| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:101330525-101330602 | Rare:20 | ||||
| chr2:101486431-101486780 | Common:1; Rare:61 | ||||
| chr2:101699082-101699408 | Rare:64 | ||||
| chr2:101702638-101702857 | Rare:43 | ||||
| chr2:101747501-101747532 | Rare:5 | ||||
| chr2:101766566-101766617 | Rare:7 | ||||
| chr2:101766939-101767135 | Common:1; Rare:38 | ||||
| chr2:101775060-101775172 | Common:2; Rare:22 | ||||
| chr2:101790680-101790777 | Rare:22; Clinvar (benign):1 | ||||
| chr2:101795755-101795932 | Common:2; Rare:36 | ||||
| chr2:101798001-101798075 | Rare:15 | ||||
| chr2:101831625-101832103 | Common:1; Rare:89 | ||||
| chr2:101834379-101834677 | Common:1; Rare:46 | ||||
| chr2:101842548-101842988 | Common:1; Rare:76 | ||||
| chr2:101844510-101844692 | Rare:30 |