| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:3573070-3573909 | Common:2; Rare:544 | ||||
| chr19:3606220-3606510 | Common:2; Rare:58 | ||||
| chr19:3626632-3627305 | Common:11; Rare:385 | ||||
| chr19:3708281-3708477 | Common:2; Rare:63 | ||||
| chr19:3708683-3708831 | Common:1; Rare:31 | ||||
| chr19:3721586-3721779 | Common:2; Rare:37 | ||||
| chr19:3761586-3761821 | Common:4; Rare:133 | ||||
| chr19:3762612-3762756 | Common:1; Rare:54 | ||||
| chr19:3762681-3762943 | Common:3; Rare:152 | ||||
| chr19:3785270-3786080 | Common:9; Rare:273 | ||||
| chr19:3786260-3786610 | Common:4; Rare:99 | ||||
| chr19:3969540-3970020 | Rare:223 | ||||
| chr19:3970813-3971452 | Common:6; Rare:445 | ||||
| chr19:3981810-3982130 | Common:2; Rare:136; Clinvar (benign):2 | ||||
| chr19:3982252-3982887 | Common:6; Rare:445; Clinvar:3; Clinvar (benign):6 |