| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:43458516-43458620 | Rare:42 | ||||
| chr20:44180895-44181105 | Rare:33 | ||||
| chr20:44188929-44189091 | Rare:32 | ||||
| chr20:44618085-44618442 | Common:4; Rare:84 | ||||
| chr20:45424253-45424547 | Common:3; Rare:78; Clinvar (pathogenic):1 | ||||
| chr20:45894708-45894869 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:45899611-45899883 | Common:2; Rare:87 | ||||
| chr20:45904820-45905103 | Rare:91 | ||||
| chr20:47318198-47318533 | Rare:61 | ||||
| chr20:47352610-47352650 | Rare:7 | ||||
| chr20:47357794-47357909 | Rare:17 | ||||
| chr20:47641917-47642228 | Common:1; Rare:58 | ||||
| chr20:49094525-49094829 | Rare:52 | ||||
| chr20:49241709-49241987 | Common:1; Rare:69 | ||||
| chr20:49712648-49712839 | Common:2; Rare:54 |