| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:99876096-99876278 | Common:1; Rare:50 | ||||
| chr3:100114434-100114975 | Common:3; Rare:110 | ||||
| chr3:100260704-100261037 | Rare:92 | ||||
| chr3:100334633-100334786 | Common:1; Rare:63 | ||||
| chr3:100401059-100401197 | Rare:40 | ||||
| chr3:100401378-100401582 | Common:1; Rare:45 | ||||
| chr3:100492410-100492668 | Common:2; Rare:88 | ||||
| chr3:100709200-100709721 | Common:9; Rare:157; Clinvar (benign):1 | ||||
| chr3:101513093-101513343 | Common:8; Rare:58 | ||||
| chr3:101561740-101561971 | Common:2; Rare:84 | ||||
| chr3:101574064-101574230 | Rare:56 | ||||
| chr3:101677054-101677171 | Rare:50 | ||||
| chr3:101686672-101686870 | Common:2; Rare:83 | ||||
| chr3:101724531-101724671 | Rare:51 | ||||
| chr3:101779127-101779281 | Common:4; Rare:52 |