| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41439521-41439686 | Common:1; Rare:44 | ||||
| chr19:41860041-41860285 | Common:1; Rare:91; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:41959272-41959466 | Common:1; Rare:63 | ||||
| chr19:41994069-41994195 | Rare:32; Clinvar (benign):1 | ||||
| chr19:41994197-41994450 | Common:1; Rare:60; Clinvar:2 | ||||
| chr19:42070138-42070473 | Rare:80 | ||||
| chr19:42075805-42076199 | Rare:112 | ||||
| chr19:42220120-42220354 | Common:2; Rare:64 | ||||
| chr19:42268224-42268561 | Rare:68 | ||||
| chr19:42301995-42302140 | Rare:37 | ||||
| chr19:42302301-42302818 | Common:1; Rare:133 | ||||
| chr19:42325380-42325687 | Rare:81 | ||||
| chr19:43527144-43527292 | Common:5; Rare:62; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43575459-43575852 | Common:2; Rare:102 | ||||
| chr19:43580295-43580643 | Common:4; Rare:55 |