| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:88149856-88150049 | Common:5; Rare:77 | ||||
| chr3:94062910-94063083 | Rare:40 | ||||
| chr3:97764485-97764802 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821921-97822226 | Common:2; Rare:104 | ||||
| chr3:98522601-98522662 | Rare:13 | ||||
| chr3:98522847-98523066 | Common:1; Rare:73 | ||||
| chr3:98732422-98732512 | Rare:17 | ||||
| chr3:98732678-98732733 | Rare:12 | ||||
| chr3:99638328-99638642 | Common:1; Rare:68 | ||||
| chr3:99638802-99638998 | Common:1; Rare:33 | ||||
| chr3:99817568-99817956 | Rare:121 | ||||
| chr3:99876072-99876320 | Common:2; Rare:72 | ||||
| chr3:100260704-100261057 | Rare:104 | ||||
| chr3:100334650-100334786 | Common:1; Rare:58 | ||||
| chr3:100401407-100401582 | Common:1; Rare:30 |