| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112231586-112231831 | Common:2; Rare:76 | ||||
| chr4:112636844-112637197 | Common:1; Rare:97 | ||||
| chr4:112637394-112637570 | Common:3; Rare:47 | ||||
| chr4:113978953-113979203 | Common:3; Rare:39 | ||||
| chr4:113979602-113979840 | Common:6; Rare:53 | ||||
| chr4:117085525-117085581 | Common:1; Rare:17 | ||||
| chr4:118685235-118685421 | Common:2; Rare:59 | ||||
| chr4:118836043-118836257 | Common:2; Rare:49 | ||||
| chr4:119212355-119212738 | Common:4; Rare:118 | ||||
| chr4:120066754-120066955 | Common:3; Rare:62 | ||||
| chr4:120922834-120922944 | Rare:30; Clinvar:1 | ||||
| chr4:121696862-121697099 | Common:5; Rare:68 | ||||
| chr4:121801218-121801411 | Common:2; Rare:72 | ||||
| chr4:121823771-121824131 | Common:4; Rare:90 | ||||
| chr4:121870406-121870651 | Common:1; Rare:59; Clinvar (benign):1 |