| ID: 129934275 | ATAC-STARR-seq lymphoblastoid active region 16169 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88615899..88616108) | | |
| ID: 129934274 | ATAC-STARR-seq lymphoblastoid active region 16168 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88614631..88614690) | | |
| ID: 127273974 | NANOG-H3K27ac hESC enhancer GRCh37_chr2:88927437-88928116 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88627919..88628598) | | |
| ID: 127273973 | NANOG-H3K27ac hESC enhancer GRCh37_chr2:88926757-88927436 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88627239..88627918) | | |
| ID: 127273972 | H3K27ac hESC enhancer GRCh37_chr2:88926077-88926756 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88626559..88627238) | | |
| ID: 127273971 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:88817505-88818005 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88517987..88518487) | | |
| ID: 127273970 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:88817004-88817504 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88517486..88517986) | | |
| ID: 127273969 | H3K4me1 hESC enhancer GRCh37_chr2:88811519-88812020 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88512001..88512502) | | |
| ID: 127273968 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:88743871-88744504 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88444352..88444985) | | |
| ID: 127273967 | OCT4-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:88743237-88743870 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88443718..88444351) | | |
| ID: 127273966 | H3K27ac hESC enhancer GRCh37_chr2:88741313-88741813 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88441794..88442294) | | |
| ID: 126806269 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:88899203-88900402 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88599685..88600884) | | |
| ID: 126806268 | MED14-independent group 3 enhancer GRCh37_chr2:88837459-88838658 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88537941..88539140) | | |
| ID: 126806267 | MED14-independent group 3 enhancer GRCh37_chr2:88803591-88804790 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88504073..88505272) | | |
| ID: 107985813 | RPL38 pseudogene 6 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88428075..88428620) | | |
| ID: 101928403 | EIF2AK3 divergent transcript [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88627829..88631825) | | |
| ID: 101928371 | uncharacterized LOC101928371 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88538720..88575610) | | |
| ID: 344167 | forkhead box I3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88446787..88452693, complement) | CFM2 | 612351 |
| ID: 200523 | sperm microtubule inner protein 9 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88524649..88529585) | C2orf51, TEX37, TSC21 | 619676 |
| ID: 9451 | eukaryotic translation initiation factor 2 alpha kinase 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (88556741..88628145, complement) | PEK, PERK, WRS | 604032 |