| ID: 127822453 | NANOG hESC enhancer GRCh37_chr11:103454489-103455412 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103583761..103584684) | | |
| ID: 127822452 | NANOG hESC enhancer GRCh37_chr11:103452251-103453176 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103581523..103582448) | | |
| ID: 127822451 | H3K4me1 hESC enhancer GRCh37_chr11:103012329-103012830 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103141600..103142101) | | |
| ID: 127822450 | H3K27ac hESC enhancer GRCh37_chr11:102962627-102963244 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103091898..103092515) | | |
| ID: 124625829 | H3K27ac hESC enhancer GRCh37_chr11:102962009-102962626 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103091280..103091897) | | |
| ID: 107075273 | MT-ATP6 pseudogene 15 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103402588..103403422, complement) | | |
| ID: 107075265 | MT-CO1 pseudogene 15 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103404309..103405834, complement) | | |
| ID: 107075154 | MT-CO3 pseudogene 15 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103402013..103402586, complement) | | |
| ID: 107075147 | MT-CO2 pseudogene 15 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103403512..103404167, complement) | | |
| ID: 100873349 | MT-ND2 pseudogene 26 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103406219..103407241, complement) | | |
| ID: 100506721 | MT-ND1 pseudogene 36 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103407441..103408376, complement) | | |
| ID: 84259 | defective in cullin neddylation 1 domain containing 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103050686..103092160, complement) | DCNL5, SCCRO5 | 616522 |
| ID: 79659 | dynein cytoplasmic 2 heavy chain 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103109426..103479863) | ATD3, DHC1b, DHC2, DNCH2, DYH1B, SRPS2B, SRTD3, hdhc11 | 603297 |