| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:88149605-88149727 | Common:1; Rare:27 | ||||
| chr3:88149856-88150079 | Common:5; Rare:87 | ||||
| chr3:94062972-94063095 | Rare:21 | ||||
| chr3:97764496-97764802 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:98732427-98732532 | Rare:17 | ||||
| chr3:98732619-98732812 | Rare:42 | ||||
| chr3:99638538-99638624 | Rare:16 | ||||
| chr3:99817568-99817900 | Rare:95 | ||||
| chr3:99876107-99876257 | Rare:38 | ||||
| chr3:100114433-100114948 | Common:3; Rare:99 | ||||
| chr3:100260701-100261037 | Rare:92 | ||||
| chr3:100401402-100401580 | Common:1; Rare:33 | ||||
| chr3:100492413-100492658 | Common:2; Rare:83 | ||||
| chr3:101561746-101561915 | Common:1; Rare:60 | ||||
| chr3:101573983-101574279 | Common:1; Rare:105 |