| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40798680-40799210 | Common:9; Rare:328 | ||||
| chr19:41218470-41218987 | Common:17; Rare:168 | ||||
| chr19:41226060-41226770 | Common:5; Rare:274 | ||||
| chr19:41262409-41262617 | Rare:33 | ||||
| chr19:41263690-41264224 | Rare:210 | ||||
| chr19:41264880-41265160 | Common:4; Rare:102 | ||||
| chr19:41310139-41310540 | Common:1; Rare:268 | ||||
| chr19:41353330-41353543 | Common:2; Rare:57 | ||||
| chr19:41353834-41354176 | Common:2; Rare:193 | ||||
| chr19:41363791-41364005 | Common:2; Rare:141; Clinvar:2 | ||||
| chr19:41364060-41364430 | Common:2; Rare:207; Clinvar:6 | ||||
| chr19:41397548-41397872 | Common:15; Rare:212; Clinvar (benign):11 | ||||
| chr19:41439240-41439790 | Common:7; Rare:239 | ||||
| chr19:41859560-41859930 | Common:2; Rare:214 | ||||
| chr19:41860052-41860329 | Common:4; Rare:188; Clinvar:8; Clinvar (benign):4 |