| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17281854-17282068 | Rare:82 | ||||
| chr19:17282722-17282800 | Rare:24 | ||||
| chr19:17292476-17292707 | Common:2; Rare:55 | ||||
| chr19:17292910-17293277 | Common:4; Rare:59 | ||||
| chr19:17303386-17303660 | Common:2; Rare:66 | ||||
| chr19:17305569-17305656 | Rare:20 | ||||
| chr19:17305657-17305943 | Common:3; Rare:121 | ||||
| chr19:17306041-17306090 | Rare:13 | ||||
| chr19:17306242-17306301 | Common:1; Rare:17 | ||||
| chr19:17309237-17309644 | Common:3; Rare:122 | ||||
| chr19:17334761-17335000 | Common:3; Rare:83 | ||||
| chr19:17336627-17336773 | Rare:27 | ||||
| chr19:17337082-17337139 | Rare:12 | ||||
| chr19:17337223-17337621 | Common:1; Rare:98; Clinvar:1 | ||||
| chr19:17338044-17338090 | Rare:20; Clinvar (benign):2 |