| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:118888733-118888961 | Common:1; Rare:60 | ||||
| chr4:119212536-119212730 | Common:2; Rare:51 | ||||
| chr4:120066831-120066964 | Common:4; Rare:33 | ||||
| chr4:121696862-121697130 | Common:5; Rare:73 | ||||
| chr4:121801252-121801407 | Common:2; Rare:48 | ||||
| chr4:121823869-121824121 | Common:2; Rare:64 | ||||
| chr4:122152261-122152390 | Common:2; Rare:59 | ||||
| chr4:122732436-122732791 | Common:2; Rare:112; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122922988-122923113 | Common:1; Rare:36 | ||||
| chr4:123396783-123396860 | Rare:25 | ||||
| chr4:123398274-123398488 | Common:1; Rare:74 | ||||
| chr4:127880803-127880934 | Rare:43 | ||||
| chr4:127965896-127965926 | Common:1; Rare:4; Clinvar (benign):1 | ||||
| chr4:129093422-129093741 | Common:2; Rare:90 | ||||
| chr4:133149103-133149301 | Common:2; Rare:60 |