| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47941365-47941732 | Rare:102; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048045-48048405 | Common:1; Rare:98 | ||||
| chr17:48048602-48048813 | Common:4; Rare:30 | ||||
| chr17:48544454-48544517 | Common:1; Rare:19 | ||||
| chr17:48544536-48544667 | Rare:65 | ||||
| chr17:48590153-48590506 | Common:2; Rare:75 | ||||
| chr17:48908269-48908407 | Common:2; Rare:32 | ||||
| chr17:48944765-48944920 | Common:2; Rare:54 | ||||
| chr17:49210227-49210720 | Common:3; Rare:84 | ||||
| chr17:49646446-49646771 | Common:2; Rare:57 | ||||
| chr17:49788557-49788784 | Common:1; Rare:76 | ||||
| chr17:50165930-50166041 | Common:2; Rare:42; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:50188621-50189011 | Rare:105; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):5 | ||||
| chr17:50189206-50189493 | Rare:64; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:50192474-50192684 | Common:1; Rare:45; Clinvar:3; Clinvar (benign):4 |