| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39182202-39182554 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39366315-39366457 | Rare:44 | ||||
| chr4:39406827-39407241 | Common:2; Rare:119 | ||||
| chr4:39458843-39459126 | Common:3; Rare:159; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527337-39527755 | Common:4; Rare:104 | ||||
| chr4:39527951-39528046 | Rare:25 | ||||
| chr4:39528091-39528224 | Common:1; Rare:30 | ||||
| chr4:39638841-39639209 | Common:1; Rare:141 | ||||
| chr4:39697936-39698229 | Common:2; Rare:125 | ||||
| chr4:40056673-40056944 | Common:4; Rare:92 | ||||
| chr4:40057197-40057280 | Common:1; Rare:24 | ||||
| chr4:40629728-40629932 | Common:1; Rare:54 | ||||
| chr4:40630130-40630225 | Common:1; Rare:14 | ||||
| chr4:41256706-41256981 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:41934660-41934754 | Common:1; Rare:14 |