| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:109815464-109815786 | Common:1; Rare:88 | ||||
| chr4:112145316-112145649 | Common:1; Rare:89 | ||||
| chr4:112231597-112231972 | Common:3; Rare:105 | ||||
| chr4:112636879-112637181 | Rare:82 | ||||
| chr4:112637380-112637570 | Common:3; Rare:53 | ||||
| chr4:112817971-112818257 | Rare:45 | ||||
| chr4:113049466-113049802 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:113373087-113373341 | Common:1; Rare:76; Clinvar:8; Clinvar (benign):8 | ||||
| chr4:113761155-113761237 | Common:1; Rare:21 | ||||
| chr4:117085505-117085606 | Common:1; Rare:29 | ||||
| chr4:118685314-118685552 | Common:2; Rare:67 | ||||
| chr4:119212513-119212720 | Common:2; Rare:55 | ||||
| chr4:119628773-119629079 | Common:8; Rare:127 | ||||
| chr4:120066754-120066960 | Common:3; Rare:62 | ||||
| chr4:121801233-121801396 | Common:2; Rare:54 |