| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6393105-6393270 | Common:3; Rare:42 | ||||
| chr19:6393366-6393769 | Common:5; Rare:119 | ||||
| chr19:6416846-6417019 | Common:1; Rare:61 | ||||
| chr19:6710839-6711065 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:7395005-7395203 | Common:6; Rare:63 | ||||
| chr19:7488997-7489123 | Rare:57 | ||||
| chr19:7534103-7534213 | Common:3; Rare:29; Clinvar (benign):1 | ||||
| chr19:7535569-7535787 | Common:3; Rare:79 | ||||
| chr19:7629520-7629854 | Common:5; Rare:121; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7637024-7637143 | Common:2; Rare:41; Clinvar (benign):1 | ||||
| chr19:7851549-7851699 | Common:1; Rare:32 | ||||
| chr19:7874284-7874489 | Rare:54 | ||||
| chr19:7903582-7903904 | Rare:97 | ||||
| chr19:7925525-7925777 | Common:2; Rare:65 | ||||
| chr19:7943606-7943990 | Rare:115 |