| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68530038-68530154 | Common:4; Rare:52 | ||||
| chr16:68539142-68539406 | Common:4; Rare:117 | ||||
| chr16:69132532-69132697 | Rare:63 | ||||
| chr16:69339548-69339845 | Common:1; Rare:127; Clinvar (benign):1 | ||||
| chr16:69424363-69424678 | Common:1; Rare:81 | ||||
| chr16:69726431-69726524 | Common:1; Rare:32 | ||||
| chr16:69726537-69726593 | Rare:17 | ||||
| chr16:69754892-69755103 | Rare:79 | ||||
| chr16:69762265-69762381 | Common:1; Rare:29 | ||||
| chr16:70114127-70114376 | Common:3; Rare:89 | ||||
| chr16:70289440-70289752 | Common:1; Rare:124; Clinvar:1 | ||||
| chr16:70299078-70299307 | Common:1; Rare:53 | ||||
| chr16:70346735-70346994 | Common:2; Rare:123 | ||||
| chr16:70454353-70454620 | Common:1; Rare:70 | ||||
| chr16:70523486-70523882 | Common:3; Rare:140; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |