| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:119454556-119454986 | Common:18; Rare:137 | ||||
| chr4:124020161-124020385 | Common:1; Rare:40 | ||||
| chr4:137700841-137701037 | Common:2; Rare:33 | ||||
| chr4:143336024-143336166 | Rare:42 | ||||
| chr4:143559387-143559487 | Common:1; Rare:30 | ||||
| chr4:147733807-147733907 | Rare:14 | ||||
| chr4:151176562-151176943 | Common:1; Rare:44 | ||||
| chr4:153684155-153684324 | Rare:54 | ||||
| chr4:154004955-154005187 | Common:1; Rare:46 | ||||
| chr4:154998557-154998756 | Common:1; Rare:29 | ||||
| chr4:168903618-168903881 | Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:168915768-168915932 | Common:1; Rare:38; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:168924139-168924413 | Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:173416189-173416469 | Common:3; Rare:45 | ||||
| chr4:173509555-173509675 | Common:1; Rare:34 |