| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:190322126-190322541 | Common:3; Rare:117; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:191329292-191329667 | Common:3; Rare:115 | ||||
| chr3:192917814-192918023 | Common:2; Rare:92 | ||||
| chr3:193593075-193593380 | Rare:99; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194486228-194486353 | Common:5; Rare:28 | ||||
| chr3:194486951-194487177 | Common:4; Rare:113 | ||||
| chr3:194672150-194672271 | Rare:60 | ||||
| chr3:195543142-195543493 | Common:4; Rare:121 | ||||
| chr3:195583878-195584405 | Common:12; Rare:107 | ||||
| chr3:196082040-196082259 | Common:2; Rare:90 | ||||
| chr3:196287616-196287831 | Common:1; Rare:67 | ||||
| chr3:196317836-196317992 | Common:1; Rare:41 | ||||
| chr3:196318184-196318354 | Common:1; Rare:70 | ||||
| chr3:196338368-196338645 | Rare:69 | ||||
| chr3:196432395-196432604 | Common:1; Rare:86 |