| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:43590612-43590990 | Common:1; Rare:83 | ||||
| chr20:44210726-44211020 | Common:4; Rare:111 | ||||
| chr20:44475818-44475900 | Rare:28 | ||||
| chr20:44521981-44522154 | Common:1; Rare:62 | ||||
| chr20:44885407-44885819 | Common:7; Rare:129 | ||||
| chr20:44966391-44966560 | Rare:63 | ||||
| chr20:45363367-45363501 | Common:1; Rare:28 | ||||
| chr20:45416038-45416153 | Rare:29 | ||||
| chr20:45791890-45792005 | Common:1; Rare:48 | ||||
| chr20:45857343-45857616 | Common:3; Rare:70 | ||||
| chr20:45881013-45881240 | Common:2; Rare:49 | ||||
| chr20:45891250-45891360 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:46364386-46364551 | Rare:63 | ||||
| chr20:46406565-46406787 | Common:2; Rare:60 | ||||
| chr20:47318731-47319027 | Common:1; Rare:93 |