| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:88058914-88059304 | Common:3; Rare:147 | ||||
| chr3:88149856-88150064 | Common:5; Rare:83 | ||||
| chr3:89107537-89107749 | Common:2; Rare:62 | ||||
| chr3:93979912-93980190 | Common:3; Rare:99; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:94062910-94063091 | Rare:41 | ||||
| chr3:96814422-96814595 | Rare:63 | ||||
| chr3:97764472-97764594 | Rare:22 | ||||
| chr3:97764706-97764802 | Common:1; Rare:19; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821856-97822088 | Rare:86 | ||||
| chr3:97972380-97972485 | Common:3; Rare:41 | ||||
| chr3:98522851-98523098 | Common:1; Rare:75 | ||||
| chr3:98732239-98732501 | Rare:52 | ||||
| chr3:99817562-99817900 | Rare:96 | ||||
| chr3:99876107-99876276 | Common:1; Rare:43 | ||||
| chr3:100260704-100261061 | Rare:107 |