ID: 130068641 | ATAC-STARR-seq lymphoblastoid silent region 20978 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129678375..129678554) | | |
ID: 130068640 | ATAC-STARR-seq lymphoblastoid active region 29918 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129677975..129678144) | | |
ID: 130068639 | ATAC-STARR-seq lymphoblastoid active region 29917 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129656080..129656139) | | |
ID: 130068638 | ATAC-STARR-seq lymphoblastoid active region 29916 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129655980..129656069) | | |
ID: 130068637 | ATAC-STARR-seq lymphoblastoid silent region 20977 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129654718..129654797) | | |
ID: 130068636 | ATAC-STARR-seq lymphoblastoid silent region 20976 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129654578..129654627) | | |
ID: 130068635 | ATAC-STARR-seq lymphoblastoid active region 29915 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129654228..129654287) | | |
ID: 130068634 | ATAC-STARR-seq lymphoblastoid silent region 20975 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129637602..129637771) | | |
ID: 127898272 | H3K4me1 hESC enhancer GRCh37_chrX:128783931-128784430 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129649954..129650453) | | |
ID: 127898271 | H3K4me1 hESC enhancer GRCh37_chrX:128783429-128783930 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129649452..129649953) | | |
ID: 127898270 | H3K4me1 hESC enhancer GRCh37_chrX:128735069-128735569 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129601092..129601592) | | |
ID: 127898269 | H3K4me1 hESC enhancer GRCh37_chrX:128734568-128735068 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129600591..129601091) | | |
ID: 127898268 | NANOG hESC enhancer GRCh37_chrX:128698883-128699384 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129564906..129565407) | | |
ID: 124900503 | small nucleolar RNA SNORD112 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129518576..129518647) | | |
ID: 113875009 | Sharpr-MPRA regulatory region 14523 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129666332..129666626) | | |
ID: 113875008 | Sharpr-MPRA regulatory region 13828 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129540092..129540472) | | |
ID: 105373334 | uncharacterized LOC105373334 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129675888..129678470, complement) | | |
ID: 100873564 | RNA, 5S ribosomal pseudogene 513 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129436530..129436647, complement) | RN5S513 | |
ID: 8862 | apelin [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129645259..129654956, complement) | APEL, XNPEP2 | 300297 |
ID: 6594 | SNF2 related chromatin remodeling ATPase 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129446506..129523490, complement) | ISWI, NURF140, SNF2L, SNF2L1, SNF2LB, SNF2LT, SWI, SWI2, hSNF2L | 300012 |