| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:46923091-46923187 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189102-47189330 | Common:1; Rare:66 | ||||
| chr17:47323861-47324009 | Common:2; Rare:53 | ||||
| chr17:47649614-47649965 | Common:1; Rare:134 | ||||
| chr17:47693834-47694067 | Common:1; Rare:40 | ||||
| chr17:47895955-47896281 | Rare:100 | ||||
| chr17:47941371-47941732 | Rare:99; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048048-48048405 | Rare:98 | ||||
| chr17:48048599-48048646 | Common:1; Rare:8 | ||||
| chr17:48048653-48048857 | Common:3; Rare:33 | ||||
| chr17:48107412-48107599 | Common:4; Rare:47 | ||||
| chr17:48430230-48430377 | Rare:44 | ||||
| chr17:48544454-48544847 | Common:3; Rare:156 | ||||
| chr17:48590236-48590364 | Common:1; Rare:28 | ||||
| chr17:48908269-48908407 | Common:2; Rare:32 |