ID: 130063144 | ATAC-STARR-seq lymphoblastoid silent region 9846 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3485150..3485199) | | |
ID: 130063143 | ATAC-STARR-seq lymphoblastoid silent region 9845 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3485090..3485139) | | |
ID: 130063142 | ATAC-STARR-seq lymphoblastoid silent region 9844 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3457529..3457578) | | |
ID: 129391027 | MPRA-validated peak3246 silencer [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3464062..3464262) | | |
ID: 127890043 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:3483217-3483755 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3483219..3483757) | | |
ID: 127890042 | H3K4me1 hESC enhancer GRCh37_chr19:3465691-3466191 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3465693..3466193) | | |
ID: 127890041 | H3K4me1 hESC enhancer GRCh37_chr19:3465190-3465690 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3465192..3465692) | | |
ID: 127890040 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:3463073-3463608 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3463075..3463610) | | |
ID: 127890039 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:3462537-3463072 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3462539..3463074) | | |
ID: 125371452 | Sharpr-MPRA regulatory region 13615 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3467771..3468065) | | |
ID: 122405565 | small integral membrane protein 44 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3482110..3483441, complement) | CTF5, NFI1_HUMAN, NFI2_HUMAN, NFIC | |
ID: 105372246 | uncharacterized LOC105372246 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3482978..3491361) | | |
ID: 284422 | small integral membrane protein 24 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3473986..3480525, complement) | C19orf77, HSPC323, MARDI | |
ID: 83475 | deoxyhypusine hydroxylase [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3490824..3500674, complement) | HLRC1, NEDMVIC, hDOHH | 611262 |
ID: 4782 | nuclear factor I C [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3359630..3469217) | CTF, CTF5, NF-I, NFI | 600729 |