| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37861711-37861948 | Common:1; Rare:50 | ||||
| chr3:38137075-38137449 | Common:1; Rare:82 | ||||
| chr3:39107532-39107708 | Common:3; Rare:55 | ||||
| chr3:39383568-39383668 | Rare:21; Clinvar:1 | ||||
| chr3:40309506-40309830 | Common:8; Rare:115 | ||||
| chr3:42013536-42013802 | Common:5; Rare:79 | ||||
| chr3:42581887-42582074 | Common:2; Rare:66 | ||||
| chr3:42582251-42582624 | Common:3; Rare:73 | ||||
| chr3:42600531-42600703 | Common:1; Rare:69 | ||||
| chr3:42804430-42804621 | Common:2; Rare:54 | ||||
| chr3:43690734-43690989 | Common:4; Rare:129; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44477633-44477804 | Common:1; Rare:34 | ||||
| chr3:44624891-44625087 | Common:2; Rare:60 | ||||
| chr3:44761600-44761794 | Common:3; Rare:67 | ||||
| chr3:44861803-44861918 | Common:2; Rare:54 |