| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1971778-1972149 | Common:3; Rare:109 | ||||
| chr16:1972588-1972670 | Common:1; Rare:22 | ||||
| chr16:1983951-1984343 | Common:5; Rare:128; Clinvar (benign):4 | ||||
| chr16:1984387-1984491 | Rare:34; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr16:1992055-1992512 | Common:4; Rare:116 | ||||
| chr16:2009733-2010085 | Common:14; Rare:131 | ||||
| chr16:2010264-2010365 | Rare:27 | ||||
| chr16:2019634-2019841 | Common:2; Rare:55 | ||||
| chr16:2019955-2020046 | Rare:33 | ||||
| chr16:2026795-2026928 | Common:1; Rare:46 | ||||
| chr16:2033741-2033775 | Rare:7 | ||||
| chr16:2047767-2048051 | Rare:138; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:2056035-2056161 | Common:1; Rare:40; Clinvar:2 | ||||
| chr16:2135868-2136157 | Common:1; Rare:138; Clinvar (benign):1 | ||||
| chr16:2136285-2136381 | Common:1; Rare:34 |