| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:64497044-64497154 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:64506244-64506394 | Common:3; Rare:66 | ||||
| chr17:64506623-64506794 | Common:2; Rare:66 | ||||
| chr17:65056592-65056897 | Common:4; Rare:120 | ||||
| chr17:67245845-67245932 | Rare:25 | ||||
| chr17:67366446-67366743 | Rare:99 | ||||
| chr17:67717629-67717959 | Common:3; Rare:112 | ||||
| chr17:68035411-68035809 | Common:4; Rare:99 | ||||
| chr17:68247866-68248142 | Common:6; Rare:115 | ||||
| chr17:68259125-68259200 | Rare:26 | ||||
| chr17:69327091-69327327 | Common:2; Rare:79 | ||||
| chr17:69414617-69414754 | Rare:28 | ||||
| chr17:73232100-73232707 | Common:4; Rare:230 | ||||
| chr17:74203396-74203745 | Common:3; Rare:106 | ||||
| chr17:74361890-74362153 | Common:1; Rare:50 |