| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112637375-112637572 | Common:6; Rare:106 | ||||
| chr4:113116739-113117210 | Common:4; Rare:129 | ||||
| chr4:113145520-113145851 | Rare:59 | ||||
| chr4:113761106-113761531 | Common:6; Rare:198 | ||||
| chr4:113761708-113761966 | Common:2; Rare:116 | ||||
| chr4:118685260-118685450 | Common:6; Rare:118 | ||||
| chr4:118835938-118836267 | Common:5; Rare:128 | ||||
| chr4:119212351-119212779 | Common:9; Rare:251 | ||||
| chr4:119300470-119301140 | Common:4; Rare:407 | ||||
| chr4:120066747-120067008 | Common:10; Rare:153 | ||||
| chr4:121696873-121697226 | Common:11; Rare:195 | ||||
| chr4:121801233-121801411 | Common:4; Rare:122 | ||||
| chr4:121823824-121824110 | Common:3; Rare:130 | ||||
| chr4:122152233-122152429 | Common:4; Rare:164 | ||||
| chr4:122732445-122732824 | Common:4; Rare:230; Clinvar:6; Clinvar (benign):4 |