| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17334705-17335006 | Common:3; Rare:109 | ||||
| chr19:17336574-17336745 | Rare:41 | ||||
| chr19:17337040-17337173 | Rare:30 | ||||
| chr19:17337269-17337643 | Common:1; Rare:91; Clinvar:1 | ||||
| chr19:17337957-17338205 | Common:1; Rare:92; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:17404135-17404390 | Common:2; Rare:54 | ||||
| chr19:17404718-17404888 | Rare:29 | ||||
| chr19:17405086-17405404 | Common:2; Rare:68 | ||||
| chr19:17405503-17405862 | Common:6; Rare:74 | ||||
| chr19:17405945-17406172 | Common:3; Rare:54; Clinvar:1 | ||||
| chr19:17406283-17406553 | Common:3; Rare:49 | ||||
| chr19:17419686-17420173 | Common:20; Rare:137 | ||||
| chr19:17469825-17470062 | Common:1; Rare:32 | ||||
| chr19:17470296-17470552 | Rare:85 | ||||
| chr19:17511369-17511723 | Common:3; Rare:126 |