| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59120711-59121259 | Common:2; Rare:138 | ||||
| chr17:59153832-59154143 | Common:2; Rare:48 | ||||
| chr17:59327129-59328955 | Common:11; Rare:419 | ||||
| chr17:59332289-59332952 | Rare:259 | ||||
| chr17:59406719-59407117 | Common:4; Rare:76 | ||||
| chr17:59456920-59457390 | Rare:78 | ||||
| chr17:59680957-59681632 | Common:1; Rare:189; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr17:59681728-59682758 | Rare:351 | ||||
| chr17:59685942-59686838 | Common:6; Rare:241 | ||||
| chr17:59686777-59687759 | Common:1; Rare:300 | ||||
| chr17:59688099-59688620 | Common:3; Rare:214 | ||||
| chr17:59690212-59690879 | Common:1; Rare:134 | ||||
| chr17:59690823-59691623 | Common:1; Rare:215 | ||||
| chr17:59692516-59692916 | Common:1; Rare:123 | ||||
| chr17:59693313-59693929 | Common:8; Rare:246; Clinvar (pathogenic):1 |