| ID: 127821560 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr11:66340443-66341194 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66572972..66573723) | | |
| ID: 127821559 | H3K4me1 hESC enhancer GRCh37_chr11:66332233-66332732 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66564762..66565261) | | |
| ID: 127821558 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:66307071-66307841 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66539600..66540370) | | |
| ID: 127821557 | H3K4me1 hESC enhancer GRCh37_chr11:66298847-66299424 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66531376..66531953) | | |
| ID: 124500676 | Sharpr-MPRA regulatory region 510 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66570098..66570392) | | |
| ID: 124500675 | Sharpr-MPRA regulatory region 1034 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66549218..66549512) | | |
| ID: 254359 | zinc finger DHHC-type containing 24 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66520625..66546048, complement) | | |
| ID: 8722 | cathepsin F [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66563464..66568606, complement) | CATSF, CLN13 | 603539 |
| ID: 582 | Bardet-Biedl syndrome 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66510635..66533598) | BBS2L2 | 209901 |
| ID: 89 | actinin alpha 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66546395..66563334) | ACTN3D | 102574 |