| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45507228-45507516 | Common:1; Rare:74 | ||||
| chr19:45730869-45731084 | Common:1; Rare:50 | ||||
| chr19:46413552-46413739 | Common:1; Rare:60 | ||||
| chr19:46600978-46601402 | Common:4; Rare:141 | ||||
| chr19:46745889-46746066 | Common:3; Rare:38 | ||||
| chr19:47112166-47112333 | Rare:52 | ||||
| chr19:47256472-47256577 | Rare:39 | ||||
| chr19:47484191-47484380 | Common:1; Rare:60 | ||||
| chr19:47745440-47745559 | Rare:58 | ||||
| chr19:48170292-48170696 | Common:2; Rare:107 | ||||
| chr19:48619139-48619534 | Common:1; Rare:131 | ||||
| chr19:48872195-48872426 | Common:2; Rare:67 | ||||
| chr19:48900200-48900367 | Common:1; Rare:60 | ||||
| chr19:48993285-48993909 | Common:8; Rare:210; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:49085111-49085492 | Common:3; Rare:152 |