ID: 132090195 | Neanderthal introgressed variant-containing enhancer experimental_32930 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51771416..51771585) | | |
ID: 130009837 | ATAC-STARR-seq lymphoblastoid active region 7784 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51945501..51945600) | | |
ID: 130009836 | ATAC-STARR-seq lymphoblastoid active region 7783 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51945371..51945440) | | |
ID: 130009835 | ATAC-STARR-seq lymphoblastoid active region 7782 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51804914..51805043) | | |
ID: 130009834 | ATAC-STARR-seq lymphoblastoid silent region 5377 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51803724..51804363) | | |
ID: 130009833 | ATAC-STARR-seq lymphoblastoid active region 7781 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51802479..51802528) | | |
ID: 130009832 | ATAC-STARR-seq lymphoblastoid active region 7780 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51797652..51797731) | | |
ID: 130009831 | ATAC-STARR-seq lymphoblastoid active region 7779 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51793788..51794147) | | |
ID: 130009830 | ATAC-STARR-seq lymphoblastoid silent region 5376 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51781498..51781547) | | |
ID: 130009829 | ATAC-STARR-seq lymphoblastoid active region 7778 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51764521..51764840) | | |
ID: 127826340 | H3K4me1 hESC enhancer GRCh37_chr13:52423314-52423814 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51849178..51849678) | | |
ID: 127826339 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:52371189-52371717 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51797053..51797581) | | |
ID: 126861781 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr13:52501865-52503064 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51927729..51928928) | | |
ID: 126861780 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr13:52435707-52436906 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51861571..51862770) | | |
ID: 124903177 | uncharacterized LOC124903177 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51722253..51739098, complement) | | |
ID: 107984561 | uncharacterized LOC107984561 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51803836..51813832) | | |
ID: 729163 | fatty acid binding protein 5 pseudogene 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51966682..51967340) | FABP5L2 | |
ID: 283521 | transmembrane protein 272 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51813347..51934366, complement) | LINC00282, NCRNA00282 | |
ID: 220112 | CTAGE family member 3, pseudogene [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51907820..51910696, complement) | CTAGE-3, CTAGE3 | 608857 |
ID: 115825 | WD repeat and FYVE domain containing 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51584462..51767709) | PROF, WDF2, ZFYVE22 | 610418 |