| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59155129-59155523 | Common:2; Rare:93 | ||||
| chr17:59619563-59620058 | Common:3; Rare:175 | ||||
| chr17:59707390-59707745 | Common:3; Rare:98; Clinvar (benign):4 | ||||
| chr17:59892891-59893149 | Rare:76 | ||||
| chr17:59964706-59965092 | Common:2; Rare:118 | ||||
| chr17:60526160-60526266 | Rare:42 | ||||
| chr17:63600773-63600929 | Rare:41; Clinvar:2 | ||||
| chr17:63601177-63601198 | Rare:6; Clinvar:1 | ||||
| chr17:63773417-63773850 | Common:2; Rare:143 | ||||
| chr17:63774048-63774370 | Common:10; Rare:132 | ||||
| chr17:63821588-63821849 | Rare:98 | ||||
| chr17:63827057-63827513 | Common:5; Rare:132 | ||||
| chr17:64130026-64130348 | Common:5; Rare:85 | ||||
| chr17:64497034-64497130 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:67245165-67245286 | Rare:41 |