| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89972478-89972658 | Common:1; Rare:66 | ||||
| chr16:90022564-90022712 | Rare:58 | ||||
| chr17:714785-714936 | Common:2; Rare:54 | ||||
| chr17:732315-732624 | Common:2; Rare:106 | ||||
| chr17:752146-752368 | Common:2; Rare:89 | ||||
| chr17:1400048-1400356 | Common:3; Rare:126 | ||||
| chr17:1516588-1516984 | Common:2; Rare:139 | ||||
| chr17:1673091-1673466 | Common:2; Rare:87; Clinvar:2 | ||||
| chr17:1684780-1684879 | Common:1; Rare:41; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1716204-1716543 | Common:3; Rare:103 | ||||
| chr17:1829788-1830096 | Common:8; Rare:129 | ||||
| chr17:2071588-2071813 | Common:2; Rare:62 | ||||
| chr17:2303468-2303637 | Rare:61 | ||||
| chr17:2303728-2303987 | Common:2; Rare:97 | ||||
| chr17:2336423-2336563 | Rare:53 |