| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50201408-50201543 | Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:50201553-50201677 | Common:2; Rare:35; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:50372853-50373281 | Common:4; Rare:144 | ||||
| chr17:50426155-50426255 | Rare:24 | ||||
| chr17:50707846-50708081 | Rare:52 | ||||
| chr17:50719478-50719896 | Common:4; Rare:135 | ||||
| chr17:50866057-50866137 | Rare:19 | ||||
| chr17:50866316-50866632 | Common:4; Rare:100 | ||||
| chr17:50867971-50868067 | Rare:19 | ||||
| chr17:51153462-51153662 | Common:1; Rare:42 | ||||
| chr17:51166324-51166623 | Common:3; Rare:80 | ||||
| chr17:51166664-51166954 | Rare:84 | ||||
| chr17:51260332-51260699 | Common:4; Rare:175 | ||||
| chr17:54968292-54968346 | Rare:19 | ||||
| chr17:54968363-54968795 | Common:3; Rare:173 |