| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:60677629-60677917 | Common:1; Rare:79 | ||||
| chr17:61399392-61400055 | Common:4; Rare:327 | ||||
| chr17:61400121-61400546 | Common:1; Rare:276; Clinvar (pathogenic):2 | ||||
| chr17:61863437-61863749 | Common:5; Rare:121; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:62065348-62065535 | Common:3; Rare:56 | ||||
| chr17:62423782-62424010 | Common:1; Rare:154 | ||||
| chr17:62478545-62479004 | Common:8; Rare:179 | ||||
| chr17:63550103-63550697 | Common:6; Rare:246 | ||||
| chr17:63600773-63601120 | Rare:130; Clinvar:4 | ||||
| chr17:63621826-63622724 | Common:5; Rare:554 | ||||
| chr17:63699240-63699630 | Rare:143 | ||||
| chr17:63700041-63700293 | Common:2; Rare:101 | ||||
| chr17:63741752-63741993 | Common:6; Rare:203 | ||||
| chr17:63773398-63773865 | Common:4; Rare:280 | ||||
| chr17:63774057-63774298 | Common:18; Rare:217 |