| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35578515-35578736 | Common:3; Rare:107; Clinvar (benign):2 | ||||
| chr17:35587176-35587601 | Rare:200 | ||||
| chr17:35795583-35795831 | Rare:90 | ||||
| chr17:35809194-35809636 | Common:1; Rare:290 | ||||
| chr17:35809872-35810171 | Rare:84 | ||||
| chr17:36486476-36486700 | Common:4; Rare:137 | ||||
| chr17:36534000-36534370 | Rare:135 | ||||
| chr17:36534738-36535080 | Common:6; Rare:244 | ||||
| chr17:36544761-36544994 | Common:7; Rare:147 | ||||
| chr17:36545381-36545700 | Common:4; Rare:201 | ||||
| chr17:36591728-36591923 | Rare:77 | ||||
| chr17:36601489-36601675 | Common:1; Rare:106 | ||||
| chr17:36601740-36602000 | Rare:108 | ||||
| chr17:36936010-36936370 | Common:2; Rare:76 | ||||
| chr17:36948777-36949134 | Common:4; Rare:229 |