| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:72100224-72100596 | Common:4; Rare:79 | ||||
| chr16:74296460-74296984 | Common:1; Rare:174 | ||||
| chr16:75250811-75250994 | Common:3; Rare:55 | ||||
| chr16:75305427-75305735 | Rare:51 | ||||
| chr16:75433318-75433606 | Common:3; Rare:115 | ||||
| chr16:75464380-75464484 | Common:2; Rare:51 | ||||
| chr16:75535127-75535491 | Common:3; Rare:66 | ||||
| chr16:75535623-75535870 | Common:1; Rare:62 | ||||
| chr16:75647605-75647829 | Common:2; Rare:110; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190696-77191010 | Common:10; Rare:103 | ||||
| chr16:79599766-79600020 | Common:3; Rare:61; Clinvar (benign):1 | ||||
| chr16:79600055-79600407 | Common:4; Rare:128 | ||||
| chr16:79600618-79600962 | Common:2; Rare:102 | ||||
| chr16:81006324-81006573 | Common:2; Rare:62 | ||||
| chr16:81006798-81007263 | Common:5; Rare:157 |