ID: 129661379 | ReSE screen-validated silencer GRCh37_chr4:190937742-190937939 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (190016587..190016784) | | |
ID: 129661378 | ReSE screen-validated silencer GRCh37_chr4:190896381-190896551 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189975226..189975396) | | |
ID: 127402143 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:190942591-190943245 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (190021436..190022090) | | |
ID: 127402142 | H3K27ac hESC enhancer GRCh37_chr4:190862333-190862832 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189941178..189941677) | | |
ID: 123493255 | Sharpr-MPRA regulatory region 15710 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189988174..189988468) | | |
ID: 106480758 | RNA, 5S ribosomal pseudogene 175 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (190017696..190017814) | RN5S175 | |
ID: 106480724 | MLLT10 pseudogene 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189973599..189973847, complement) | | |
ID: 106478998 | RNA, 5S ribosomal pseudogene 174 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (190015138..190015255) | RN5S174 | |
ID: 100288711 | double homeobox 4 like 9 (pseudogene) [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (190021169..190022665, complement) | DUX4C | 615581 |
ID: 100132380 | angiogenic factor with G-patch and FHA domains 1 pseudogene 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (190040990..190044286) | | |
ID: 728339 | FRG1 divergent transcript [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189764391..189940733, complement) | | |
ID: 644881 | retinoic acid receptor responder 2 pseudogene 4 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (190037796..190038423, complement) | | |
ID: 448831 | FSHD region gene 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (190024367..190027256, complement) | FRG2A | 609032 |
ID: 56604 | tubulin beta 7 pseudogene [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189982335..189984929, complement) | TUBB4Q | |
ID: 2483 | FSHD region gene 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189940872..189963192) | FRG1A, FSG1 | 601278 |