| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:43417664-43418006 | Common:1; Rare:74 | ||||
| chr19:43618979-43619028 | Rare:5 | ||||
| chr19:43635079-43635398 | Rare:64 | ||||
| chr19:44847586-44847653 | Rare:12 | ||||
| chr19:44987890-44988148 | Common:1; Rare:66 | ||||
| chr19:45484439-45484572 | Rare:29 | ||||
| chr19:45717249-45717548 | Common:1; Rare:92 | ||||
| chr19:45954280-45954394 | Rare:22 | ||||
| chr19:46078865-46079209 | Common:13; Rare:57 | ||||
| chr19:46412078-46412277 | Common:1; Rare:75; Clinvar (pathogenic):1 | ||||
| chr19:46494151-46494326 | Common:1; Rare:56 | ||||
| chr19:46520758-46520921 | Common:4; Rare:38 | ||||
| chr19:46608852-46609152 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):6 | ||||
| chr19:46661997-46662166 | Rare:26 | ||||
| chr19:46860778-46861141 | Common:3; Rare:115 |