| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41009127-41009810 | Common:7; Rare:205 | ||||
| chr17:41505601-41505907 | Common:1; Rare:51 | ||||
| chr17:41524160-41524730 | Common:4; Rare:160; Clinvar:1 | ||||
| chr17:41524840-41525271 | Common:1; Rare:139; Clinvar:2 | ||||
| chr17:41525365-41525745 | Common:5; Rare:114 | ||||
| chr17:41525900-41526418 | Common:5; Rare:221 | ||||
| chr17:41527823-41528655 | Common:7; Rare:336; Clinvar:6 | ||||
| chr17:41688537-41689027 | Common:7; Rare:475 | ||||
| chr17:41689186-41689367 | Common:3; Rare:77 | ||||
| chr17:41689280-41690660 | Common:7; Rare:626 | ||||
| chr17:41772184-41772537 | Common:3; Rare:139 | ||||
| chr17:41785110-41785560 | Common:3; Rare:280 | ||||
| chr17:41785809-41786248 | Common:6; Rare:191 | ||||
| chr17:41786349-41787163 | Common:7; Rare:323; Clinvar:8; Clinvar (benign):6 | ||||
| chr17:41811870-41812530 | Common:3; Rare:566 |