| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19192563-19192978 | Common:2; Rare:108 | ||||
| chr19:19320476-19320858 | Common:4; Rare:141 | ||||
| chr19:19516152-19516331 | Rare:108; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19628169-19628293 | Rare:31 | ||||
| chr19:19643569-19643693 | Common:3; Rare:40 | ||||
| chr19:19668720-19668966 | Common:3; Rare:80 | ||||
| chr19:19821646-19821866 | Common:1; Rare:73 | ||||
| chr19:19900795-19900986 | Common:1; Rare:47 | ||||
| chr19:20661488-20661755 | Common:7; Rare:79 | ||||
| chr19:21141886-21142132 | Rare:65 | ||||
| chr19:21505495-21505622 | Rare:27 | ||||
| chr19:22052361-22052513 | Common:1; Rare:21 | ||||
| chr19:22634117-22634346 | Common:7; Rare:67 | ||||
| chr19:29212904-29213216 | Common:3; Rare:84 | ||||
| chr19:29606187-29606323 | Rare:45 |