| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1965238-1965280 | Common:1; Rare:21 | ||||
| chr16:1971766-1972146 | Common:3; Rare:111 | ||||
| chr16:1983867-1984368 | Common:6; Rare:159; Clinvar (benign):4 | ||||
| chr16:1990107-1990433 | Common:2; Rare:59 | ||||
| chr16:1991104-1991450 | Common:1; Rare:68 | ||||
| chr16:1992069-1992494 | Common:4; Rare:104 | ||||
| chr16:2009455-2009579 | Rare:30 | ||||
| chr16:2009693-2009992 | Common:15; Rare:128 | ||||
| chr16:2047203-2047309 | Rare:26 | ||||
| chr16:2047680-2048051 | Rare:184; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:2135880-2136125 | Common:1; Rare:119; Clinvar (benign):1 | ||||
| chr16:2153126-2153458 | Common:1; Rare:164 | ||||
| chr16:2155140-2155485 | Common:1; Rare:135 | ||||
| chr16:2155517-2155842 | Common:2; Rare:94 | ||||
| chr16:2205153-2205535 | Common:3; Rare:102 |