| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:99817548-99817956 | Rare:231 | ||||
| chr3:99876114-99876351 | Common:2; Rare:116 | ||||
| chr3:100260666-100261045 | Rare:108 | ||||
| chr3:100334624-100334786 | Common:2; Rare:130 | ||||
| chr3:100400984-100401257 | Rare:129 | ||||
| chr3:100401352-100401608 | Common:2; Rare:107 | ||||
| chr3:100492292-100492715 | Common:4; Rare:205 | ||||
| chr3:100709218-100709688 | Common:15; Rare:277; Clinvar (benign):2 | ||||
| chr3:101513113-101513353 | Common:16; Rare:96 | ||||
| chr3:101561743-101561964 | Common:4; Rare:149 | ||||
| chr3:101574049-101574257 | Common:1; Rare:138 | ||||
| chr3:101574480-101575040 | Common:4; Rare:213 | ||||
| chr3:101677068-101677184 | Rare:90 | ||||
| chr3:101686642-101686890 | Common:4; Rare:188 | ||||
| chr3:101724510-101724667 | Rare:82 |