| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:98770216-98770917 | Common:4; Rare:127 | ||||
| chr3:98771094-98771149 | Rare:13 | ||||
| chr3:98771982-98772312 | Common:2; Rare:63 | ||||
| chr3:98772315-98772383 | Common:1; Rare:6 | ||||
| chr3:98901638-98902014 | Common:1; Rare:144 | ||||
| chr3:99817548-99817934 | Rare:118 | ||||
| chr3:100260685-100261021 | Rare:90 | ||||
| chr3:100334650-100334794 | Common:1; Rare:62 | ||||
| chr3:100401359-100401592 | Common:1; Rare:54 | ||||
| chr3:100492402-100492817 | Common:11; Rare:120 | ||||
| chr3:100709214-100709726 | Common:9; Rare:155; Clinvar (benign):1 | ||||
| chr3:101513110-101513352 | Common:8; Rare:58 | ||||
| chr3:101561746-101561971 | Common:2; Rare:84 | ||||
| chr3:101574036-101574276 | Common:1; Rare:83 | ||||
| chr3:101677052-101677171 | Rare:50 |