| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:16496142-16496424 | Common:2; Rare:74 | ||||
| chr19:16542423-16542583 | Common:2; Rare:38 | ||||
| chr19:17215263-17215402 | Common:2; Rare:50 | ||||
| chr19:17267141-17267492 | Common:3; Rare:72 | ||||
| chr19:18152979-18153277 | Common:1; Rare:94 | ||||
| chr19:18323029-18323232 | Common:3; Rare:68 | ||||
| chr19:18571660-18571897 | Common:2; Rare:100 | ||||
| chr19:18919335-18919738 | Common:2; Rare:144 | ||||
| chr19:19033448-19033658 | Common:2; Rare:71 | ||||
| chr19:19192115-19192262 | Common:1; Rare:48 | ||||
| chr19:19192589-19192991 | Common:2; Rare:103 | ||||
| chr19:19516176-19516293 | Rare:73; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19821700-19821906 | Common:1; Rare:69 | ||||
| chr19:23687136-23687336 | Common:4; Rare:48 | ||||
| chr19:32971916-32972266 | Common:4; Rare:100 |