| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58692495-58692746 | Common:3; Rare:134; Clinvar:27; Clinvar (benign):27; Clinvar (pathogenic):2 | ||||
| chr17:59106675-59107146 | Common:3; Rare:156; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:59154976-59155786 | Common:2; Rare:220 | ||||
| chr17:59619558-59620004 | Common:3; Rare:160 | ||||
| chr17:59620008-59620168 | Rare:46 | ||||
| chr17:59647209-59647480 | Rare:47 | ||||
| chr17:59664518-59664904 | Common:4; Rare:61 | ||||
| chr17:59683509-59683753 | Rare:40 | ||||
| chr17:59707362-59707751 | Common:4; Rare:106; Clinvar (benign):6 | ||||
| chr17:59837635-59838104 | Common:2; Rare:71 | ||||
| chr17:59838180-59838231 | Rare:5 | ||||
| chr17:59838240-59838442 | Rare:55 | ||||
| chr17:59892710-59893265 | Common:1; Rare:155 | ||||
| chr17:59958788-59958978 | Rare:25 | ||||
| chr17:60078819-60079014 | Common:4; Rare:86 |