| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40348398-40348739 | Common:4; Rare:112 | ||||
| chr19:40425989-40426147 | Common:1; Rare:46 | ||||
| chr19:40444279-40444513 | Common:3; Rare:73 | ||||
| chr19:40465645-40466096 | Common:3; Rare:147 | ||||
| chr19:40715074-40715187 | Rare:30 | ||||
| chr19:40716847-40717358 | Common:2; Rare:162 | ||||
| chr19:40718225-40718251 | Rare:8 | ||||
| chr19:40750564-40750913 | Common:3; Rare:79 | ||||
| chr19:40750926-40751283 | Common:4; Rare:110 | ||||
| chr19:40990973-40991301 | Common:1; Rare:70 | ||||
| chr19:41262336-41262566 | Rare:44 | ||||
| chr19:41363795-41363999 | Common:1; Rare:74; Clinvar:1 | ||||
| chr19:41364123-41364469 | Rare:103; Clinvar:1 | ||||
| chr19:41860038-41860289 | Common:1; Rare:95; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:41884132-41884437 | Rare:73 |