ID: 130000750 | ATAC-STARR-seq lymphoblastoid active region 27632 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94553163..94553782) | | |
ID: 130000749 | ATAC-STARR-seq lymphoblastoid active region 27631 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94474848..94475077) | | |
ID: 130000748 | ATAC-STARR-seq lymphoblastoid silent region 19367 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94473330..94473379) | | |
ID: 130000747 | ATAC-STARR-seq lymphoblastoid silent region 19366 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94442437..94442506) | | |
ID: 130000746 | ATAC-STARR-seq lymphoblastoid active region 27630 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94440706..94441035) | | |
ID: 127459942 | H3K27ac hESC enhancer GRCh37_chr8:95546863-95547362 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94534635..94535134) | | |
ID: 127459941 | H3K27ac hESC enhancer GRCh37_chr8:95480885-95481510 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94468657..94469282) | | |
ID: 127459940 | H3K27ac hESC enhancer GRCh37_chr8:95480258-95480884 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94468030..94468656) | | |
ID: 127459939 | NANOG hESC enhancer GRCh37_chr8:95456748-95457280 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94444520..94445052) | | |
ID: 127459938 | NANOG-H3K27ac hESC enhancer GRCh37_chr8:95447028-95447528 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94434800..94435300) | | |
ID: 101926977 | VIRMA divergent transcript [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94553713..94570650) | | |
ID: 100861412 | fibrinogen silencer binding protein [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94427716..94436944, complement) | | 616306 |
ID: 100286997 | ribosomal protein L31 pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94565009..94565690) | | |
ID: 25962 | vir like m6A methyltransferase associated [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94487689..94553469, complement) | KIAA1429, MSTP054, fSAP121 | 616447 |
ID: 25788 | RAD54 homolog B [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94371960..94475115, complement) | RDH54 | 604289 |