| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49362340-49362490 | Rare:42 | ||||
| chr19:49423646-49423790 | Rare:22 | ||||
| chr19:49451748-49451996 | Common:3; Rare:63 | ||||
| chr19:49453024-49453300 | Common:2; Rare:84 | ||||
| chr19:49453465-49453619 | Rare:48 | ||||
| chr19:49487300-49487644 | Common:5; Rare:123 | ||||
| chr19:49513318-49513393 | Rare:15 | ||||
| chr19:49556938-49557165 | Rare:96 | ||||
| chr19:49580521-49580650 | Rare:46 | ||||
| chr19:49665718-49666020 | Common:3; Rare:139; Clinvar (pathogenic):1 | ||||
| chr19:49690973-49691142 | Rare:37 | ||||
| chr19:49808823-49808997 | Common:1; Rare:57 | ||||
| chr19:49813167-49813339 | Rare:65 | ||||
| chr19:49850923-49851056 | Common:1; Rare:52 | ||||
| chr19:49851058-49851120 | Rare:24 |