| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45934872-45934983 | Common:1; Rare:41 | ||||
| chr20:45934992-45935426 | Common:2; Rare:184 | ||||
| chr20:45971971-45972655 | Common:4; Rare:227 | ||||
| chr20:46089547-46089764 | Common:3; Rare:85 | ||||
| chr20:46089858-46090113 | Common:1; Rare:86 | ||||
| chr20:46118132-46118353 | Common:3; Rare:80; Clinvar:2; Clinvar (benign):3 | ||||
| chr20:46118605-46118837 | Common:1; Rare:50 | ||||
| chr20:46359169-46359406 | Rare:42 | ||||
| chr20:46363384-46363699 | Rare:46 | ||||
| chr20:46363884-46364123 | Common:1; Rare:52 | ||||
| chr20:46364318-46364597 | Common:2; Rare:99 | ||||
| chr20:46406063-46406402 | Common:3; Rare:91 | ||||
| chr20:46406994-46407146 | Rare:25 | ||||
| chr20:46513508-46513638 | Common:1; Rare:51 | ||||
| chr20:46689068-46689216 | Rare:38; Clinvar (pathogenic):1 |