| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:39812356-39812464 | Rare:22 | ||||
| chr20:39853497-39853937 | Common:4; Rare:112 | ||||
| chr20:39877750-39878150 | Rare:126 | ||||
| chr20:39986170-39986580 | Common:3; Rare:72 | ||||
| chr20:40502747-40503147 | Common:4; Rare:116 | ||||
| chr20:40687561-40687961 | Rare:112; Clinvar:3; Clinvar (benign):5 | ||||
| chr20:41112124-41112524 | Common:3; Rare:99 | ||||
| chr20:41249223-41249623 | Common:3; Rare:80 | ||||
| chr20:41617539-41617841 | Rare:87 | ||||
| chr20:41692852-41693044 | Common:1; Rare:54 | ||||
| chr20:41693288-41693667 | Common:2; Rare:75 | ||||
| chr20:43657458-43657630 | Common:2; Rare:60 | ||||
| chr20:43761345-43761745 | Rare:131 | ||||
| chr20:43904293-43904490 | Rare:58 | ||||
| chr20:43928449-43928849 | Common:4; Rare:98 |