| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28845317-28845615 | Common:2; Rare:89; Clinvar (pathogenic):1 | ||||
| chr16:28846196-28846700 | Common:2; Rare:166; Clinvar:7; Clinvar (benign):6 | ||||
| chr16:28863093-28863425 | Common:3; Rare:71 | ||||
| chr16:28863462-28863552 | Rare:19 | ||||
| chr16:28863721-28864007 | Common:3; Rare:75 | ||||
| chr16:28879873-28880066 | Common:3; Rare:57 | ||||
| chr16:28925159-28925375 | Rare:69 | ||||
| chr16:28936579-28936793 | Rare:57 | ||||
| chr16:28950612-28951014 | Common:2; Rare:111 | ||||
| chr16:28974669-28974792 | Rare:56 | ||||
| chr16:29679074-29679144 | Rare:26 | ||||
| chr16:29790498-29790816 | Common:1; Rare:123; Clinvar (benign):2 | ||||
| chr16:29805482-29805679 | Common:1; Rare:91 | ||||
| chr16:29807900-29808144 | Rare:142 | ||||
| chr16:29815998-29816232 | Common:1; Rare:67 |