| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19516157-19516323 | Rare:100; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19821692-19821905 | Common:1; Rare:70 | ||||
| chr19:19865714-19865926 | Common:2; Rare:55 | ||||
| chr19:19900745-19901039 | Common:3; Rare:82 | ||||
| chr19:20565746-20565971 | Common:1; Rare:61 | ||||
| chr19:20661524-20661773 | Common:7; Rare:68 | ||||
| chr19:21505373-21505622 | Rare:52 | ||||
| chr19:21836109-21836313 | Rare:80 | ||||
| chr19:23687130-23687343 | Common:4; Rare:54 | ||||
| chr19:24033300-24033550 | Common:7; Rare:56 | ||||
| chr19:29606172-29606323 | Rare:51 | ||||
| chr19:29665311-29665471 | Common:3; Rare:56 | ||||
| chr19:29715192-29715315 | Common:1; Rare:49 | ||||
| chr19:31349217-31349476 | Common:3; Rare:84 | ||||
| chr19:32345536-32345628 | Rare:28 |