| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39051945-39052094 | Common:1; Rare:56 | ||||
| chr3:39107497-39107741 | Common:4; Rare:81 | ||||
| chr3:39383258-39383437 | Common:2; Rare:32; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383530-39383662 | Rare:27; Clinvar:2 | ||||
| chr3:39406507-39406832 | Common:6; Rare:132 | ||||
| chr3:40309506-40309923 | Common:8; Rare:145 | ||||
| chr3:40457190-40457397 | Common:3; Rare:102 | ||||
| chr3:40477091-40477169 | Common:1; Rare:22 | ||||
| chr3:40505853-40506149 | Rare:73 | ||||
| chr3:40524823-40525019 | Common:1; Rare:55 | ||||
| chr3:41962032-41962312 | Common:4; Rare:67 | ||||
| chr3:42581848-42582141 | Common:4; Rare:92 | ||||
| chr3:42590630-42590961 | Common:3; Rare:102 | ||||
| chr3:42600372-42600772 | Common:2; Rare:152 | ||||
| chr3:42600854-42600928 | Rare:22 |