| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49641812-49642280 | Rare:243 | ||||
| chr19:49664170-49664894 | Common:4; Rare:451 | ||||
| chr19:49665036-49665361 | Common:1; Rare:57 | ||||
| chr19:49665476-49666057 | Common:18; Rare:693; Clinvar (pathogenic):3 | ||||
| chr19:49672014-49673188 | Common:3; Rare:404 | ||||
| chr19:49676299-49677734 | Common:13; Rare:765 | ||||
| chr19:49712293-49712688 | Common:5; Rare:153 | ||||
| chr19:49766247-49766485 | Rare:72 | ||||
| chr19:49766396-49767301 | Common:6; Rare:496 | ||||
| chr19:49808610-49809100 | Common:7; Rare:272; Clinvar:2 | ||||
| chr19:49809242-49809405 | Common:1; Rare:42 | ||||
| chr19:49813150-49813560 | Common:2; Rare:167 | ||||
| chr19:49813470-49813770 | Common:1; Rare:64 | ||||
| chr19:49817470-49817638 | Common:1; Rare:42 | ||||
| chr19:49817944-49818372 | Common:8; Rare:218; Clinvar:6; Clinvar (benign):2 |