| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:93979813-93980190 | Common:3; Rare:118; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:94028652-94028954 | Rare:49 | ||||
| chr3:94062904-94063069 | Rare:42 | ||||
| chr3:97764706-97764796 | Common:1; Rare:18; Clinvar (benign):1 | ||||
| chr3:97821943-97822175 | Common:2; Rare:78 | ||||
| chr3:99817556-99817925 | Rare:110 | ||||
| chr3:99876096-99876254 | Rare:44 | ||||
| chr3:100260715-100261021 | Rare:81 | ||||
| chr3:100334650-100334769 | Common:1; Rare:49 | ||||
| chr3:100401402-100401576 | Common:1; Rare:32 | ||||
| chr3:100492445-100492668 | Common:2; Rare:73 | ||||
| chr3:100709203-100709698 | Common:9; Rare:150; Clinvar (benign):1 | ||||
| chr3:101561777-101561910 | Common:1; Rare:42 | ||||
| chr3:101573936-101574371 | Common:2; Rare:144 | ||||
| chr3:101677097-101677171 | Rare:33 |