| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184135209-184135385 | Common:2; Rare:50; Clinvar:5 | ||||
| chr3:184711953-184712243 | Common:1; Rare:97 | ||||
| chr3:185282858-185283003 | Common:1; Rare:38 | ||||
| chr3:186783259-186783617 | Common:1; Rare:148 | ||||
| chr3:188153714-188153872 | Common:1; Rare:26 | ||||
| chr3:188154067-188154212 | Rare:38 | ||||
| chr3:190120382-190120585 | Rare:81; Clinvar (pathogenic):1 | ||||
| chr3:193593101-193593298 | Rare:60; Clinvar:1 | ||||
| chr3:196287737-196287831 | Common:1; Rare:25 | ||||
| chr3:196318191-196318318 | Common:1; Rare:55 | ||||
| chr3:196867785-196867931 | Rare:48 | ||||
| chr3:196942515-196942659 | Common:1; Rare:58 | ||||
| chr3:197749695-197749964 | Common:1; Rare:94 | ||||
| chr3:197949890-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197959986-197960259 | Common:1; Rare:95 |