| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:97821902-97822088 | Rare:69 | ||||
| chr3:98732385-98732536 | Rare:26 | ||||
| chr3:98732619-98732698 | Rare:15 | ||||
| chr3:98732707-98732863 | Rare:33 | ||||
| chr3:99638451-99638616 | Common:1; Rare:39 | ||||
| chr3:99817562-99817924 | Rare:105 | ||||
| chr3:99876102-99876287 | Common:1; Rare:49 | ||||
| chr3:100260724-100261061 | Rare:99 | ||||
| chr3:100334639-100334780 | Common:1; Rare:59 | ||||
| chr3:100401407-100401580 | Common:1; Rare:30 | ||||
| chr3:100492413-100492658 | Common:2; Rare:83 | ||||
| chr3:100709077-100709639 | Common:10; Rare:164; Clinvar (benign):1 | ||||
| chr3:101513129-101513312 | Common:8; Rare:38 | ||||
| chr3:101561759-101561961 | Common:2; Rare:78 | ||||
| chr3:101573973-101574225 | Rare:89 |