| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:109980466-109980720 | Common:2; Rare:39 | ||||
| chr4:112231585-112231844 | Common:2; Rare:80 | ||||
| chr4:112285682-112285981 | Common:1; Rare:91 | ||||
| chr4:112636860-112637218 | Common:2; Rare:101 | ||||
| chr4:112646205-112646432 | Rare:83; Clinvar:1 | ||||
| chr4:113761002-113761286 | Common:1; Rare:78 | ||||
| chr4:113761460-113761507 | Rare:17 | ||||
| chr4:113761698-113761814 | Common:1; Rare:36 | ||||
| chr4:113979201-113979326 | Common:1; Rare:22 | ||||
| chr4:113979527-113979855 | Common:6; Rare:74 | ||||
| chr4:117085478-117085615 | Common:1; Rare:39 | ||||
| chr4:118352193-118352577 | Common:1; Rare:149; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:118352709-118352868 | Common:2; Rare:56; Clinvar (benign):1 | ||||
| chr4:118352972-118353053 | Rare:29 | ||||
| chr4:118685314-118685534 | Common:2; Rare:62 |