| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:27793256-27793486 | Common:4; Rare:52 | ||||
| chr19:27793657-27794074 | Common:1; Rare:103 | ||||
| chr19:33206587-33206619 | Rare:8 | ||||
| chr19:33391304-33391640 | Common:2; Rare:110; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:35904229-35904513 | Common:3; Rare:66; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:36142725-36142966 | Rare:58 | ||||
| chr19:36797273-36797562 | Common:1; Rare:64 | ||||
| chr19:38648865-38649126 | Common:1; Rare:42 | ||||
| chr19:38710086-38710326 | Common:1; Rare:68; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr19:39839756-39839915 | Common:1; Rare:31 | ||||
| chr19:39974347-39974564 | Common:2; Rare:64 | ||||
| chr19:40608312-40608593 | Common:2; Rare:102; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:40810781-40810840 | Rare:13 | ||||
| chr19:41176157-41176420 | Common:3; Rare:53 | ||||
| chr19:41352870-41353217 | Common:5; Rare:93; Clinvar (benign):2 |