| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74431895-74432211 | Common:1; Rare:123 | ||||
| chr17:74432554-74432754 | Common:4; Rare:44 | ||||
| chr17:74442861-74443159 | Common:5; Rare:77 | ||||
| chr17:74465849-74465980 | Common:4; Rare:87 | ||||
| chr17:74466351-74466486 | Rare:34 | ||||
| chr17:74466546-74466826 | Rare:75 | ||||
| chr17:74467082-74467364 | Common:1; Rare:53 | ||||
| chr17:74531432-74531730 | Common:2; Rare:68 | ||||
| chr17:74546064-74546237 | Rare:33 | ||||
| chr17:74748342-74748725 | Common:6; Rare:137 | ||||
| chr17:74776211-74776543 | Common:4; Rare:102 | ||||
| chr17:74872903-74873048 | Common:2; Rare:61; Clinvar (pathogenic):1 | ||||
| chr17:74873349-74873733 | Common:6; Rare:126 | ||||
| chr17:75012438-75012766 | Common:2; Rare:86 | ||||
| chr17:75012859-75013118 | Common:2; Rare:71 |