| ID: 127400607 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:41218499-41219313 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (41216482..41217296) | | |
| ID: 127400606 | OCT4-NANOG hESC enhancer GRCh37_chr4:41071796-41072346 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (41069779..41070329) | | |
| ID: 127400605 | H3K4me1 hESC enhancer GRCh37_chr4:41065688-41066188 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (41063671..41064171) | | |
| ID: 127400604 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:40968186-40969148 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (40966169..40967131) | | |
| ID: 127400603 | NANOG hESC enhancer GRCh37_chr4:40842967-40843468 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (40840950..40841451) | | |
| ID: 127400602 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:40837789-40838358 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (40835772..40836341) | | |
| ID: 127400601 | H3K27ac hESC enhancer GRCh37_chr4:40809683-40810183 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (40807666..40808166) | | |
| ID: 127400600 | NANOG hESC enhancer GRCh37_chr4:40700528-40701301 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (40698511..40699284) | | |
| ID: 126807042 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr4:41126569-41127768 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (41124552..41125751) | | |
| ID: 124900907 | small nucleolar RNA U13 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (40868864..40868970, complement) | | |
| ID: 123477732 | Sharpr-MPRA regulatory region 7650 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (40923832..40924126) | | |
| ID: 112942285 | H3K4me1 hESC enhancer GRCh37_chr4:40899403-40899903 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (40897386..40897886) | | |
| ID: 106481918 | RNA, U6 small nuclear 836, pseudogene [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (41084607..41084713) | | |
| ID: 106480647 | RNA, U6 small nuclear 1195, pseudogene [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (41113942..41114044) | | |
| ID: 101410542 | UCHL1 divergent transcript [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (41220074..41256727, complement) | UCH1LAS, UCHL1-AS1 | 614991 |
| ID: 100873426 | RNA, 5S ribosomal pseudogene 160 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (40990154..40990273) | RN5S160 | |
| ID: 152709 | ADP ribosylation factor like GTPase 4A pseudogene 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (40785888..40787036) | ARL4P2 | |
| ID: 79730 | NOP2/Sun RNA methyltransferase family member 7 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (40749955..40811184) | | 617185 |
| ID: 323 | amyloid beta precursor protein binding family B member 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (40810027..41214542, complement) | FE65L, FE65L1 | 602710 |