| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:118836040-118836227 | Common:1; Rare:42 | ||||
| chr4:119212351-119212867 | Common:5; Rare:146 | ||||
| chr4:119213090-119213251 | Rare:25 | ||||
| chr4:120066748-120066904 | Common:1; Rare:51 | ||||
| chr4:120922649-120922766 | Rare:23; Clinvar:2 | ||||
| chr4:120922781-120922944 | Rare:56; Clinvar:2 | ||||
| chr4:121696862-121697057 | Common:5; Rare:49 | ||||
| chr4:121801237-121801422 | Common:2; Rare:61 | ||||
| chr4:121823415-121823740 | Rare:100 | ||||
| chr4:122732429-122732818 | Common:2; Rare:121; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122922554-122922812 | Common:3; Rare:93 | ||||
| chr4:122922897-122923152 | Common:2; Rare:76; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:127880764-127880947 | Rare:65 | ||||
| chr4:127965920-127965995 | Rare:14 | ||||
| chr4:128287350-128287632 | Common:1; Rare:95 |