| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:190120427-190120476 | Rare:18; Clinvar (pathogenic):1 | ||||
| chr3:190120815-190120999 | Rare:54 | ||||
| chr3:190513902-190514114 | Common:2; Rare:61 | ||||
| chr3:191329308-191329707 | Common:3; Rare:119 | ||||
| chr3:192917811-192918016 | Common:2; Rare:93 | ||||
| chr3:193593105-193593376 | Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:195543127-195543475 | Common:4; Rare:117 | ||||
| chr3:195583988-195584405 | Common:12; Rare:90 | ||||
| chr3:195895928-195896002 | Rare:26 | ||||
| chr3:196082034-196082261 | Common:2; Rare:93 | ||||
| chr3:196318184-196318374 | Common:1; Rare:76 | ||||
| chr3:196503630-196504045 | Common:8; Rare:133 | ||||
| chr3:196568518-196568641 | Common:1; Rare:31 | ||||
| chr3:196712195-196712348 | Common:2; Rare:52 | ||||
| chr3:196867748-196867953 | Rare:71 |