| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:20712543-20713100 | Common:3; Rare:199 | ||||
| chr20:21125789-21126164 | Common:6; Rare:263 | ||||
| chr20:21303220-21303424 | Rare:125 | ||||
| chr20:21303699-21303871 | Rare:69 | ||||
| chr20:22584478-22584878 | Common:8; Rare:199 | ||||
| chr20:23350543-23350886 | Common:2; Rare:196 | ||||
| chr20:23361801-23362253 | Common:10; Rare:296 | ||||
| chr20:23421403-23421673 | Common:5; Rare:113 | ||||
| chr20:23637693-23638483 | Common:20; Rare:272; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr20:24992644-24992896 | Common:11; Rare:192 | ||||
| chr20:25032600-25033010 | Common:2; Rare:135 | ||||
| chr20:25057410-25057820 | Common:7; Rare:172 | ||||
| chr20:25058076-25058241 | Common:2; Rare:36 | ||||
| chr20:25195592-25195855 | Common:7; Rare:152 | ||||
| chr20:25247934-25248399 | Common:3; Rare:245 |