| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:188153079-188153210 | Rare:26 | ||||
| chr3:188153649-188154230 | Common:1; Rare:138 | ||||
| chr3:190120362-190120544 | Rare:77; Clinvar (pathogenic):1 | ||||
| chr3:192917817-192917941 | Rare:60 | ||||
| chr3:193240992-193241318 | Common:3; Rare:112 | ||||
| chr3:193593081-193593404 | Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194135910-194136165 | Rare:62 | ||||
| chr3:194486963-194487168 | Common:4; Rare:100 | ||||
| chr3:195542910-195542957 | Rare:20 | ||||
| chr3:195543248-195543439 | Common:3; Rare:76 | ||||
| chr3:196082072-196082277 | Common:4; Rare:79 | ||||
| chr3:196318184-196318364 | Common:1; Rare:72 | ||||
| chr3:196503648-196504045 | Common:7; Rare:129 | ||||
| chr3:196568512-196568673 | Common:3; Rare:44 | ||||
| chr3:196867758-196867946 | Rare:65 |