| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74748414-74748666 | Common:4; Rare:91 | ||||
| chr17:74776250-74776550 | Common:4; Rare:98 | ||||
| chr17:75046942-75047171 | Common:1; Rare:68 | ||||
| chr17:75205370-75205734 | Common:1; Rare:110 | ||||
| chr17:75218049-75218259 | Rare:42 | ||||
| chr17:75261574-75261935 | Common:4; Rare:114; Clinvar (benign):2 | ||||
| chr17:75271146-75271379 | Common:2; Rare:43 | ||||
| chr17:75289377-75289572 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:75393745-75394008 | Common:1; Rare:64 | ||||
| chr17:75515427-75515647 | Common:3; Rare:65 | ||||
| chr17:75621935-75622069 | Common:1; Rare:46 | ||||
| chr17:75633934-75634107 | Common:1; Rare:38 | ||||
| chr17:75667147-75667462 | Common:5; Rare:102 | ||||
| chr17:75720980-75721369 | Common:5; Rare:91 | ||||
| chr17:75756452-75756783 | Rare:134; Clinvar:3; Clinvar (benign):1 |