| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69339253-69339445 | Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:69339542-69339821 | Common:1; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:69408567-69408719 | Common:1; Rare:29 | ||||
| chr16:69424340-69424822 | Common:3; Rare:137 | ||||
| chr16:69565707-69566005 | Common:4; Rare:123 | ||||
| chr16:69726443-69726508 | Rare:23 | ||||
| chr16:69726553-69726593 | Rare:12 | ||||
| chr16:69762266-69762553 | Common:3; Rare:90 | ||||
| chr16:70114118-70114402 | Common:3; Rare:100 | ||||
| chr16:70145633-70145795 | Rare:18 | ||||
| chr16:70173447-70173536 | Rare:14 | ||||
| chr16:70251937-70252008 | Common:1; Rare:25 | ||||
| chr16:70289440-70289767 | Common:3; Rare:135; Clinvar:1 | ||||
| chr16:70294706-70294911 | Common:2; Rare:63 | ||||
| chr16:70299136-70299258 | Rare:27 |