| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39383258-39383465 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383538-39383680 | Rare:32; Clinvar:2 | ||||
| chr3:39809328-39809669 | Common:3; Rare:114 | ||||
| chr3:40309432-40309814 | Common:9; Rare:127 | ||||
| chr3:40457201-40457388 | Common:3; Rare:91 | ||||
| chr3:40505948-40506159 | Rare:44 | ||||
| chr3:40524795-40525013 | Common:1; Rare:63 | ||||
| chr3:41962018-41962370 | Common:5; Rare:89 | ||||
| chr3:42581558-42581841 | Rare:66 | ||||
| chr3:42581900-42582137 | Common:3; Rare:73 | ||||
| chr3:42582255-42582453 | Common:1; Rare:48 | ||||
| chr3:42600328-42600750 | Common:3; Rare:168 | ||||
| chr3:42773206-42773278 | Common:1; Rare:26 | ||||
| chr3:42804272-42804677 | Common:2; Rare:113 | ||||
| chr3:42875797-42876210 | Rare:74 |