| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100322469-100322696 | Rare:26 | ||||
| chr3:100362469-100362626 | Common:1; Rare:30 | ||||
| chr3:100744790-100744960 | Common:3; Rare:49; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:101576471-101576748 | Common:3; Rare:60 | ||||
| chr3:101576879-101576920 | Rare:9 | ||||
| chr3:101576981-101577088 | Rare:31 | ||||
| chr3:101676178-101676503 | Common:5; Rare:102 | ||||
| chr3:105403996-105404179 | Rare:31 | ||||
| chr3:105404934-105405225 | Common:1; Rare:63 | ||||
| chr3:105446247-105446382 | Common:1; Rare:16 | ||||
| chr3:105526627-105526704 | Rare:8 | ||||
| chr3:105547144-105547521 | Common:2; Rare:90 | ||||
| chr3:105678125-105678380 | Rare:55 | ||||
| chr3:105837080-105837427 | Common:1; Rare:64 | ||||
| chr3:106850577-106850684 | Common:1; Rare:13 |