| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:8501535-8501931 | Common:3; Rare:146 | ||||
| chr3:9362984-9363134 | Common:1; Rare:54 | ||||
| chr3:9397436-9397670 | Rare:78 | ||||
| chr3:9792396-9792570 | Rare:48 | ||||
| chr3:9792732-9793121 | Common:3; Rare:134 | ||||
| chr3:9843993-9844135 | Common:2; Rare:49 | ||||
| chr3:9890503-9890676 | Common:2; Rare:62 | ||||
| chr3:9933524-9933857 | Common:2; Rare:135; Clinvar:3 | ||||
| chr3:10026323-10026484 | Rare:48 | ||||
| chr3:10115520-10115807 | Common:3; Rare:89 | ||||
| chr3:11225904-11226014 | Rare:14 | ||||
| chr3:11272227-11272413 | Common:1; Rare:38 | ||||
| chr3:11846834-11846996 | Common:1; Rare:46 | ||||
| chr3:12664084-12664274 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:12841465-12841883 | Common:2; Rare:134 |