| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49580535-49580682 | Rare:46 | ||||
| chr19:49640096-49640539 | Common:1; Rare:134 | ||||
| chr19:49665564-49666017 | Common:6; Rare:206; Clinvar (pathogenic):1 | ||||
| chr19:49817456-49817632 | Common:2; Rare:49 | ||||
| chr19:49818062-49818326 | Common:3; Rare:80; Clinvar:1 | ||||
| chr19:49851064-49851159 | Rare:37 | ||||
| chr19:49867205-49867251 | Rare:27; Clinvar (benign):5 | ||||
| chr19:49867518-49867643 | Common:2; Rare:41; Clinvar:1 | ||||
| chr19:49877309-49877726 | Common:1; Rare:109 | ||||
| chr19:49929096-49929210 | Common:3; Rare:35 | ||||
| chr19:49929408-49929567 | Common:4; Rare:58 | ||||
| chr19:50384089-50384377 | Common:2; Rare:122; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:50415583-50415815 | Common:1; Rare:79; Clinvar:16; Clinvar (benign):21 | ||||
| chr19:50418778-50418989 | Rare:74 | ||||
| chr19:50476208-50476560 | Common:1; Rare:164 |