| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100260699-100261074 | Rare:114 | ||||
| chr3:100334655-100334813 | Common:1; Rare:69 | ||||
| chr3:100400960-100401223 | Common:1; Rare:72 | ||||
| chr3:100401343-100401594 | Common:1; Rare:59 | ||||
| chr3:100401994-100402032 | Common:1; Rare:7 | ||||
| chr3:100492445-100492785 | Common:11; Rare:99 | ||||
| chr3:100709228-100709602 | Common:5; Rare:125; Clinvar (benign):1 | ||||
| chr3:101513109-101513208 | Rare:30 | ||||
| chr3:101561732-101561980 | Common:2; Rare:90 | ||||
| chr3:101573977-101574279 | Common:1; Rare:108 | ||||
| chr3:101677096-101677290 | Rare:69 | ||||
| chr3:101686425-101686884 | Common:2; Rare:187 | ||||
| chr3:101724484-101724663 | Rare:59 | ||||
| chr3:101779124-101779328 | Common:5; Rare:66 | ||||
| chr3:105366427-105366944 | Common:4; Rare:140 |