ID: 127822208 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr11:77464243-77464827 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (77753198..77753782) | | |
ID: 127822207 | H3K27ac hESC enhancer GRCh37_chr11:77348567-77349086 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (77637522..77638041) | | |
ID: 116216158 | CRISPRi-validated cis-regulatory element chr11.4537 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (77644627..77644860) | | |
ID: 107984369 | uncharacterized LOC107984369 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (77639808..77646258) | | |
ID: 100874308 | RSF1 intronic transcript 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (77738169..77739709, complement) | | |
ID: 51773 | remodeling and spacing factor 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (77660009..77872232, complement) | HBXAP, RSF-1, XAP8, p325 | 608522 |
ID: 2508 | ferritin heavy chain 1 pseudogene 16 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (77734315..77735232, complement) | FTH2, FTHL16 | |
ID: 1207 | chloride nucleotide-sensitive channel 1A [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (77614530..77637794, complement) | CLCI, CLNS1B, ICln | 602158 |