| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:38664221-38664306 | Rare:29 | ||||
| chr4:38867643-38867833 | Common:1; Rare:69 | ||||
| chr4:39182349-39182554 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39366306-39366422 | Rare:34 | ||||
| chr4:39458856-39459126 | Common:3; Rare:154; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527400-39527775 | Common:2; Rare:99 | ||||
| chr4:39527952-39528085 | Common:1; Rare:32 | ||||
| chr4:39638829-39639170 | Common:1; Rare:124 | ||||
| chr4:39697981-39698192 | Common:1; Rare:83 | ||||
| chr4:40056666-40056941 | Common:4; Rare:92 | ||||
| chr4:40057197-40057273 | Common:1; Rare:24 | ||||
| chr4:40192860-40193015 | Common:1; Rare:25 | ||||
| chr4:40193393-40193673 | Rare:47 | ||||
| chr4:40196928-40197128 | Rare:35 | ||||
| chr4:40629756-40629932 | Common:1; Rare:50 |