| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42302270-42302642 | Rare:110 | ||||
| chr19:42313216-42313353 | Common:1; Rare:31 | ||||
| chr19:42325200-42325717 | Rare:128 | ||||
| chr19:42423515-42423767 | Common:4; Rare:92 | ||||
| chr19:42423927-42424077 | Rare:28 | ||||
| chr19:43463734-43463943 | Rare:73 | ||||
| chr19:43503914-43503974 | Rare:25 | ||||
| chr19:43504064-43504301 | Common:5; Rare:84 | ||||
| chr19:43504533-43504555 | Rare:1 | ||||
| chr19:43504699-43504752 | Rare:5 | ||||
| chr19:43527158-43527344 | Common:5; Rare:69; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43527458-43527566 | Rare:22 | ||||
| chr19:43533084-43533450 | Common:2; Rare:109 | ||||
| chr19:43533791-43534241 | Common:2; Rare:99 | ||||
| chr19:43575449-43575928 | Common:3; Rare:119 |