| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:88058933-88059308 | Common:3; Rare:140 | ||||
| chr3:88149657-88149758 | Rare:21 | ||||
| chr3:88149862-88150018 | Rare:53 | ||||
| chr3:94028503-94028671 | Rare:23 | ||||
| chr3:94062877-94063101 | Rare:57 | ||||
| chr3:97764499-97764802 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:98593110-98593171 | Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:99638462-99638612 | Common:1; Rare:34 | ||||
| chr3:99817568-99817904 | Rare:97 | ||||
| chr3:99850941-99851281 | Common:1; Rare:77 | ||||
| chr3:99876156-99876335 | Common:1; Rare:49 | ||||
| chr3:100260640-100261028 | Rare:98 | ||||
| chr3:100334638-100334773 | Common:1; Rare:57 | ||||
| chr3:101513129-101513319 | Common:8; Rare:39 | ||||
| chr3:101574032-101574234 | Rare:68 |