| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:73232230-73232722 | Common:3; Rare:179 | ||||
| chr17:74213319-74213588 | Common:4; Rare:62 | ||||
| chr17:74431251-74431385 | Rare:35 | ||||
| chr17:74748417-74748632 | Common:2; Rare:71 | ||||
| chr17:74776281-74776544 | Common:4; Rare:87 | ||||
| chr17:75012602-75012700 | Rare:26 | ||||
| chr17:75047010-75047320 | Common:2; Rare:99 | ||||
| chr17:75109878-75110010 | Common:1; Rare:39 | ||||
| chr17:75130764-75131096 | Common:2; Rare:116 | ||||
| chr17:75131440-75131808 | Common:4; Rare:145 | ||||
| chr17:75182836-75183206 | Common:2; Rare:132 | ||||
| chr17:75205367-75205734 | Common:1; Rare:112 | ||||
| chr17:75261590-75261951 | Common:4; Rare:118; Clinvar (benign):3 | ||||
| chr17:75271146-75271298 | Common:1; Rare:33 | ||||
| chr17:75289387-75289613 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 |