| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35716759-35717112 | Common:3; Rare:66 | ||||
| chr19:35776375-35776932 | Common:5; Rare:153 | ||||
| chr19:35861179-35861417 | Rare:65 | ||||
| chr19:35931442-35931791 | Common:1; Rare:98 | ||||
| chr19:35936220-35936412 | Common:1; Rare:41 | ||||
| chr19:36097006-36097406 | Common:3; Rare:191; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:36127851-36128145 | Common:7; Rare:56 | ||||
| chr19:36128474-36128650 | Common:2; Rare:40 | ||||
| chr19:36257466-36257866 | Common:10; Rare:194 | ||||
| chr19:36331645-36331975 | Common:2; Rare:83 | ||||
| chr19:36797270-36797580 | Common:1; Rare:67 | ||||
| chr19:37304206-37304606 | Common:11; Rare:288 | ||||
| chr19:38003428-38003895 | Common:9; Rare:167 | ||||
| chr19:38004560-38004780 | Common:2; Rare:49 | ||||
| chr19:38209662-38209795 | Rare:38 |