| ID: 130067142 | ATAC-STARR-seq lymphoblastoid active region 18790 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25880625..25880804) | | |
| ID: 130067141 | ATAC-STARR-seq lymphoblastoid active region 18789 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25750110..25750159) | | |
| ID: 130067140 | ATAC-STARR-seq lymphoblastoid active region 18788 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25702918..25703017) | | |
| ID: 127895665 | NANOG-H3K27ac hESC enhancer GRCh37_chr22:26462849-26463654 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (26066883..26067688) | | |
| ID: 127895664 | NANOG-H3K27ac hESC enhancer GRCh37_chr22:26462043-26462848 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (26066077..26066882) | | |
| ID: 127895663 | H3K4me1 hESC enhancer GRCh37_chr22:26388463-26388963 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25992497..25992997) | | |
| ID: 127895662 | H3K27ac hESC enhancer GRCh37_chr22:26366955-26367745 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25970989..25971779) | | |
| ID: 127895661 | H3K27ac hESC enhancer GRCh37_chr22:26366162-26366954 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25970196..25970988) | | |
| ID: 127895660 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:26339189-26339725 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25943222..25943758) | | |
| ID: 127895659 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:26338651-26339188 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25942684..25943221) | | |
| ID: 127895658 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:26331174-26331797 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25935207..25935830) | | |
| ID: 127895657 | H3K4me1 hESC enhancer GRCh37_chr22:26242211-26242711 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25846244..25846744) | | |
| ID: 127895656 | H3K4me1 hESC enhancer GRCh37_chr22:26173587-26174087 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25777620..25778120) | | |
| ID: 127895655 | H3K4me1 hESC enhancer GRCh37_chr22:26173086-26173586 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25777119..25777619) | | |
| ID: 127895654 | H3K4me1 hESC enhancer GRCh37_chr22:26150817-26151326 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25754850..25755359) | | |
| ID: 127895653 | H3K4me1 hESC enhancer GRCh37_chr22:26150305-26150816 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25754338..25754849) | | |
| ID: 126863103 | BRD4-independent group 4 enhancer GRCh37_chr22:26099534-26100733 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25703567..25704766) | | |
| ID: 121853038 | Sharpr-MPRA regulatory region 2919 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25759882..25760176) | | |
| ID: 121853037 | Sharpr-MPRA regulatory region 14204 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25747462..25747756) | | |
| ID: 106480886 | RN7SK pseudogene 169 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25963983..25964273, complement) | | |