| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10928589-10928894 | Common:2; Rare:102 | ||||
| chr19:10960601-10961106 | Common:7; Rare:198 | ||||
| chr19:10961186-10961292 | Rare:43 | ||||
| chr19:10961592-10961667 | Rare:16 | ||||
| chr19:11089236-11089542 | Rare:56; Clinvar:12; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:11090294-11090691 | Common:2; Rare:122 | ||||
| chr19:11155710-11156148 | Common:4; Rare:119 | ||||
| chr19:11195239-11195390 | Common:1; Rare:43 | ||||
| chr19:11197497-11197695 | Common:1; Rare:63 | ||||
| chr19:11197723-11198024 | Common:2; Rare:84 | ||||
| chr19:11339566-11339810 | Common:5; Rare:64 | ||||
| chr19:11346161-11346788 | Rare:135 | ||||
| chr19:11374511-11374756 | Common:1; Rare:83 | ||||
| chr19:11374818-11375280 | Common:2; Rare:161 | ||||
| chr19:11381103-11381243 | Rare:49; Clinvar:1; Clinvar (benign):1 |