| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:93973800-93974030 | Rare:60; Clinvar:5 | ||||
| chr3:94062910-94063083 | Rare:40 | ||||
| chr3:97764448-97764569 | Rare:27 | ||||
| chr3:97764696-97764795 | Common:1; Rare:21; Clinvar (benign):1 | ||||
| chr3:97821892-97822179 | Common:2; Rare:97 | ||||
| chr3:97972380-97972497 | Common:3; Rare:48 | ||||
| chr3:98522589-98522755 | Rare:37 | ||||
| chr3:98732417-98732512 | Rare:18 | ||||
| chr3:98732575-98732723 | Rare:29 | ||||
| chr3:98901641-98901973 | Common:1; Rare:124 | ||||
| chr3:99638280-99638669 | Common:1; Rare:85 | ||||
| chr3:99817467-99817972 | Common:1; Rare:155 | ||||
| chr3:99876079-99876257 | Common:1; Rare:51 | ||||
| chr3:100260724-100261028 | Rare:78 | ||||
| chr3:100261336-100261617 | Common:1; Rare:58 |