| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37990569-37990800 | Common:1; Rare:43 | ||||
| chr3:38029605-38029844 | Common:1; Rare:47 | ||||
| chr3:38165700-38165868 | Rare:55 | ||||
| chr3:39051939-39052042 | Common:1; Rare:36 | ||||
| chr3:39107597-39107680 | Common:2; Rare:26 | ||||
| chr3:39383554-39383660 | Rare:26; Clinvar:2 | ||||
| chr3:39406600-39406758 | Common:2; Rare:69 | ||||
| chr3:40309491-40309803 | Common:9; Rare:108 | ||||
| chr3:40457201-40457405 | Common:3; Rare:101 | ||||
| chr3:40524812-40524911 | Common:1; Rare:26 | ||||
| chr3:41962045-41962568 | Common:6; Rare:127 | ||||
| chr3:42160071-42160222 | Common:1; Rare:33 | ||||
| chr3:42581900-42582137 | Common:3; Rare:73 | ||||
| chr3:42804427-42804669 | Common:2; Rare:75 | ||||
| chr3:43621914-43622192 | Common:2; Rare:93; Clinvar:7; Clinvar (benign):1 |