| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39153485-39153737 | Common:3; Rare:84 | ||||
| chr3:39383258-39383437 | Common:2; Rare:32; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383538-39383660 | Rare:26; Clinvar:2 | ||||
| chr3:39406574-39406759 | Common:2; Rare:79 | ||||
| chr3:40309460-40309826 | Common:9; Rare:125 | ||||
| chr3:40457196-40457410 | Common:3; Rare:104 | ||||
| chr3:40524815-40525013 | Common:1; Rare:58 | ||||
| chr3:41962032-41962626 | Common:8; Rare:150 | ||||
| chr3:42581903-42582137 | Common:3; Rare:72 | ||||
| chr3:42600320-42600709 | Common:3; Rare:153 | ||||
| chr3:42600862-42601000 | Rare:51 | ||||
| chr3:42804427-42804693 | Common:2; Rare:87 | ||||
| chr3:42809296-42809490 | Rare:34 | ||||
| chr3:43690634-43690950 | Common:4; Rare:117; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44338079-44338180 | Common:2; Rare:37 |