| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10333497-10333709 | Rare:70 | ||||
| chr19:10502702-10502919 | Rare:57 | ||||
| chr19:10503300-10503405 | Rare:25 | ||||
| chr19:10559656-10559922 | Common:4; Rare:109 | ||||
| chr19:10653818-10653970 | Common:1; Rare:55 | ||||
| chr19:10683503-10683642 | Common:2; Rare:63 | ||||
| chr19:10795941-10796321 | Rare:94; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:10798397-10798572 | Rare:54; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:10836268-10836551 | Common:2; Rare:72 | ||||
| chr19:10928517-10928802 | Common:2; Rare:79 | ||||
| chr19:10960689-10961141 | Common:3; Rare:168; Clinvar (benign):1 | ||||
| chr19:11089269-11089551 | Rare:55; Clinvar:12; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:11090356-11090600 | Common:2; Rare:72 | ||||
| chr19:11197483-11197691 | Common:1; Rare:64 | ||||
| chr19:11197796-11198138 | Common:2; Rare:95 |