| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38165766-38165822 | Rare:17 | ||||
| chr3:39051944-39052035 | Common:1; Rare:34 | ||||
| chr3:39107555-39107658 | Common:1; Rare:38 | ||||
| chr3:39153485-39153783 | Common:4; Rare:104 | ||||
| chr3:39383283-39383694 | Common:3; Rare:90; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:39406580-39406761 | Common:2; Rare:78 | ||||
| chr3:40309448-40309819 | Common:9; Rare:127 | ||||
| chr3:40387052-40387198 | Common:1; Rare:48 | ||||
| chr3:40457204-40457463 | Common:6; Rare:120 | ||||
| chr3:40457566-40457990 | Common:4; Rare:127 | ||||
| chr3:40524815-40525023 | Common:1; Rare:60 | ||||
| chr3:41238880-41239174 | Rare:87 | ||||
| chr3:41962045-41962562 | Common:6; Rare:125 | ||||
| chr3:42013541-42013792 | Common:5; Rare:75 | ||||
| chr3:42581900-42582137 | Common:3; Rare:73 |