| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:113049455-113049684 | Common:1; Rare:39 | ||||
| chr4:113761174-113761276 | Common:1; Rare:24 | ||||
| chr4:117085482-117085633 | Common:1; Rare:42 | ||||
| chr4:118685235-118685535 | Common:3; Rare:88 | ||||
| chr4:118836036-118836234 | Common:1; Rare:43 | ||||
| chr4:118888753-118888976 | Common:1; Rare:59 | ||||
| chr4:119212384-119212757 | Common:4; Rare:111 | ||||
| chr4:119628773-119629106 | Common:8; Rare:138 | ||||
| chr4:120066418-120066473 | Rare:12 | ||||
| chr4:120066659-120066993 | Common:5; Rare:107 | ||||
| chr4:120922612-120922962 | Rare:105; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:121072246-121072439 | Rare:51 | ||||
| chr4:121696937-121697139 | Common:4; Rare:56 | ||||
| chr4:121801195-121801445 | Common:3; Rare:94 | ||||
| chr4:121823415-121823525 | Rare:42 |