ID: 127826342 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:52653792-52654549 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (52079656..52080413) | | |
ID: 127826341 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:52653033-52653791 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (52078897..52079655) | | |
ID: 124900147 | Sharpr-MPRA regulatory region 15635 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51996033..51996327) | | |
ID: 729163 | fatty acid binding protein 5 pseudogene 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51966682..51967340) | FABP5L2 | |
ID: 440138 | ALG11 alpha-1,2-mannosyltransferase [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (52012398..52033600) | CDG1P, GT8 | 613666 |
ID: 341676 | NIMA related kinase 5 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (52033611..52129073, complement) | | 616731 |
ID: 9724 | UTP14C small subunit processome component [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (52024691..52033600) | 2700066J21Rik, KIAA0266, UTP14B | 608969 |
ID: 540 | ATPase copper transporting beta [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (51932669..52012132, complement) | PWD, WC1, WD, WND | 606882 |