| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:16197653-16197999 | Common:4; Rare:110 | ||||
| chr19:16324586-16324931 | Common:2; Rare:102 | ||||
| chr19:16471345-16471470 | Rare:19 | ||||
| chr19:16471925-16472307 | Common:5; Rare:116 | ||||
| chr19:16496034-16496472 | Common:2; Rare:133; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:16542206-16542722 | Common:2; Rare:174 | ||||
| chr19:16542850-16542911 | Rare:10 | ||||
| chr19:16572291-16572699 | Common:5; Rare:153 | ||||
| chr19:16587071-16587196 | Common:2; Rare:28 | ||||
| chr19:16587413-16587938 | Common:2; Rare:82 | ||||
| chr19:16628114-16628667 | Common:1; Rare:212 | ||||
| chr19:16628845-16629087 | Rare:64 | ||||
| chr19:16659781-16659953 | Common:1; Rare:76 | ||||
| chr19:16660076-16660435 | Common:3; Rare:134 | ||||
| chr19:16660999-16661227 | Common:2; Rare:73 |