| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:36993058-36993559 | Common:2; Rare:171; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:38137094-38137439 | Common:1; Rare:78 | ||||
| chr3:38138547-38138701 | Common:2; Rare:59; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:39051805-39052056 | Common:2; Rare:75 | ||||
| chr3:39107551-39107732 | Common:4; Rare:57 | ||||
| chr3:39383570-39383660 | Rare:18; Clinvar:1 | ||||
| chr3:39406446-39406763 | Common:7; Rare:129 | ||||
| chr3:40309469-40309853 | Common:9; Rare:130 | ||||
| chr3:40457201-40457388 | Common:3; Rare:91 | ||||
| chr3:41962027-41962240 | Common:3; Rare:52 | ||||
| chr3:42013529-42013819 | Common:5; Rare:87 | ||||
| chr3:42581909-42582140 | Common:3; Rare:70 | ||||
| chr3:42600328-42600743 | Common:3; Rare:166 | ||||
| chr3:42773214-42773357 | Common:1; Rare:38 | ||||
| chr3:42804422-42804657 | Common:2; Rare:68 |