| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70454331-70454629 | Common:2; Rare:79 | ||||
| chr16:70523451-70523899 | Common:3; Rare:161; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71809025-71809326 | Common:3; Rare:96 | ||||
| chr16:71883967-71884078 | Rare:35 | ||||
| chr16:71894288-71894435 | Rare:47 | ||||
| chr16:71894761-71895104 | Common:3; Rare:104 | ||||
| chr16:71895280-71895566 | Common:2; Rare:111 | ||||
| chr16:72008531-72008804 | Common:5; Rare:99; Clinvar (benign):2 | ||||
| chr16:72093494-72093950 | Rare:116 | ||||
| chr16:72094372-72094503 | Common:1; Rare:23 | ||||
| chr16:73059075-73059219 | Rare:22 | ||||
| chr16:74296491-74296974 | Common:1; Rare:167 | ||||
| chr16:74304172-74304398 | Common:2; Rare:48 | ||||
| chr16:74607011-74607192 | Rare:100 | ||||
| chr16:74666833-74667098 | Common:4; Rare:96 |