| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12881368-12881596 | Rare:45 | ||||
| chr19:12890895-12891207 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:12933680-12933828 | Common:1; Rare:52 | ||||
| chr19:12940238-12940654 | Rare:129 | ||||
| chr19:12952801-12953051 | Rare:62 | ||||
| chr19:13150225-13150457 | Common:1; Rare:79 | ||||
| chr19:13731511-13731785 | Common:6; Rare:68 | ||||
| chr19:13747631-13747942 | Common:2; Rare:116 | ||||
| chr19:13774711-13774859 | Common:1; Rare:55 | ||||
| chr19:13906045-13906341 | Rare:68 | ||||
| chr19:13963644-13963966 | Common:1; Rare:93 | ||||
| chr19:14057560-14057754 | Common:3; Rare:47 | ||||
| chr19:14136573-14136744 | Common:1; Rare:37 | ||||
| chr19:14419281-14419570 | Rare:67 | ||||
| chr19:14518388-14518763 | Common:6; Rare:150 |