| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:88149856-88150049 | Common:5; Rare:77 | ||||
| chr3:93979935-93980207 | Common:4; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94062861-94063104 | Rare:62 | ||||
| chr3:97764489-97764795 | Common:1; Rare:65; Clinvar (benign):1 | ||||
| chr3:98732442-98732500 | Rare:13 | ||||
| chr3:98900991-98901040 | Rare:9 | ||||
| chr3:98901594-98902014 | Common:1; Rare:159 | ||||
| chr3:99817543-99817924 | Rare:115 | ||||
| chr3:99876129-99876312 | Common:1; Rare:50 | ||||
| chr3:100260701-100261057 | Rare:104 | ||||
| chr3:100334650-100334786 | Common:1; Rare:58 | ||||
| chr3:100401398-100401576 | Common:1; Rare:33 | ||||
| chr3:100492413-100492651 | Common:2; Rare:81 | ||||
| chr3:100709224-100709559 | Common:6; Rare:116; Clinvar (benign):1 | ||||
| chr3:101513110-101513312 | Common:8; Rare:44 |