| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40580614-40580777 | Rare:57 | ||||
| chr19:40715056-40715174 | Rare:33 | ||||
| chr19:40750408-40750634 | Common:5; Rare:69 | ||||
| chr19:40751775-40751851 | Rare:19 | ||||
| chr19:40778033-40778360 | Common:1; Rare:103 | ||||
| chr19:41262268-41262566 | Rare:54 | ||||
| chr19:41309981-41310299 | Rare:114 | ||||
| chr19:41342206-41342320 | Rare:24; Clinvar (pathogenic):2 | ||||
| chr19:41353392-41353449 | Common:1; Rare:6 | ||||
| chr19:41353502-41353654 | Rare:25 | ||||
| chr19:41364100-41364228 | Common:1; Rare:45; Clinvar:1 | ||||
| chr19:41626999-41627233 | Common:2; Rare:50 | ||||
| chr19:41796434-41796660 | Rare:37 | ||||
| chr19:41860103-41860287 | Common:1; Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:41882995-41883264 | Common:1; Rare:53 |