ID: 130063936 | ATAC-STARR-seq lymphoblastoid active region 14271 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17406592..17406641) | | |
ID: 130063935 | ATAC-STARR-seq lymphoblastoid active region 14270 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17406342..17406391) | | |
ID: 130063934 | ATAC-STARR-seq lymphoblastoid active region 14269 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17406232..17406291) | | |
ID: 130063933 | ATAC-STARR-seq lymphoblastoid active region 14268 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17405662..17406041) | | |
ID: 130063932 | ATAC-STARR-seq lymphoblastoid active region 14267 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17405532..17405591) | | |
ID: 130063931 | ATAC-STARR-seq lymphoblastoid silent region 10342 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17391330..17391519) | | |
ID: 130063930 | ATAC-STARR-seq lymphoblastoid silent region 10341 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17391080..17391319) | | |
ID: 129664386 | ReSE screen-validated silencer GRCh37_chr19:17513926-17514094 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17403117..17403285) | | |
ID: 127890781 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr19:17525723-17526510 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17414914..17415701) | | |
ID: 127890780 | H3K4me1 hESC enhancer GRCh37_chr19:17518151-17518677 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17407342..17407868) | | |
ID: 127890779 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:17515618-17516356 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17404809..17405547) | | |
ID: 127890778 | H3K4me1 hESC enhancer GRCh37_chr19:17489969-17490857 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17379160..17380048) | | |
ID: 116276507 | CRISPRi-validated cis-regulatory element chr19.2705 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17398976..17399540) | | |
ID: 110806280 | coiled-coil domain containing 194 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17387196..17394196, complement) | | |
ID: 105372298 | uncharacterized LOC105372298 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17378790..17379772, complement) | | |
ID: 105221694 | BST2 interferon stimulated positive regulator [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17405686..17415736) | lncBST2 | |
ID: 100420015 | high mobility group box 3 pseudogene 29 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17417031..17418288, complement) | | |
ID: 93343 | multivesicular body subunit 12A [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17405741..17425332) | CFBP, FAM125A | |
ID: 684 | bone marrow stromal cell antigen 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17402939..17405630, complement) | CD317, HM1.24, TETHERIN | 600534 |