ID: 130066218 | ATAC-STARR-seq lymphoblastoid active region 18145 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57351645..57351724) | | |
ID: 127893874 | H3K27ac hESC enhancer GRCh37_chr20:55925942-55926510 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57350886..57351454) | | |
ID: 127893873 | NANOG-H3K4me1 hESC enhancer GRCh37_chr20:55901895-55902397 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57326839..57327341) | | |
ID: 127893872 | NANOG-H3K4me1 hESC enhancer GRCh37_chr20:55901391-55901894 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57326335..57326838) | | |
ID: 127893871 | H3K4me1 hESC enhancer GRCh37_chr20:55892097-55892598 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57317041..57317542) | | |
ID: 127893870 | H3K4me1 hESC enhancer GRCh37_chr20:55876343-55876878 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57301287..57301822) | | |
ID: 127893869 | H3K4me1 hESC enhancer GRCh37_chr20:55867403-55867902 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57292347..57292846) | | |
ID: 127893868 | H3K4me1 hESC enhancer GRCh37_chr20:55865617-55866584 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57290561..57291528) | | |
ID: 127893867 | H3K4me1 hESC enhancer GRCh37_chr20:55862491-55862990 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57287435..57287934) | | |
ID: 127893866 | H3K4me1 hESC enhancer GRCh37_chr20:55861989-55862490 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57286933..57287434) | | |
ID: 112268270 | translation initiation factor IF-2-like [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57266440..57267287) | | |
ID: 109461473 | BMP7 promoter region [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57266129..57269490) | | |
ID: 105372687 | uncharacterized LOC105372687 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57274358..57329664, complement) | | |
ID: 100873221 | MT-ND1 pseudogene 9 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57357429..57358369, complement) | | |
ID: 100422883 | microRNA 4325 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57321502..57321591, complement) | | |
ID: 100271530 | ribosomal protein L39 pseudogene 39 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57328500..57328893) | RPL39_19_1716 | |
ID: 23626 | SPO11 initiator of meiotic double strand breaks [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57329803..57343993) | CT35, SPATA43, TOPOVIA, TOPVIA | 605114 |
ID: 8480 | ribonucleic acid export 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57351255..57379202) | Gle2, MIG14, MRNP41, Mnrp41, dJ481F12.3, dJ800J21.1 | 603343 |
ID: 655 | bone morphogenetic protein 7 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57168753..57266641, complement) | OP-1 | 112267 |