| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:80770346-80770603 | Common:3; Rare:38 | ||||
| chr3:101676254-101676513 | Common:2; Rare:89 | ||||
| chr3:107240594-107240759 | Rare:69 | ||||
| chr3:111802378-111802610 | Common:1; Rare:26 | ||||
| chr3:125916358-125916624 | Common:4; Rare:80 | ||||
| chr3:130112400-130112547 | Common:2; Rare:37 | ||||
| chr3:150408855-150408992 | Rare:39 | ||||
| chr3:152113502-152113703 | Common:1; Rare:41 | ||||
| chr3:157174840-157175257 | Common:3; Rare:180 | ||||
| chr3:160515233-160515489 | Common:1; Rare:49 | ||||
| chr3:169765048-169765195 | Rare:69; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:174775710-174775939 | Common:1; Rare:41 | ||||
| chr3:191425425-191425528 | Rare:21 | ||||
| chr3:194583866-194584020 | Common:10; Rare:56 | ||||
| chr3:195657926-195658120 | Common:11; Rare:34 |