Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:184808385-184808613 | Rare:47 | ||||
chr4:185143213-185143483 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):6 | ||||
chr4:185396561-185396845 | Rare:93 | ||||
chr4:185425870-185426245 | Common:3; Rare:113 | ||||
chr4:185471054-185471412 | Common:10; Rare:46 | ||||
chr4:186191460-186191807 | Common:6; Rare:114; Clinvar:2; Clinvar (benign):5 | ||||
chr4:189940588-189941000 | Common:15; Rare:137 | ||||
chr5:191263-191505 | Common:2; Rare:59 | ||||
chr5:218097-218415 | Common:4; Rare:128; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr5:443084-443287 | Common:10; Rare:95 | ||||
chr5:892621-892915 | Common:5; Rare:95 | ||||
chr5:1799771-1799988 | Common:8; Rare:102 | ||||
chr5:1801278-1801480 | Common:4; Rare:105; Clinvar:3; Clinvar (benign):2 | ||||
chr5:6378498-6378706 | Rare:83 | ||||
chr5:6449067-6449160 | Rare:14 |