| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41219073-41219283 | Rare:41 | ||||
| chr19:41353786-41354100 | Common:2; Rare:102 | ||||
| chr19:41363800-41363992 | Common:1; Rare:66; Clinvar:1 | ||||
| chr19:43527182-43527310 | Common:4; Rare:49; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr19:44141472-44141588 | Common:1; Rare:15 | ||||
| chr19:45038943-45039097 | Rare:53 | ||||
| chr19:45405013-45405223 | Common:1; Rare:45 | ||||
| chr19:45406339-45406649 | Common:1; Rare:68 | ||||
| chr19:45423829-45424088 | Common:3; Rare:57 | ||||
| chr19:45450733-45451013 | Common:4; Rare:52 | ||||
| chr19:45507228-45507525 | Common:1; Rare:80 | ||||
| chr19:45692374-45692691 | Common:1; Rare:72 | ||||
| chr19:46296792-46297062 | Common:4; Rare:104 | ||||
| chr19:46601021-46601409 | Common:4; Rare:123; Clinvar (benign):1 | ||||
| chr19:47256300-47256568 | Rare:76 |