ID: 132090194 | Neanderthal introgressed variant-containing enhancer experimental_32874 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41521004..41521173) | | |
ID: 130009633 | ATAC-STARR-seq lymphoblastoid active region 7632 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41465212..41465471) | | |
ID: 130009632 | ATAC-STARR-seq lymphoblastoid active region 7631 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41463373..41463432) | | |
ID: 130009631 | ATAC-STARR-seq lymphoblastoid active region 7630 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41461840..41461939) | | |
ID: 130009630 | ATAC-STARR-seq lymphoblastoid active region 7629 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41458463..41458592) | | |
ID: 129663340 | ReSE screen-validated silencer GRCh37_chr13:42127997-42128188 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41553861..41554052) | | |
ID: 129663339 | ReSE screen-validated silencer GRCh37_chr13:42038640-42038854 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41464504..41464718) | | |
ID: 127826174 | NANOG-H3K4me1 hESC enhancer GRCh37_chr13:42114123-42114643 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41539987..41540507) | | |
ID: 127826173 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:42031872-42032549 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41457323..41458413) | | |
ID: 105370175 | uncharacterized LOC105370175 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41546886..41552202, complement) | | |
ID: 105370174 | uncharacterized LOC105370174 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41517168..41564091) | | |
ID: 100847026 | microRNA 5006 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41568286..41568395, complement) | | |
ID: 100506759 | olfactory receptor family 7 subfamily E member 37 pseudogene [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41442564..41443766) | OR7E48P, OST193, hg533 | |
ID: 100189007 | tRNA-Glu (CTC) 3-1 [Homo sapiens (human)] | | TRNAE4 | |
ID: 28984 | regulator of cell cycle [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41457550..41470871) | C13orf15, RGC-32, RGC32, bA157L14.2 | 610077 |
ID: 23078 | von Willebrand factor A domain containing 8 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41566835..41961109, complement) | KIAA0564, P7BP2, RP97 | 617509 |