| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40417163-40417391 | Common:1; Rare:58 | ||||
| chr19:40420828-40421534 | Common:13; Rare:362 | ||||
| chr19:40432943-40433383 | Common:9; Rare:125 | ||||
| chr19:40433411-40433603 | Common:2; Rare:68 | ||||
| chr19:40433760-40434300 | Common:10; Rare:337 | ||||
| chr19:40445456-40446236 | Common:2; Rare:274 | ||||
| chr19:40531321-40531721 | Common:10; Rare:112 | ||||
| chr19:40603921-40604321 | Rare:132 | ||||
| chr19:40605190-40605560 | Rare:136; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:40605555-40605756 | Rare:113; Clinvar:5; Clinvar (benign):4 | ||||
| chr19:40662750-40663100 | Common:3; Rare:86 | ||||
| chr19:40663274-40663410 | Common:1; Rare:33 | ||||
| chr19:40663470-40664000 | Common:1; Rare:90 | ||||
| chr19:40718770-40719230 | Common:3; Rare:243 | ||||
| chr19:40744545-40745157 | Common:15; Rare:416 |