| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46023050-46023125 | Rare:22 | ||||
| chr19:46303416-46303670 | Common:1; Rare:42 | ||||
| chr19:46346941-46347215 | Common:3; Rare:94 | ||||
| chr19:46495861-46496005 | Rare:43 | ||||
| chr19:46600913-46601012 | Common:1; Rare:41 | ||||
| chr19:46601076-46601416 | Common:3; Rare:107; Clinvar (benign):1 | ||||
| chr19:46746006-46746068 | Common:3; Rare:19 | ||||
| chr19:47112150-47112378 | Rare:69 | ||||
| chr19:47256472-47256577 | Rare:39 | ||||
| chr19:47289681-47290033 | Common:3; Rare:62 | ||||
| chr19:47349077-47349411 | Rare:96 | ||||
| chr19:47484261-47484318 | Rare:14 | ||||
| chr19:47497477-47497740 | Common:1; Rare:50 | ||||
| chr19:47512756-47512865 | Rare:24 | ||||
| chr19:47745394-47745587 | Common:1; Rare:88 |