Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:122922935-122923137 | Common:2; Rare:62 | ||||
chr4:127965896-127965929 | Common:1; Rare:5; Clinvar (benign):1 | ||||
chr4:128061000-128061395 | Common:1; Rare:133 | ||||
chr4:128287789-128288016 | Common:3; Rare:88 | ||||
chr4:128288200-128288381 | Common:5; Rare:69 | ||||
chr4:128811222-128811317 | Rare:23 | ||||
chr4:129093431-129093736 | Common:2; Rare:85 | ||||
chr4:129096113-129096175 | Common:1; Rare:17 | ||||
chr4:139301209-139301543 | Common:6; Rare:94 | ||||
chr4:139302467-139302540 | Rare:12 | ||||
chr4:139453683-139454204 | Common:5; Rare:143; Clinvar:10; Clinvar (benign):4 | ||||
chr4:139556155-139556354 | Rare:45 | ||||
chr4:139665980-139666021 | Rare:14 | ||||
chr4:140373358-140373709 | Common:3; Rare:140 | ||||
chr4:140523938-140524224 | Common:2; Rare:86 |