| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:94062856-94063033 | Rare:52 | ||||
| chr3:97764439-97764793 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr3:97972390-97972500 | Common:3; Rare:41 | ||||
| chr3:98522858-98523130 | Common:1; Rare:81 | ||||
| chr3:99817543-99817920 | Rare:113 | ||||
| chr3:100260724-100261021 | Rare:77 | ||||
| chr3:100334650-100334783 | Common:1; Rare:57 | ||||
| chr3:100401389-100401602 | Common:1; Rare:42 | ||||
| chr3:100709226-100709411 | Common:2; Rare:68 | ||||
| chr3:101513118-101513324 | Common:8; Rare:41 | ||||
| chr3:101561743-101561927 | Common:2; Rare:64 | ||||
| chr3:101573983-101574218 | Rare:81 | ||||
| chr3:101677052-101677297 | Rare:87 | ||||
| chr3:101686672-101686880 | Common:2; Rare:86 | ||||
| chr3:101724508-101724642 | Rare:43 |