| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50384283-50384389 | Rare:40; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:50476238-50476538 | Rare:139 | ||||
| chr19:50511147-50511272 | Rare:43 | ||||
| chr19:50723181-50723600 | Common:2; Rare:115 | ||||
| chr19:50804584-50804877 | Common:5; Rare:90 | ||||
| chr19:51366335-51366607 | Common:8; Rare:76; Clinvar (benign):2 | ||||
| chr19:51751852-51751987 | Common:2; Rare:28 | ||||
| chr19:51887866-51888052 | Rare:65 | ||||
| chr19:52008160-52008314 | Rare:47 | ||||
| chr19:52028313-52028462 | Common:3; Rare:37 | ||||
| chr19:52048704-52048914 | Common:2; Rare:71 | ||||
| chr19:52369849-52369966 | Common:2; Rare:41 | ||||
| chr19:52397677-52397889 | Common:5; Rare:61 | ||||
| chr19:52535862-52536011 | Common:2; Rare:63 | ||||
| chr19:52690455-52690781 | Common:6; Rare:77 |