| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35843879-35844154 | Rare:73; Clinvar (pathogenic):2 | ||||
| chr19:35861173-35861398 | Rare:64 | ||||
| chr19:35903748-35903873 | Common:1; Rare:48 | ||||
| chr19:35911872-35912272 | Common:5; Rare:71 | ||||
| chr19:35931421-35931822 | Common:2; Rare:114 | ||||
| chr19:35936220-35936427 | Common:1; Rare:48 | ||||
| chr19:35987344-35987522 | Common:6; Rare:63 | ||||
| chr19:36127975-36128241 | Common:3; Rare:53 | ||||
| chr19:36128310-36128700 | Common:2; Rare:74 | ||||
| chr19:36132550-36132750 | Common:2; Rare:48 | ||||
| chr19:36136353-36136684 | Common:2; Rare:87 | ||||
| chr19:36137070-36137201 | Rare:21 | ||||
| chr19:36182550-36183250 | Rare:159 | ||||
| chr19:37898768-37898896 | Common:1; Rare:23 | ||||
| chr19:37979896-37980038 | Common:3; Rare:24 |