| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12156689-12156848 | Common:1; Rare:37 | ||||
| chr19:12162915-12163169 | Rare:73 | ||||
| chr19:12294748-12295059 | Common:1; Rare:84 | ||||
| chr19:12333666-12333856 | Rare:53 | ||||
| chr19:12365612-12365787 | Common:3; Rare:47 | ||||
| chr19:12440959-12441178 | Common:5; Rare:73 | ||||
| chr19:12484733-12484949 | Common:1; Rare:52 | ||||
| chr19:12551387-12551713 | Common:2; Rare:86 | ||||
| chr19:12610681-12610999 | Rare:102 | ||||
| chr19:12666704-12666871 | Rare:66; Clinvar:2 | ||||
| chr19:12681357-12681499 | Common:1; Rare:51 | ||||
| chr19:12681764-12682037 | Common:4; Rare:131; Clinvar (pathogenic):1 | ||||
| chr19:12696586-12696736 | Rare:72 | ||||
| chr19:12722486-12722797 | Common:3; Rare:53 | ||||
| chr19:12723916-12724104 | Common:1; Rare:42 |