| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:81077194-81077341 | Common:1; Rare:69 | ||||
| chr16:81779186-81779322 | Rare:57 | ||||
| chr16:82170164-82170314 | Common:3; Rare:83 | ||||
| chr16:84116768-84117078 | Common:4; Rare:126 | ||||
| chr16:84145130-84145284 | Common:1; Rare:80; Clinvar:1 | ||||
| chr16:84504612-84504853 | Common:8; Rare:105 | ||||
| chr16:85027627-85027782 | Common:1; Rare:77 | ||||
| chr16:85799107-85799166 | Rare:20 | ||||
| chr16:85799311-85799800 | Common:3; Rare:149 | ||||
| chr16:86555180-86555306 | Rare:64 | ||||
| chr16:87765911-87766027 | Rare:47 | ||||
| chr16:88570174-88570482 | Common:1; Rare:118 | ||||
| chr16:88650967-88651180 | Common:1; Rare:69; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:88663070-88663362 | Common:7; Rare:119 | ||||
| chr16:88706322-88706556 | Common:5; Rare:115 |