| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112285851-112286024 | Rare:51 | ||||
| chr4:112636898-112637187 | Common:1; Rare:78 | ||||
| chr4:112637389-112637570 | Common:3; Rare:47 | ||||
| chr4:113978946-113979203 | Common:3; Rare:41 | ||||
| chr4:113979602-113979665 | Common:1; Rare:14 | ||||
| chr4:113979668-113979699 | Rare:4 | ||||
| chr4:113979711-113979817 | Common:5; Rare:24 | ||||
| chr4:118685318-118685471 | Common:2; Rare:48 | ||||
| chr4:118835952-118836208 | Common:1; Rare:57 | ||||
| chr4:119212341-119212677 | Common:2; Rare:104 | ||||
| chr4:120066764-120066955 | Common:3; Rare:56 | ||||
| chr4:121696862-121697192 | Common:5; Rare:93 | ||||
| chr4:121801246-121801405 | Common:2; Rare:51 | ||||
| chr4:122732436-122732768 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922933-122923137 | Common:2; Rare:62 |