ID: 127820284 | NANOG hESC enhancer GRCh37_chr11:5642663-5643271 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (5621433..5622041) | | |
ID: 127820283 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:5617638-5618555 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (5596408..5597325) | | |
ID: 126861119 | BRD4-independent group 4 enhancer GRCh37_chr11:5700031-5701230 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (5678801..5680000) | | |
ID: 121832784 | Sharpr-MPRA regulatory region 11830 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (5595959..5596253) | | |
ID: 121392889 | Sharpr-MPRA regulatory region 4679 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (5600359..5600653) | | |
ID: 107984302 | uncharacterized LOC107984302 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (5655495..5660832, complement) | | |
ID: 445372 | TRIM6-TRIM34 readthrough [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (5596637..5644398) | IFP1, RNF21, RNF89, TRIM34, TRIM6 | |
ID: 117854 | tripartite motif containing 6 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (5596111..5612952) | RNF89 | 607564 |
ID: 85363 | tripartite motif containing 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (5588635..5685074, complement) | RNF88alpha, TRIM5 | 608487 |
ID: 53840 | tripartite motif containing 34 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (5619944..5644398) | IFP1, RNF21 | 605684 |