| ID: 127827099 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:114236917-114237890 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113582602..113583575) | | |
| ID: 127827098 | H3K4me1 hESC enhancer GRCh37_chr13:114206049-114206550 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113551734..113552235) | | |
| ID: 127827097 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:114200259-114201002 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113545944..113546687) | | |
| ID: 127827096 | H3K4me1 hESC enhancer GRCh37_chr13:114110333-114111263 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113456018..113456948) | | |
| ID: 126861870 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr13:114195260-114196459 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113540945..113542144) | | |
| ID: 100873860 | RNA, U1 small nuclear 16, pseudogene [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113478915..113479071, complement) | U1.64 | |
| ID: 55208 | defective in cullin neddylation 1 domain containing 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113455819..113491563, complement) | C13orf17, DCNL2 | |
| ID: 55002 | transmembrane and coiled-coil domains 3 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113491021..113550229) | C13orf11 | 617134 |