| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:98522601-98522746 | Rare:33 | ||||
| chr3:98732376-98732543 | Rare:28 | ||||
| chr3:98732617-98732717 | Rare:22 | ||||
| chr3:99817539-99817900 | Common:1; Rare:107 | ||||
| chr3:99876129-99876257 | Rare:32 | ||||
| chr3:100260691-100261037 | Rare:94 | ||||
| chr3:100334526-100334793 | Common:2; Rare:85 | ||||
| chr3:100401398-100401582 | Common:1; Rare:34 | ||||
| chr3:100492420-100492927 | Common:11; Rare:124 | ||||
| chr3:100635358-100635784 | Common:2; Rare:104 | ||||
| chr3:100709235-100709730 | Common:6; Rare:150; Clinvar (benign):1 | ||||
| chr3:101513122-101513356 | Common:8; Rare:57 | ||||
| chr3:101561805-101561984 | Common:2; Rare:64 | ||||
| chr3:101574045-101574279 | Common:1; Rare:81 | ||||
| chr3:101677074-101677185 | Rare:47 |