| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34677541-34677758 | Common:5; Rare:63 | ||||
| chr19:34734108-34734260 | Common:1; Rare:49 | ||||
| chr19:35248827-35249020 | Common:1; Rare:80 | ||||
| chr19:35545454-35545714 | Common:4; Rare:86 | ||||
| chr19:35628748-35629120 | Common:4; Rare:113 | ||||
| chr19:35648101-35648381 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35745381-35745699 | Rare:94 | ||||
| chr19:35900538-35900731 | Rare:46 | ||||
| chr19:36014192-36014493 | Common:1; Rare:85 | ||||
| chr19:36114842-36114989 | Common:2; Rare:65 | ||||
| chr19:36215073-36215181 | Rare:34 | ||||
| chr19:36379171-36379272 | Common:1; Rare:37 | ||||
| chr19:36489496-36489644 | Common:1; Rare:34 | ||||
| chr19:36528230-36528416 | Common:1; Rare:47 | ||||
| chr19:36573247-36573489 | Common:3; Rare:78 |