| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6731492-6731580 | Common:1; Rare:26 | ||||
| chr19:7395036-7395185 | Common:4; Rare:47 | ||||
| chr19:7488970-7489070 | Rare:51 | ||||
| chr19:7535574-7535740 | Common:3; Rare:55 | ||||
| chr19:7629531-7629848 | Common:5; Rare:113; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636950-7637152 | Common:2; Rare:59; Clinvar (benign):1 | ||||
| chr19:7903571-7903904 | Rare:102 | ||||
| chr19:7910771-7911120 | Common:1; Rare:140 | ||||
| chr19:7920149-7920341 | Rare:59 | ||||
| chr19:7943606-7943990 | Rare:115 | ||||
| chr19:8209229-8209474 | Common:2; Rare:70 | ||||
| chr19:8320859-8320990 | Rare:45 | ||||
| chr19:8321316-8321703 | Common:2; Rare:155 | ||||
| chr19:8364022-8364187 | Common:2; Rare:44 | ||||
| chr19:8390032-8390450 | Common:2; Rare:117 |