| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:56468432-56468710 | Rare:99 | ||||
| chr20:57265834-57266006 | Common:1; Rare:53; Clinvar:1 | ||||
| chr20:57266008-57266454 | Common:1; Rare:104 | ||||
| chr20:57266601-57266904 | Common:2; Rare:84 | ||||
| chr20:57351204-57351287 | Common:2; Rare:24 | ||||
| chr20:57710100-57710210 | Rare:29 | ||||
| chr20:57710508-57710589 | Rare:26 | ||||
| chr20:58388987-58389321 | Common:4; Rare:167; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:58651113-58651345 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:58651604-58651847 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:58652313-58652619 | Common:2; Rare:99 | ||||
| chr20:58839654-58839768 | Rare:26 | ||||
| chr20:58854168-58854328 | Rare:70; Clinvar:2 | ||||
| chr20:58888777-58888820 | Rare:14 | ||||
| chr20:58888821-58889131 | Common:1; Rare:92 |