| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4558115-4558438 | Common:3; Rare:74 | ||||
| chr19:4639214-4639583 | Common:1; Rare:125 | ||||
| chr19:4831663-4831867 | Common:2; Rare:56 | ||||
| chr19:4867619-4867825 | Common:3; Rare:62 | ||||
| chr19:5622711-5623185 | Common:5; Rare:188 | ||||
| chr19:5680685-5681169 | Rare:134 | ||||
| chr19:5978078-5978370 | Common:3; Rare:109 | ||||
| chr19:6393125-6393227 | Common:2; Rare:23 | ||||
| chr19:6416839-6417019 | Common:1; Rare:66 | ||||
| chr19:7489006-7489103 | Rare:44 | ||||
| chr19:7535574-7535791 | Common:3; Rare:79 | ||||
| chr19:7561077-7561287 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:7629523-7629848 | Common:5; Rare:117; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7903628-7903912 | Rare:92 | ||||
| chr19:7920149-7920364 | Rare:75 |