| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40465687-40466112 | Common:3; Rare:134 | ||||
| chr19:40609641-40609787 | Common:1; Rare:51; Clinvar (benign):2 | ||||
| chr19:40715076-40715171 | Rare:26 | ||||
| chr19:40716872-40717009 | Common:1; Rare:45 | ||||
| chr19:40750424-40750755 | Common:5; Rare:87 | ||||
| chr19:40751110-40751259 | Common:1; Rare:40 | ||||
| chr19:40777921-40778280 | Common:1; Rare:98 | ||||
| chr19:41218711-41219002 | Common:7; Rare:62 | ||||
| chr19:41219091-41219457 | Common:1; Rare:94 | ||||
| chr19:41262355-41262566 | Rare:40 | ||||
| chr19:41310112-41310279 | Rare:67 | ||||
| chr19:41363801-41363970 | Common:1; Rare:57; Clinvar:1 | ||||
| chr19:41364100-41364311 | Common:1; Rare:65; Clinvar:1 | ||||
| chr19:41397324-41397606 | Common:4; Rare:73 | ||||
| chr19:41860038-41860289 | Common:1; Rare:95; Clinvar:3; Clinvar (benign):2 |