| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:186784134-186784477 | Common:1; Rare:138 | ||||
| chr3:186806449-186806541 | Rare:29 | ||||
| chr3:187291674-187291864 | Common:1; Rare:67 | ||||
| chr3:187737842-187738139 | Common:2; Rare:51 | ||||
| chr3:188152811-188153038 | Common:2; Rare:35 | ||||
| chr3:188153806-188154230 | Common:1; Rare:107 | ||||
| chr3:190322432-190322528 | Rare:28 | ||||
| chr3:190513903-190514114 | Common:2; Rare:61 | ||||
| chr3:192917836-192918003 | Common:2; Rare:76 | ||||
| chr3:193240998-193241329 | Common:4; Rare:109 | ||||
| chr3:193593096-193593402 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194487003-194487146 | Common:3; Rare:67 | ||||
| chr3:195543215-195543449 | Common:3; Rare:89 | ||||
| chr3:195885307-195885603 | Common:1; Rare:72 | ||||
| chr3:195892709-195892937 | Common:2; Rare:38 |