| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:99817568-99817934 | Rare:111 | ||||
| chr3:99850941-99851193 | Rare:65 | ||||
| chr3:99876124-99876269 | Common:1; Rare:38 | ||||
| chr3:100260733-100261028 | Rare:75 | ||||
| chr3:100334526-100334782 | Common:2; Rare:81 | ||||
| chr3:100492404-100492792 | Common:11; Rare:116 | ||||
| chr3:100709235-100709698 | Common:6; Rare:141; Clinvar (benign):1 | ||||
| chr3:101573995-101574237 | Rare:83 | ||||
| chr3:101677074-101677171 | Rare:43 | ||||
| chr3:101685820-101686192 | Common:4; Rare:92 | ||||
| chr3:101686666-101686870 | Common:2; Rare:84 | ||||
| chr3:101724342-101724650 | Common:1; Rare:69 | ||||
| chr3:101779092-101779253 | Common:3; Rare:51 | ||||
| chr3:105366534-105366777 | Common:3; Rare:71 | ||||
| chr3:105868784-105869193 | Common:7; Rare:136 |