| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76103680-76103876 | Common:5; Rare:70 | ||||
| chr17:76141243-76141496 | Common:1; Rare:62 | ||||
| chr17:76353612-76353677 | Rare:27 | ||||
| chr17:76501379-76501558 | Rare:61; Clinvar (benign):3 | ||||
| chr17:76726469-76726858 | Common:4; Rare:137 | ||||
| chr17:76737325-76737678 | Common:3; Rare:121 | ||||
| chr17:76737864-76738084 | Common:3; Rare:63 | ||||
| chr17:77140641-77141069 | Common:3; Rare:147 | ||||
| chr17:78187035-78187376 | Common:3; Rare:112 | ||||
| chr17:78782219-78782570 | Common:9; Rare:116 | ||||
| chr17:78840740-78841043 | Common:2; Rare:108 | ||||
| chr17:78979866-78980198 | Common:2; Rare:66 | ||||
| chr17:79009696-79009924 | Common:9; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:80035843-80036037 | Common:1; Rare:68 | ||||
| chr17:80220309-80220453 | Rare:57; Clinvar:1; Clinvar (pathogenic):2 |