| ID: 127406962 | NANOG hESC enhancer GRCh37_chr6:107033226-107033920 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106585351..106586045) | | |
| ID: 127406961 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:107023180-107023700 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106575305..106575825) | | |
| ID: 127406960 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:106959060-106960018 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106511185..106512143) | | |
| ID: 127406959 | H3K4me1 hESC enhancer GRCh37_chr6:106957727-106958332 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106509846..106510457) | | |
| ID: 127406958 | OCT4-NANOG hESC enhancer GRCh37_chr6:106908781-106909430 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106460906..106461555) | | |
| ID: 127406957 | H3K27ac hESC enhancer GRCh37_chr6:106895745-106896246 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106447870..106448371) | | |
| ID: 127406956 | H3K4me1 hESC enhancer GRCh37_chr6:106808598-106809464 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106360723..106361589) | | |
| ID: 127406955 | H3K27ac hESC enhancer GRCh37_chr6:106771297-106771797 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106323422..106323922) | | |
| ID: 127406954 | H3K27ac hESC enhancer GRCh37_chr6:106770796-106771296 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106322921..106323421) | | |
| ID: 126859757 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr6:106967140-106968339 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106519265..106520464) | | |
| ID: 105377924 | uncharacterized LOC105377924 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106451496..106457248, complement) | | |
| ID: 101927405 | uncharacterized LOC101927405 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106491245..106502221, complement) | | |
| ID: 100873471 | RNA, 5S ribosomal pseudogene 211 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106449381..106449497) | RN5S211 | |
| ID: 84816 | reticulon 4 interacting protein 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106570771..106630491, complement) | NIMP, OPA10 | 610502 |
| ID: 9474 | autophagy related 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106184476..106325760, complement) | APG5, APG5-LIKE, APG5L, ASP, SCAR25, hAPG5 | 604261 |
| ID: 202 | crystallin beta-gamma domain containing 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (106360717..106572017) | AIM1, ST4 | 601797 |