| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47188839-47188935 | Rare:14 | ||||
| chr17:47189202-47189340 | Common:1; Rare:43 | ||||
| chr17:47323864-47324034 | Common:1; Rare:64 | ||||
| chr17:47324515-47324546 | Rare:11 | ||||
| chr17:47530851-47531293 | Common:2; Rare:119 | ||||
| chr17:47618244-47618370 | Rare:29 | ||||
| chr17:47618845-47619153 | Rare:64 | ||||
| chr17:47649420-47649450 | Rare:5 | ||||
| chr17:47649498-47649987 | Common:1; Rare:176 | ||||
| chr17:47680014-47680318 | Common:1; Rare:61 | ||||
| chr17:47695045-47695075 | Rare:4 | ||||
| chr17:47695441-47695673 | Common:2; Rare:53 | ||||
| chr17:47831507-47831656 | Rare:40 | ||||
| chr17:47896484-47896558 | Rare:17 | ||||
| chr17:47941335-47941761 | Rare:112; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 |