| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100401383-100401580 | Common:1; Rare:42 | ||||
| chr3:100492105-100492346 | Rare:52 | ||||
| chr3:100492420-100492866 | Common:11; Rare:113 | ||||
| chr3:100635355-100635716 | Common:2; Rare:82 | ||||
| chr3:100709214-100709748 | Common:9; Rare:159; Clinvar (benign):1 | ||||
| chr3:101513122-101513324 | Common:8; Rare:41 | ||||
| chr3:101561789-101561992 | Common:2; Rare:70 | ||||
| chr3:101574003-101574230 | Rare:79 | ||||
| chr3:101677079-101677164 | Rare:38 | ||||
| chr3:101685816-101686032 | Common:3; Rare:58 | ||||
| chr3:101686489-101686910 | Common:2; Rare:166 | ||||
| chr3:101724554-101724654 | Rare:38 | ||||
| chr3:105366629-105366946 | Common:2; Rare:89 | ||||
| chr3:105367167-105367291 | Common:1; Rare:29 | ||||
| chr3:105868799-105869193 | Common:7; Rare:135 |