Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:139301299-139301571 | Common:3; Rare:88 | ||||
chr4:139453693-139453726 | Common:2; Rare:8 | ||||
chr4:139453945-139454241 | Common:3; Rare:94; Clinvar:5; Clinvar (benign):4 | ||||
chr4:140373358-140373696 | Common:2; Rare:133 | ||||
chr4:143184657-143185068 | Common:8; Rare:153 | ||||
chr4:145098148-145098350 | Rare:71 | ||||
chr4:145619334-145619396 | Rare:24 | ||||
chr4:147617242-147617503 | Common:1; Rare:58 | ||||
chr4:147684106-147684265 | Common:1; Rare:60 | ||||
chr4:148442355-148442712 | Rare:103; Clinvar:4; Clinvar (benign):3 | ||||
chr4:151100200-151100580 | Common:1; Rare:72 | ||||
chr4:151408874-151409446 | Common:7; Rare:156 | ||||
chr4:152382500-152382642 | Common:1; Rare:19 | ||||
chr4:152679896-152680156 | Rare:79 | ||||
chr4:152779730-152780031 | Common:1; Rare:86 |