| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40750411-40750635 | Common:5; Rare:69 | ||||
| chr19:40751064-40751367 | Common:3; Rare:86 | ||||
| chr19:40798916-40799248 | Common:6; Rare:124 | ||||
| chr19:41219035-41219238 | Rare:36 | ||||
| chr19:41262313-41262583 | Rare:47 | ||||
| chr19:41264703-41264823 | Rare:34 | ||||
| chr19:41310133-41310268 | Rare:53 | ||||
| chr19:41363795-41364014 | Common:1; Rare:80; Clinvar:1 | ||||
| chr19:41364123-41364279 | Rare:50; Clinvar:1 | ||||
| chr19:41860110-41860270 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:41861001-41861209 | Rare:67; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:42075809-42076199 | Rare:110 | ||||
| chr19:42217696-42217842 | Rare:54 | ||||
| chr19:42220128-42220358 | Common:2; Rare:62 | ||||
| chr19:42268232-42268559 | Rare:65 |