ID: 129992954 | ATAC-STARR-seq lymphoblastoid active region 21808 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109815138..109815237) | | |
ID: 129992953 | ATAC-STARR-seq lymphoblastoid silent region 15626 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109729859..109730198) | | |
ID: 129992952 | ATAC-STARR-seq lymphoblastoid active region 21807 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109729459..109729528) | | |
ID: 129992951 | ATAC-STARR-seq lymphoblastoid active region 21806 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109703817..109703866) | | |
ID: 129992950 | ATAC-STARR-seq lymphoblastoid silent region 15625 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109703367..109703656) | | |
ID: 129992949 | ATAC-STARR-seq lymphoblastoid silent region 15624 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109703107..109703216) | | |
ID: 129992948 | ATAC-STARR-seq lymphoblastoid active region 21805 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109702867..109702926) | | |
ID: 129992947 | ATAC-STARR-seq lymphoblastoid active region 21804 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109702047..109702106) | | |
ID: 129992946 | ATAC-STARR-seq lymphoblastoid active region 21803 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109560933..109561132) | | |
ID: 129992945 | ATAC-STARR-seq lymphoblastoid silent region 15623 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109560193..109560512) | | |
ID: 129661318 | ReSE screen-validated silencer GRCh37_chr4:110487413-110487630 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109566257..109566474) | | |
ID: 127401333 | H3K27ac hESC enhancer GRCh37_chr4:110651344-110652220 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109730188..109731064) | | |
ID: 127401332 | NANOG hESC enhancer GRCh37_chr4:110537978-110538479 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109616822..109617323) | | |
ID: 124900758 | GAR1 divergent transcript [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109812919..109815382, complement) | | |
ID: 124900755 | uncharacterized LOC124900755 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109613511..109619117, complement) | | |
ID: 100874455 | HIG1 hypoxia inducible domain family member 1A pseudogene 14 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109673779..109674321) | | |
ID: 100131440 | CDC42 pseudogene 4 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109555108..109555813) | | |
ID: 81579 | phospholipase A2 group XIIA [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109709989..109730070, complement) | GXII, PLA2G12, ROSSY | 611652 |
ID: 55013 | mitochondrial calcium uniporter dominant negative subunit beta [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109560246..109688719) | CCDC109B | 620702 |
ID: 3426 | complement factor I [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109730982..109801999, complement) | AHUS3, ARMD13, C3BINA, C3b-INA, FI, IF, KAF | 217030 |