| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:120066775-120066964 | Common:4; Rare:54 | ||||
| chr4:121696862-121697132 | Common:5; Rare:74 | ||||
| chr4:121823858-121824116 | Common:2; Rare:67 | ||||
| chr4:122732435-122732768 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922994-122923147 | Common:1; Rare:56; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:127880764-127880947 | Rare:65 | ||||
| chr4:127965896-127965923 | Common:1; Rare:3; Clinvar (benign):1 | ||||
| chr4:128061002-128061329 | Common:1; Rare:116 | ||||
| chr4:128287773-128288015 | Common:3; Rare:93 | ||||
| chr4:128288197-128288341 | Common:5; Rare:55 | ||||
| chr4:129093401-129093741 | Common:2; Rare:95 | ||||
| chr4:139301177-139301562 | Common:6; Rare:106 | ||||
| chr4:139302443-139302541 | Rare:24 | ||||
| chr4:139453683-139454204 | Common:5; Rare:143; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556397-139556611 | Rare:32 |