| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:51366307-51366623 | Common:8; Rare:96; Clinvar (benign):2 | ||||
| chr19:51366850-51366984 | Common:1; Rare:26 | ||||
| chr19:51367532-51367899 | Common:1; Rare:114 | ||||
| chr19:51367998-51368159 | Common:1; Rare:65 | ||||
| chr19:51571110-51571376 | Common:5; Rare:74 | ||||
| chr19:51887513-51887668 | Rare:35 | ||||
| chr19:51887670-51888142 | Common:1; Rare:129 | ||||
| chr19:51904580-51904638 | Common:1; Rare:18 | ||||
| chr19:51904815-51904911 | Rare:25 | ||||
| chr19:51904964-51905160 | Common:1; Rare:68 | ||||
| chr19:51926731-51926909 | Common:1; Rare:32 | ||||
| chr19:51926963-51927152 | Rare:38 | ||||
| chr19:51927276-51927427 | Rare:54 | ||||
| chr19:51986767-51987028 | Common:2; Rare:72 | ||||
| chr19:52007927-52007966 | Common:4; Rare:6 |