| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:117085525-117085633 | Common:1; Rare:34 | ||||
| chr4:118352739-118353085 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr4:118685221-118685560 | Common:3; Rare:98 | ||||
| chr4:118836043-118836232 | Common:1; Rare:43 | ||||
| chr4:118838602-118838788 | Common:2; Rare:32 | ||||
| chr4:118888711-118889006 | Common:1; Rare:78 | ||||
| chr4:119212500-119212784 | Common:4; Rare:78 | ||||
| chr4:119213021-119213112 | Rare:22 | ||||
| chr4:119527253-119527339 | Rare:11 | ||||
| chr4:119627270-119627635 | Common:1; Rare:91 | ||||
| chr4:119627920-119628102 | Common:3; Rare:41 | ||||
| chr4:119628787-119629086 | Common:8; Rare:122 | ||||
| chr4:120066775-120066993 | Common:5; Rare:65 | ||||
| chr4:120922643-120923142 | Common:1; Rare:145; Clinvar:5 | ||||
| chr4:121696766-121697164 | Common:5; Rare:102 |