| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3535652-3535791 | Rare:44 | ||||
| chr17:3636189-3636545 | Common:5; Rare:110; Clinvar (benign):2 | ||||
| chr17:3636677-3636775 | Common:1; Rare:26; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:3667985-3668276 | Rare:67 | ||||
| chr17:3668511-3668929 | Common:3; Rare:164 | ||||
| chr17:3723539-3723591 | Rare:16 | ||||
| chr17:3723696-3724009 | Common:1; Rare:173 | ||||
| chr17:3845821-3845887 | Rare:9 | ||||
| chr17:3846172-3846478 | Common:1; Rare:101 | ||||
| chr17:4142921-4143268 | Common:3; Rare:125 | ||||
| chr17:4143561-4143847 | Common:5; Rare:154 | ||||
| chr17:4144023-4144215 | Common:2; Rare:66 | ||||
| chr17:4180728-4180974 | Common:2; Rare:40 | ||||
| chr17:4263688-4263728 | Rare:15 | ||||
| chr17:4263851-4264115 | Common:1; Rare:109 |