| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112285745-112285978 | Rare:73 | ||||
| chr4:112636869-112637187 | Common:1; Rare:89 | ||||
| chr4:112637390-112637570 | Common:3; Rare:47 | ||||
| chr4:112817977-112818181 | Rare:26 | ||||
| chr4:113292567-113292861 | Common:2; Rare:56 | ||||
| chr4:113293077-113293515 | Common:1; Rare:94; Clinvar:2; Clinvar (benign):3 | ||||
| chr4:113317280-113317579 | Common:2; Rare:45 | ||||
| chr4:113317681-113317743 | Rare:11; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:113761129-113761243 | Common:1; Rare:28 | ||||
| chr4:113979056-113979246 | Common:2; Rare:33 | ||||
| chr4:113979582-113979837 | Common:6; Rare:60 | ||||
| chr4:118685318-118685560 | Common:2; Rare:68 | ||||
| chr4:118836014-118836224 | Common:1; Rare:45 | ||||
| chr4:119212355-119212812 | Common:5; Rare:136 | ||||
| chr4:119213072-119213327 | Rare:43 |