| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48944736-48944850 | Rare:48 | ||||
| chr17:49708148-49708327 | Common:1; Rare:54 | ||||
| chr17:49788358-49788724 | Common:2; Rare:110 | ||||
| chr17:50186429-50186690 | Common:2; Rare:64; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:50188976-50189172 | Rare:47; Clinvar:1 | ||||
| chr17:50194429-50194828 | Common:3; Rare:118; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50196925-50197046 | Common:2; Rare:29; Clinvar (benign):1 | ||||
| chr17:50373160-50373264 | Common:3; Rare:44 | ||||
| chr17:50719444-50719652 | Common:1; Rare:82 | ||||
| chr17:51260139-51260598 | Common:3; Rare:172 | ||||
| chr17:54968608-54968800 | Common:3; Rare:91 | ||||
| chr17:57084980-57085092 | Rare:38 | ||||
| chr17:57849995-57850274 | Common:1; Rare:92 | ||||
| chr17:57988122-57988512 | Common:5; Rare:117 | ||||
| chr17:58352137-58352458 | Common:6; Rare:128 |