| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69132532-69132671 | Rare:56 | ||||
| chr16:69311102-69311417 | Rare:94 | ||||
| chr16:69339531-69339834 | Common:1; Rare:133; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:69424345-69424686 | Common:1; Rare:89 | ||||
| chr16:69726556-69726802 | Common:3; Rare:56 | ||||
| chr16:69762251-69762379 | Common:1; Rare:35 | ||||
| chr16:70114136-70114376 | Common:3; Rare:84 | ||||
| chr16:70289440-70289767 | Common:3; Rare:135; Clinvar:1 | ||||
| chr16:70346758-70346947 | Common:1; Rare:91 | ||||
| chr16:70523530-70523879 | Common:3; Rare:112; Clinvar (pathogenic):1 | ||||
| chr16:71289292-71289691 | Common:5; Rare:133 | ||||
| chr16:71845780-71846023 | Common:2; Rare:73 | ||||
| chr16:71895254-71895575 | Common:3; Rare:123 | ||||
| chr16:72008532-72008765 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr16:72093579-72093955 | Rare:96 |