| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:191375918-191376224 | Common:3; Rare:55 | ||||
| chr3:191376700-191377004 | Common:1; Rare:62 | ||||
| chr3:191380687-191380888 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:193830724-193830872 | Common:1; Rare:27 | ||||
| chr3:193831765-193831806 | Rare:6 | ||||
| chr3:193837432-193837483 | Common:2; Rare:9 | ||||
| chr3:193837493-193837571 | Rare:14 | ||||
| chr3:194091238-194091541 | Common:1; Rare:49 | ||||
| chr3:194135077-194135223 | Rare:47 | ||||
| chr3:194322797-194323154 | Common:5; Rare:77 | ||||
| chr3:194323975-194324033 | Common:1; Rare:7 | ||||
| chr3:194410091-194410287 | Rare:31 | ||||
| chr3:194583814-194584021 | Common:10; Rare:75 | ||||
| chr3:194685856-194685924 | Common:1; Rare:24 | ||||
| chr3:194688449-194688684 | Common:1; Rare:61 |