Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:143060742-143060919 | Common:7; Rare:61 | ||||
chr6:143450660-143450936 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
chr6:143843128-143843402 | Common:2; Rare:91 | ||||
chr6:144285223-144285335 | Common:1; Rare:31 | ||||
chr6:145814731-145814903 | Common:1; Rare:86 | ||||
chr6:149546010-149546173 | Common:1; Rare:72 | ||||
chr6:149718058-149718151 | Common:1; Rare:30 | ||||
chr6:149749523-149749796 | Rare:122 | ||||
chr6:151452022-151452552 | Common:5; Rare:189; Clinvar (benign):3 | ||||
chr6:152983508-152983737 | Common:3; Rare:86 | ||||
chr6:153002652-153003043 | Common:5; Rare:128 | ||||
chr6:153131225-153131498 | Rare:124 | ||||
chr6:154995215-154995318 | Rare:30 | ||||
chr6:158168201-158168388 | Common:2; Rare:66 | ||||
chr6:158644704-158645067 | Common:2; Rare:117 |