Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:139453683-139453749 | Common:2; Rare:21 | ||||
chr4:139453774-139454185 | Common:3; Rare:104; Clinvar:10; Clinvar (benign):4 | ||||
chr4:139556103-139556567 | Rare:96 | ||||
chr4:140373377-140373709 | Common:3; Rare:135 | ||||
chr4:143184661-143185169 | Common:8; Rare:189 | ||||
chr4:143185237-143185425 | Rare:56 | ||||
chr4:143185579-143185852 | Common:2; Rare:68 | ||||
chr4:145098141-145098361 | Rare:77 | ||||
chr4:145619232-145619402 | Rare:67 | ||||
chr4:147684098-147684271 | Common:1; Rare:66 | ||||
chr4:148442355-148442712 | Rare:103; Clinvar:4; Clinvar (benign):3 | ||||
chr4:151015220-151015364 | Rare:40 | ||||
chr4:151099473-151099709 | Common:3; Rare:95 | ||||
chr4:151409116-151409452 | Common:4; Rare:76 | ||||
chr4:152779636-152780169 | Common:3; Rare:131 |