| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40750667-40750913 | Common:1; Rare:47 | ||||
| chr19:40750964-40751304 | Common:3; Rare:101 | ||||
| chr19:40777934-40778303 | Common:1; Rare:104 | ||||
| chr19:40850424-40850540 | Common:1; Rare:24 | ||||
| chr19:40990959-40991556 | Common:2; Rare:175 | ||||
| chr19:41009345-41009629 | Common:3; Rare:75; Clinvar (benign):1 | ||||
| chr19:41262371-41262566 | Rare:35 | ||||
| chr19:41264961-41265143 | Common:2; Rare:41 | ||||
| chr19:41363795-41363999 | Common:1; Rare:74; Clinvar:1 | ||||
| chr19:41364137-41364186 | Rare:14 | ||||
| chr19:41397581-41397851 | Common:7; Rare:96; Clinvar (benign):5 | ||||
| chr19:41860033-41860281 | Common:1; Rare:89; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:41883043-41883264 | Common:1; Rare:43 | ||||
| chr19:41884162-41884490 | Rare:93 | ||||
| chr19:42075772-42076227 | Common:5; Rare:133 |