| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1309381-1309755 | Rare:139 | ||||
| chr16:1420714-1420969 | Common:1; Rare:105 | ||||
| chr16:1493258-1493587 | Common:4; Rare:100 | ||||
| chr16:1612037-1612347 | Common:1; Rare:102; Clinvar:1 | ||||
| chr16:1677983-1678321 | Common:3; Rare:111 | ||||
| chr16:1706047-1706304 | Common:2; Rare:80 | ||||
| chr16:1771532-1771865 | Common:3; Rare:130 | ||||
| chr16:1782843-1783009 | Rare:54 | ||||
| chr16:1827161-1827229 | Common:1; Rare:31 | ||||
| chr16:1943222-1943535 | Common:1; Rare:94 | ||||
| chr16:1964824-1965061 | Common:6; Rare:102 | ||||
| chr16:1971878-1972103 | Common:3; Rare:64 | ||||
| chr16:2009589-2009902 | Common:15; Rare:122 | ||||
| chr16:2047795-2048043 | Rare:114; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155482-2155806 | Common:1; Rare:95 |