| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10101964-10102364 | Common:2; Rare:73 | ||||
| chr19:10102718-10103131 | Common:3; Rare:214 | ||||
| chr19:10106132-10106425 | Common:5; Rare:189 | ||||
| chr19:10106508-10106635 | Common:1; Rare:54 | ||||
| chr19:10107368-10107815 | Common:5; Rare:288 | ||||
| chr19:10116908-10117174 | Common:1; Rare:80 | ||||
| chr19:10118913-10120149 | Common:12; Rare:1138 | ||||
| chr19:10166262-10166951 | Common:2; Rare:239; Clinvar:8; Clinvar (benign):4 | ||||
| chr19:10194049-10194449 | Common:1; Rare:92 | ||||
| chr19:10194514-10195313 | Common:13; Rare:1119; Clinvar:3; Clinvar (benign):16 | ||||
| chr19:10230380-10231110 | Common:11; Rare:321 | ||||
| chr19:10231252-10231657 | Common:6; Rare:216 | ||||
| chr19:10251710-10252042 | Common:6; Rare:328 | ||||
| chr19:10252050-10252689 | Common:11; Rare:580 | ||||
| chr19:10269653-10270579 | Common:3; Rare:347 |