Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:143060724-143060919 | Common:7; Rare:67 | ||||
chr6:151452117-151452352 | Common:2; Rare:71 | ||||
chr6:158168233-158168388 | Common:2; Rare:56 | ||||
chr6:159727039-159727155 | Rare:38 | ||||
chr6:159789567-159789947 | Common:2; Rare:131 | ||||
chr6:166342526-166342638 | Common:2; Rare:43 | ||||
chr7:2242178-2242256 | Common:2; Rare:46 | ||||
chr7:6009050-6009350 | Common:4; Rare:121; Clinvar:1; Clinvar (benign):7 | ||||
chr7:16645843-16646156 | Common:2; Rare:103 | ||||
chr7:30594761-30594942 | Common:2; Rare:90; Clinvar:5; Clinvar (benign):5 | ||||
chr7:32495264-32495542 | Rare:72 | ||||
chr7:40134833-40135018 | Rare:66; Clinvar:1 | ||||
chr7:42932164-42932389 | Rare:84 | ||||
chr7:44044597-44044740 | Common:2; Rare:36 | ||||
chr7:44490604-44490852 | Rare:79 |