ID: 129999182 | ATAC-STARR-seq lymphoblastoid silent region 18569 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117012076..117012125) | | |
ID: 129999181 | ATAC-STARR-seq lymphoblastoid active region 26540 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117011006..117011085) | | |
ID: 129999180 | ATAC-STARR-seq lymphoblastoid silent region 18568 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116963359..116963408) | | |
ID: 129999179 | ATAC-STARR-seq lymphoblastoid silent region 18567 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116955854..116956113) | | |
ID: 129999178 | ATAC-STARR-seq lymphoblastoid silent region 18564 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116953417..116953486) | | |
ID: 129999177 | ATAC-STARR-seq lymphoblastoid active region 26539 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116953047..116953156) | | |
ID: 127457476 | NANOG hESC enhancer GRCh37_chr7:116609424-116609981 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116969370..116969927) | | |
ID: 127457475 | H3K27ac hESC enhancer GRCh37_chr7:116593626-116594549 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116953572..116954495) | | |
ID: 126860159 | MED14-independent group 3 enhancer GRCh37_chr7:116659304-116660503 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117019250..117020449) | | |
ID: 124901857 | uncharacterized LOC124901857 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116903318..116903443) | | |
ID: 123956215 | Sharpr-MPRA regulatory region 2110 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116928895..116929189) | | |
ID: 116186911 | CRISPRi-validated cis-regulatory element chr7.4218 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116950058..116950383) | | |
ID: 113219444 | greater CFTR locus negative regulatory element CR9 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116918230..116918944) | | |
ID: 105375465 | uncharacterized LOC105375465 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116940339..116947917) | | |
ID: 102466616 | microRNA 6132 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117020211..117020319) | hsa-mir-6132 | |
ID: 100873497 | RNA, 5S ribosomal pseudogene 239 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116944286..116944414, complement) | RN5S239 | |
ID: 338069 | ST7 overlapping transcript 4 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116953848..116959817) | NCRNA00042, ST7OT4 | |
ID: 252956 | tropomyosin 3 pseudogene 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116970897..116972985, complement) | TPM3L2 | |
ID: 93653 | ST7 antisense RNA 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116952446..116954334, complement) | ST7AS1, ST7OT1 | |
ID: 7982 | suppression of tumorigenicity 7 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116953501..117230176) | ETS7q, FAM4A, FAM4A1, HELG, RAY1, SEN4, TSG7 | 600833 |