ID: 130068044 | ATAC-STARR-seq lymphoblastoid silent region 20702 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (23318221..23318390) | | |
ID: 130068043 | ATAC-STARR-seq lymphoblastoid active region 29488 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (22192578..22192837) | | |
ID: 130068042 | ATAC-STARR-seq lymphoblastoid active region 29487 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (21993254..21993303) | | |
ID: 130068041 | ATAC-STARR-seq lymphoblastoid silent region 20701 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (21941162..21941391) | | |
ID: 130068040 | ATAC-STARR-seq lymphoblastoid silent region 20700 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (21940502..21940971) | | |
ID: 129664917 | ReSE screen-validated silencer GRCh37_chrX:23155798-23156034 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (23137681..23137917) | | |
ID: 129664916 | ReSE screen-validated silencer GRCh37_chrX:23111444-23111682 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (23093327..23093565) | | |
ID: 129664915 | ReSE screen-validated silencer GRCh37_chrX:22552803-22552990 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (22534686..22534873) | | |
ID: 127897298 | NANOG-H3K27ac hESC enhancer GRCh37_chrX:23523568-23524107 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (23505451..23505990) | | |
ID: 127897297 | NANOG-H3K27ac hESC enhancer GRCh37_chrX:23362831-23363330 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (23344714..23345213) | | |
ID: 127897296 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:23256953-23257600 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (23238836..23239483) | | |
ID: 127897295 | OCT4-NANOG hESC enhancer GRCh37_chrX:22463802-22464451 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (22445685..22446334) | | |
ID: 126863227 | CDK7 strongly-dependent group 2 enhancer GRCh37_chrX:22968225-22969424 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (22950108..22951307) | | |
ID: 126863226 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chrX:22544316-22545515 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (22526199..22527398) | | |
ID: 126863225 | CDK7 strongly-dependent group 2 enhancer GRCh37_chrX:22450970-22452169 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (22432853..22434052) | | |
ID: 126863224 | CDK7 strongly-dependent group 2 enhancer GRCh37_chrX:22417737-22418936 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (22399620..22400819) | | |
ID: 126863223 | CDK7 strongly-dependent group 2 enhancer GRCh37_chrX:22383141-22384340 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (22365024..22366223) | | |
ID: 124905276 | small nucleolar RNA U13 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (23507211..23507313, complement) | | |
ID: 106479684 | RNA, U6 small nuclear 266, pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (22527835..22527941) | | |
ID: 100873942 | PHEX antisense RNA 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (22162732..22172983, complement) | | |