| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100400648-100400828 | Common:2; Rare:56 | ||||
| chr3:100401012-100401179 | Rare:47 | ||||
| chr3:100401307-100401594 | Common:1; Rare:65 | ||||
| chr3:100709228-100709752 | Common:6; Rare:158; Clinvar (benign):1 | ||||
| chr3:101513132-101513336 | Common:8; Rare:40 | ||||
| chr3:101561792-101562003 | Common:2; Rare:72 | ||||
| chr3:101574150-101574276 | Common:1; Rare:52 | ||||
| chr3:101589727-101589775 | Rare:10 | ||||
| chr3:101677079-101677271 | Rare:68 | ||||
| chr3:101686473-101686884 | Common:2; Rare:164 | ||||
| chr3:101724525-101724646 | Rare:41 | ||||
| chr3:101779172-101779728 | Common:6; Rare:148 | ||||
| chr3:101856171-101856346 | Rare:47 | ||||
| chr3:101857137-101857480 | Common:3; Rare:92 | ||||
| chr3:105366418-105366776 | Common:3; Rare:96 |