| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40309491-40309808 | Common:9; Rare:109 | ||||
| chr3:40457231-40457406 | Common:2; Rare:89 | ||||
| chr3:40524815-40524916 | Common:1; Rare:26 | ||||
| chr3:41962040-41962357 | Common:4; Rare:76 | ||||
| chr3:42581907-42582137 | Common:3; Rare:72 | ||||
| chr3:42600355-42600709 | Common:3; Rare:142 | ||||
| chr3:42773206-42773345 | Common:1; Rare:42 | ||||
| chr3:42804443-42804657 | Common:2; Rare:63 | ||||
| chr3:42936326-42936446 | Common:1; Rare:33 | ||||
| chr3:43621919-43622322 | Common:2; Rare:118; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:44338057-44338190 | Common:2; Rare:46 | ||||
| chr3:44338680-44338798 | Common:3; Rare:45 | ||||
| chr3:44477641-44477695 | Rare:14 | ||||
| chr3:44624851-44625063 | Common:2; Rare:59 | ||||
| chr3:44729516-44729678 | Common:1; Rare:61 |