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151503891..151504391) | | |
| ID: 126805859 | BRD4-independent group 4 enhancer GRCh37_chr1:151495990-151497189 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151523514..151524713) | | |
| ID: 124900437 | small nucleolar RNA SNORA44 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151527831..151527938, complement) | | |
| ID: 121725055 | Sharpr-MPRA regulatory region 7521 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151443933..151444227) | | |
| ID: 57530 | cingulin [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151510170..151538692) | | 609473 |
| ID: 23126 | pogo transposable element derived with ZNF domain [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151402724..151459494, complement) | MRD37, WHSUS, ZNF280E, ZNF635, ZNF635m | 614787 |
| ID: 7286 | tuftelin 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151540309..151583583) | WHSF | 600087 |