| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48872177-48872604 | Common:2; Rare:131 | ||||
| chr19:48872782-48873286 | Common:6; Rare:94 | ||||
| chr19:48899909-48900433 | Common:3; Rare:145 | ||||
| chr19:48933420-48933725 | Common:4; Rare:86 | ||||
| chr19:48933752-48933907 | Common:1; Rare:61 | ||||
| chr19:48954623-48955112 | Common:3; Rare:155 | ||||
| chr19:48955114-48955336 | Common:1; Rare:47 | ||||
| chr19:48964718-48964869 | Common:1; Rare:21 | ||||
| chr19:48965017-48965437 | Common:1; Rare:113; Clinvar:1; Clinvar (pathogenic):5 | ||||
| chr19:48965445-48965745 | Rare:100; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:48993202-48993591 | Common:4; Rare:167; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:48993705-48993954 | Common:5; Rare:81 | ||||
| chr19:49056242-49056348 | Common:2; Rare:61 | ||||
| chr19:49064937-49065165 | Rare:62 | ||||
| chr19:49072670-49072798 | Common:2; Rare:19 |