| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40309479-40309851 | Common:9; Rare:126 | ||||
| chr3:40457204-40457379 | Common:3; Rare:86 | ||||
| chr3:41962059-41962363 | Common:4; Rare:70 | ||||
| chr3:42581913-42582137 | Common:3; Rare:69 | ||||
| chr3:42600365-42600709 | Common:2; Rare:136 | ||||
| chr3:42804436-42804608 | Common:2; Rare:50 | ||||
| chr3:43690817-43690953 | Common:1; Rare:61; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44477631-44477807 | Common:1; Rare:37 | ||||
| chr3:44761590-44761813 | Common:3; Rare:80 | ||||
| chr3:44861781-44861918 | Common:2; Rare:61 | ||||
| chr3:44976138-44976272 | Common:2; Rare:53 | ||||
| chr3:45689155-45689459 | Common:2; Rare:104 | ||||
| chr3:45995814-45995848 | Rare:11; Clinvar:1 | ||||
| chr3:47380806-47381062 | Rare:79 | ||||
| chr3:47802851-47803195 | Common:1; Rare:109 |