| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69132510-69132686 | Rare:66 | ||||
| chr16:69311096-69311470 | Rare:113 | ||||
| chr16:69339548-69339841 | Common:1; Rare:126; Clinvar (benign):1 | ||||
| chr16:69565681-69566012 | Common:4; Rare:133 | ||||
| chr16:69690720-69690998 | Rare:57; Clinvar:2 | ||||
| chr16:69726431-69726802 | Common:4; Rare:101 | ||||
| chr16:69762267-69762387 | Common:1; Rare:29 | ||||
| chr16:70114136-70114393 | Common:3; Rare:90 | ||||
| chr16:70289419-70289648 | Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:70299111-70299239 | Rare:27 | ||||
| chr16:70346815-70346994 | Common:2; Rare:86 | ||||
| chr16:70523503-70523886 | Common:3; Rare:129; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70560981-70561231 | Common:2; Rare:60 | ||||
| chr16:71808336-71808474 | Rare:47 | ||||
| chr16:71808739-71809344 | Common:4; Rare:222 |