| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1773110-1773207 | Rare:29 | ||||
| chr16:1782508-1782939 | Common:4; Rare:138 | ||||
| chr16:1826765-1826948 | Common:2; Rare:56 | ||||
| chr16:1827192-1827501 | Common:2; Rare:163 | ||||
| chr16:1943152-1943515 | Common:1; Rare:116 | ||||
| chr16:1964810-1965066 | Common:6; Rare:114 | ||||
| chr16:1971878-1972153 | Common:3; Rare:80 | ||||
| chr16:2033007-2033352 | Common:1; Rare:85 | ||||
| chr16:2047242-2047432 | Rare:46 | ||||
| chr16:2047770-2048063 | Rare:147; Clinvar:2; Clinvar (benign):7 | ||||
| chr16:2205727-2205885 | Common:3; Rare:70 | ||||
| chr16:2268053-2268186 | Common:1; Rare:69 | ||||
| chr16:2268355-2268520 | Common:2; Rare:57 | ||||
| chr16:2459946-2460133 | Rare:51 | ||||
| chr16:2475008-2475149 | Rare:48 |