| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:118850607-118850779 | Rare:36 | ||||
| chr4:119212351-119212864 | Common:5; Rare:146 | ||||
| chr4:119627280-119627398 | Rare:32 | ||||
| chr4:119628009-119628099 | Rare:19 | ||||
| chr4:119628567-119628927 | Common:4; Rare:155 | ||||
| chr4:120066673-120066904 | Common:1; Rare:76 | ||||
| chr4:120066906-120066999 | Common:3; Rare:25 | ||||
| chr4:120922611-120922961 | Rare:105; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:120923031-120923206 | Rare:51 | ||||
| chr4:121696649-121697289 | Common:7; Rare:165 | ||||
| chr4:121801246-121801439 | Common:2; Rare:62 | ||||
| chr4:122152208-122152461 | Common:2; Rare:100 | ||||
| chr4:122732414-122732834 | Common:3; Rare:133; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122826365-122826895 | Common:3; Rare:162 | ||||
| chr4:122827001-122827362 | Common:1; Rare:117; Clinvar (benign):1 |