| ID: 127401189 | OCT4-NANOG hESC enhancer GRCh37_chr4:92550289-92550831 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (91629138..91629680) | | |
| ID: 127401188 | H3K27ac hESC enhancer GRCh37_chr4:92547183-92548021 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (91626032..91626870) | | |
| ID: 127401187 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:92544662-92545502 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (91623511..91624351) | | |
| ID: 127401186 | NANOG hESC enhancer GRCh37_chr4:92371022-92371547 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (91449871..91450396) | | |
| ID: 127401185 | NANOG hESC enhancer GRCh37_chr4:92189716-92190272 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (91268565..91269121) | | |
| ID: 127401184 | OCT4-NANOG hESC enhancer GRCh37_chr4:92177098-92177736 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (91255947..91256585) | | |
| ID: 127401183 | OCT4-NANOG hESC enhancer GRCh37_chr4:92133114-92133732 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (91211963..91212581) | | |
| ID: 127401182 | OCT4-NANOG hESC enhancer GRCh37_chr4:92020560-92021363 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (91099409..91100212) | | |
| ID: 127401181 | NANOG-H3K27ac hESC enhancer GRCh37_chr4:91985765-91986264 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (91064614..91065113) | | |
| ID: 127401180 | OCT4-NANOG hESC enhancer GRCh37_chr4:91754616-91755534 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (90833465..90834383) | | |
| ID: 127401179 | OCT4-NANOG hESC enhancer GRCh37_chr4:91105702-91106205 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (90184551..90185054) | | |
| ID: 126807110 | BRD4-independent group 4 enhancer GRCh37_chr4:91525257-91526456 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (90604106..90605305) | | |
| ID: 124900733 | uncharacterized LOC124900733 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (91268585..91325201, complement) | | |
| ID: 121725178 | Sharpr-MPRA regulatory region 11449 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (90314983..90315372) | | |
| ID: 110121083 | VISTA enhancer hs1374 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (89995882..89999902) | | |
| ID: 106480476 | RN7SK pseudogene 248 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (90370123..90370427) | | |
| ID: 105377331 | uncharacterized LOC105377331 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (90039592..90074822, complement) | | |
| ID: 401145 | coiled-coil serine rich protein 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (90127394..91605295) | FAM190A | 618934 |
| ID: 7117 | TMSB4X pseudogene 8 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (90838496..90839112, complement) | TMSL3 | |