| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68308630-68308921 | Common:5; Rare:71 | ||||
| chr17:68554797-68554916 | Common:1; Rare:28; Clinvar (pathogenic):1 | ||||
| chr17:68821407-68821622 | Common:1; Rare:31 | ||||
| chr17:70128849-70129049 | Rare:59 | ||||
| chr17:70382631-70382749 | Rare:25 | ||||
| chr17:70703670-70703915 | Common:4; Rare:66 | ||||
| chr17:70835255-70835332 | Common:2; Rare:11 | ||||
| chr17:72115800-72115961 | Rare:28 | ||||
| chr17:72116012-72116024 | Rare:2 | ||||
| chr17:72121653-72121781 | Rare:18; Clinvar (benign):1 | ||||
| chr17:72339545-72339656 | Rare:23 | ||||
| chr17:72342576-72342710 | Rare:31 | ||||
| chr17:72592801-72593048 | Common:1; Rare:67 | ||||
| chr17:72603145-72603351 | Common:2; Rare:47 | ||||
| chr17:73199666-73199945 | Common:2; Rare:53; Clinvar:1 |