| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75261570-75261925 | Common:4; Rare:110; Clinvar (benign):1 | ||||
| chr17:75289365-75289631 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:75667131-75667387 | Common:4; Rare:86 | ||||
| chr17:75779690-75780014 | Common:1; Rare:144 | ||||
| chr17:75784563-75784872 | Common:2; Rare:136 | ||||
| chr17:75878552-75878743 | Common:3; Rare:66 | ||||
| chr17:75979008-75979283 | Rare:79; Clinvar:4 | ||||
| chr17:75979394-75979463 | Rare:19 | ||||
| chr17:76353589-76353675 | Rare:37 | ||||
| chr17:76726435-76726854 | Common:3; Rare:145 | ||||
| chr17:76737318-76737678 | Common:4; Rare:126 | ||||
| chr17:76737876-76738043 | Common:3; Rare:47 | ||||
| chr17:77319431-77319602 | Common:3; Rare:43; Clinvar (benign):3 | ||||
| chr17:77319875-77319935 | Common:1; Rare:12; Clinvar (benign):1 | ||||
| chr17:77320077-77320329 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |