| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:194487003-194487172 | Common:3; Rare:77 | ||||
| chr3:194672140-194672271 | Rare:66 | ||||
| chr3:195543215-195543494 | Common:3; Rare:108 | ||||
| chr3:196082080-196082247 | Common:2; Rare:67 | ||||
| chr3:196318184-196318340 | Common:1; Rare:65 | ||||
| chr3:196432395-196432550 | Common:1; Rare:68 | ||||
| chr3:196503569-196503956 | Common:8; Rare:131 | ||||
| chr3:196712228-196712344 | Common:2; Rare:37 | ||||
| chr3:196867770-196867946 | Rare:63 | ||||
| chr3:196942375-196942659 | Common:1; Rare:116 | ||||
| chr3:197298582-197298734 | Rare:47 | ||||
| chr3:197736784-197737183 | Common:3; Rare:129 | ||||
| chr3:197749742-197749962 | Common:1; Rare:81 | ||||
| chr3:197791196-197791274 | Rare:33 | ||||
| chr3:197949894-197950264 | Common:4; Rare:113; Clinvar (benign):2 |