| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19192614-19192968 | Common:2; Rare:85 | ||||
| chr19:19516172-19516285 | Rare:69; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19900745-19900970 | Common:1; Rare:65 | ||||
| chr19:21141735-21142085 | Common:1; Rare:90 | ||||
| chr19:21767547-21767712 | Common:1; Rare:40 | ||||
| chr19:29213143-29213295 | Common:3; Rare:51 | ||||
| chr19:29665253-29665466 | Common:4; Rare:78 | ||||
| chr19:29715214-29715328 | Common:1; Rare:47 | ||||
| chr19:32971928-32972284 | Common:4; Rare:101 | ||||
| chr19:33521765-33521956 | Common:1; Rare:57; Clinvar:3 | ||||
| chr19:34254523-34254602 | Rare:20 | ||||
| chr19:34677263-34677308 | Common:1; Rare:10 | ||||
| chr19:34677595-34677758 | Common:4; Rare:42 | ||||
| chr19:35138648-35138883 | Rare:58 | ||||
| chr19:35139521-35139766 | Common:1; Rare:62 |