| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:99638802-99638848 | Rare:9 | ||||
| chr3:99817562-99817924 | Rare:105 | ||||
| chr3:99876116-99876368 | Common:1; Rare:69 | ||||
| chr3:100260724-100261056 | Rare:96 | ||||
| chr3:100334583-100334786 | Common:2; Rare:72 | ||||
| chr3:100401398-100401580 | Common:1; Rare:34 | ||||
| chr3:100709428-100709721 | Common:5; Rare:77; Clinvar (benign):1 | ||||
| chr3:101561777-101561964 | Common:2; Rare:66 | ||||
| chr3:101574027-101574279 | Common:1; Rare:88 | ||||
| chr3:101677070-101677382 | Rare:105 | ||||
| chr3:101685816-101686085 | Common:4; Rare:67 | ||||
| chr3:101686480-101686860 | Common:2; Rare:155 | ||||
| chr3:101724545-101724650 | Rare:38 | ||||
| chr3:101779092-101779253 | Common:3; Rare:51 | ||||
| chr3:105868799-105869193 | Common:7; Rare:135 |