ID: 129998228 | ATAC-STARR-seq lymphoblastoid active region 25835 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33129517..33129626) | | |
ID: 129998227 | ATAC-STARR-seq lymphoblastoid silent region 18091 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33129167..33129466) | | |
ID: 129998226 | ATAC-STARR-seq lymphoblastoid active region 25834 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33128977..33129026) | | |
ID: 129998225 | ATAC-STARR-seq lymphoblastoid silent region 18090 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33109300..33109779) | | |
ID: 129998224 | ATAC-STARR-seq lymphoblastoid silent region 18089 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33109060..33109289) | | |
ID: 129998223 | ATAC-STARR-seq lymphoblastoid active region 25833 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33063131..33063290) | | |
ID: 129998222 | ATAC-STARR-seq lymphoblastoid silent region 18088 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33062771..33062890) | | |
ID: 129998221 | ATAC-STARR-seq lymphoblastoid silent region 18087 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33062411..33062470) | | |
ID: 129998220 | ATAC-STARR-seq lymphoblastoid silent region 18086 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33044200..33044359) | | |
ID: 129998219 | ATAC-STARR-seq lymphoblastoid silent region 18085 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33040928..33041027) | | |
ID: 127408855 | NANOG-H3K27ac hESC enhancer GRCh37_chr7:33391529-33392028 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33351917..33352416) | | |
ID: 127408854 | NANOG-H3K27ac hESC enhancer GRCh37_chr7:33391027-33391528 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33351415..33351916) | | |
ID: 126859988 | MED14-independent group 3 enhancer GRCh37_chr7:33327115-33328314 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33287503..33288702) | | |
ID: 124901610 | uncharacterized LOC124901610 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33063185..33095399) | | |
ID: 106481758 | RNA, 7SL, cytoplasmic 505, pseudogene [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33045798..33046090, complement) | | |
ID: 100873487 | RNA, 5S ribosomal pseudogene 229 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33177740..33177838) | RN5S229 | |
ID: 100421336 | RAB3A interacting protein like 1 pseudogene [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33379949..33380866) | | |
ID: 100129599 | ribosomal protein S29 pseudogene 14 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33036212..33036382, complement) | RPS29_3_802 | |
ID: 51251 | 5'-nucleotidase, cytosolic IIIA [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33014113..33062776, complement) | CNSHA8, NT5C3, P5'N-1, P5N-1, PN-I, POMP, PSN1, UMPH, UMPH1, cN-III, hUMP1, p36 | 606224 |
ID: 27241 | Bardet-Biedl syndrome 9 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33129285..33635767) | B1, C18, D1, PTHB1 | 607968 |