| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:88149654-88149761 | Rare:23 | ||||
| chr3:88149856-88150055 | Common:5; Rare:79 | ||||
| chr3:94062887-94063097 | Rare:52 | ||||
| chr3:97764478-97764802 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:98522586-98522715 | Rare:34 | ||||
| chr3:98593645-98593860 | Common:2; Rare:74 | ||||
| chr3:98732427-98732512 | Rare:15 | ||||
| chr3:98732610-98732742 | Rare:25 | ||||
| chr3:98732920-98733266 | Common:2; Rare:88 | ||||
| chr3:99817562-99817924 | Rare:105 | ||||
| chr3:99876107-99876185 | Rare:20 | ||||
| chr3:99876193-99876347 | Common:1; Rare:43 | ||||
| chr3:100260749-100261057 | Rare:88 | ||||
| chr3:100334550-100334794 | Common:2; Rare:83 | ||||
| chr3:100401052-100401192 | Rare:43 |