| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49590220-49590537 | Common:1; Rare:108 | ||||
| chr19:49591021-49591258 | Common:3; Rare:52 | ||||
| chr19:49591400-49591700 | Common:9; Rare:82 | ||||
| chr19:49591831-49591985 | Rare:28 | ||||
| chr19:49640070-49640336 | Common:1; Rare:83 | ||||
| chr19:49640496-49640661 | Rare:34 | ||||
| chr19:49641791-49642304 | Rare:141 | ||||
| chr19:49664469-49664660 | Rare:83 | ||||
| chr19:49665505-49665665 | Common:1; Rare:60 | ||||
| chr19:49665761-49666064 | Common:3; Rare:145; Clinvar (pathogenic):1 | ||||
| chr19:49666240-49666362 | Rare:28 | ||||
| chr19:49676144-49676194 | Rare:11 | ||||
| chr19:49676359-49676550 | Common:2; Rare:41 | ||||
| chr19:49676618-49676999 | Common:1; Rare:91 | ||||
| chr19:49677156-49677369 | Common:1; Rare:80 |