| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:240256044-240256159 | Rare:26 | ||||
| chr2:241166973-241167144 | Rare:55 | ||||
| chr2:241684863-241684907 | Rare:15 | ||||
| chr2:242088553-242088733 | Rare:71 | ||||
| chr20:327060-327455 | Common:4; Rare:118 | ||||
| chr20:419409-419750 | Common:1; Rare:112; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr20:419822-419989 | Common:9; Rare:38 | ||||
| chr20:420059-420401 | Common:2; Rare:64 | ||||
| chr20:421167-421279 | Common:1; Rare:35 | ||||
| chr20:489780-490016 | Common:1; Rare:39 | ||||
| chr20:842384-842672 | Common:2; Rare:55 | ||||
| chr20:1352146-1352417 | Common:34; Rare:83 | ||||
| chr20:1418266-1418483 | Rare:31 | ||||
| chr20:1809773-1810022 | Common:1; Rare:40 | ||||
| chr20:1861821-1861953 | Rare:27 |