| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69339527-69339831 | Common:1; Rare:136; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:69424334-69424707 | Common:3; Rare:98 | ||||
| chr16:69424754-69424852 | Rare:25 | ||||
| chr16:69565866-69565981 | Common:2; Rare:47 | ||||
| chr16:69566193-69566331 | Common:1; Rare:37 | ||||
| chr16:69726444-69726727 | Common:3; Rare:75 | ||||
| chr16:69762141-69762387 | Common:1; Rare:69 | ||||
| chr16:70114161-70114381 | Common:2; Rare:78 | ||||
| chr16:70265021-70265292 | Common:1; Rare:77; Clinvar:3; Clinvar (benign):3 | ||||
| chr16:70289419-70289656 | Rare:82; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:70346790-70346982 | Common:2; Rare:98 | ||||
| chr16:70454535-70454619 | Rare:19 | ||||
| chr16:70523532-70523844 | Common:3; Rare:100; Clinvar (pathogenic):1 | ||||
| chr16:71289130-71289194 | Rare:13 | ||||
| chr16:71289207-71289276 | Rare:14 |