Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:145098165-145098357 | Rare:66 | ||||
chr4:145619346-145619396 | Rare:17 | ||||
chr4:147617243-147617444 | Common:1; Rare:45 | ||||
chr4:150581734-150582016 | Rare:58 | ||||
chr4:152679949-152680156 | Rare:41 | ||||
chr4:152779711-152780016 | Common:1; Rare:84 | ||||
chr4:158172631-158172708 | Rare:12 | ||||
chr4:158671859-158672326 | Common:5; Rare:110; Clinvar:2; Clinvar (benign):1 | ||||
chr4:169010245-169010459 | Common:1; Rare:62 | ||||
chr4:169620382-169620643 | Common:2; Rare:101 | ||||
chr4:173370696-173370986 | Common:2; Rare:74 | ||||
chr4:173530166-173530487 | Common:2; Rare:67 | ||||
chr4:174283649-174283953 | Common:1; Rare:58 | ||||
chr4:177442376-177442514 | Rare:83; Clinvar:2 | ||||
chr4:183504415-183504628 | Rare:81 |