| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48363913-48364104 | Common:2; Rare:62 | ||||
| chr19:48445866-48446019 | Rare:51 | ||||
| chr19:48446325-48446468 | Rare:64 | ||||
| chr19:48469054-48469399 | Common:3; Rare:100 | ||||
| chr19:48619139-48619573 | Common:1; Rare:145 | ||||
| chr19:48624209-48624414 | Common:1; Rare:60 | ||||
| chr19:48872218-48872437 | Common:2; Rare:71 | ||||
| chr19:48918414-48919125 | Common:7; Rare:207 | ||||
| chr19:48933540-48933702 | Common:3; Rare:44 | ||||
| chr19:48965426-48965593 | Rare:51; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:48993148-48993556 | Common:4; Rare:177; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:49064981-49065179 | Rare:49 | ||||
| chr19:49085122-49085515 | Common:3; Rare:162 | ||||
| chr19:49114293-49114416 | Common:1; Rare:32 | ||||
| chr19:49115035-49115141 | Rare:25 |