| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89560411-89560791 | Common:1; Rare:172 | ||||
| chr16:89575072-89575313 | Common:2; Rare:61 | ||||
| chr16:89575415-89575848 | Common:5; Rare:142 | ||||
| chr16:89657628-89658163 | Common:4; Rare:262 | ||||
| chr16:89686666-89686763 | Common:5; Rare:63 | ||||
| chr16:89686813-89687067 | Common:4; Rare:114 | ||||
| chr16:89687278-89687517 | Rare:67 | ||||
| chr16:89701599-89701827 | Common:1; Rare:79 | ||||
| chr16:89701984-89702283 | Common:9; Rare:97 | ||||
| chr16:89712484-89712593 | Common:3; Rare:55 | ||||
| chr16:89720827-89721065 | Common:1; Rare:73 | ||||
| chr16:89721394-89721592 | Common:3; Rare:98 | ||||
| chr16:89721935-89722305 | Common:1; Rare:112 | ||||
| chr16:89764484-89764762 | Rare:80 | ||||
| chr16:89764909-89765249 | Common:4; Rare:149; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):5 |