| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6740809-6740935 | Rare:27 | ||||
| chr19:7069640-7069714 | Rare:20 | ||||
| chr19:7294412-7294554 | Common:1; Rare:40 | ||||
| chr19:7395033-7395203 | Common:4; Rare:55 | ||||
| chr19:7488993-7489104 | Rare:51 | ||||
| chr19:7535574-7535780 | Common:3; Rare:74 | ||||
| chr19:7629514-7629859 | Common:5; Rare:124; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636981-7637145 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr19:7903536-7903923 | Rare:124 | ||||
| chr19:7910765-7911057 | Common:1; Rare:125 | ||||
| chr19:7920235-7920375 | Rare:63 | ||||
| chr19:7943627-7944000 | Rare:105 | ||||
| chr19:8005498-8005821 | Common:1; Rare:113 | ||||
| chr19:8321324-8321703 | Common:2; Rare:153 | ||||
| chr19:8343254-8343414 | Rare:37 |