| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45730860-45731052 | Common:1; Rare:40 | ||||
| chr19:45768247-45768476 | Rare:99; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:45769203-45769363 | Rare:55 | ||||
| chr19:45769388-45769658 | Common:1; Rare:119 | ||||
| chr19:45770304-45770963 | Common:6; Rare:293; Clinvar:2 | ||||
| chr19:45902615-45902916 | Common:3; Rare:87 | ||||
| chr19:46298063-46298469 | Common:5; Rare:93 | ||||
| chr19:46346951-46347210 | Common:3; Rare:88 | ||||
| chr19:46413419-46413773 | Common:1; Rare:103 | ||||
| chr19:46600908-46601420 | Common:5; Rare:177; Clinvar (benign):1 | ||||
| chr19:46714246-46714399 | Common:1; Rare:24 | ||||
| chr19:46745750-46746074 | Common:4; Rare:67 | ||||
| chr19:46746296-46746602 | Common:4; Rare:87 | ||||
| chr19:46788555-46788629 | Rare:18 | ||||
| chr19:47112146-47112403 | Rare:79 |