| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44531848-44531978 | Common:1; Rare:45 | ||||
| chr20:44651688-44651798 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chr20:44885596-44885838 | Common:4; Rare:82 | ||||
| chr20:44966393-44966566 | Rare:64 | ||||
| chr20:45174676-45174902 | Rare:52 | ||||
| chr20:45362945-45363232 | Rare:89 | ||||
| chr20:45363363-45363487 | Rare:25 | ||||
| chr20:45406541-45406760 | Rare:57 | ||||
| chr20:45415982-45416154 | Rare:44 | ||||
| chr20:45469593-45469859 | Common:1; Rare:85 | ||||
| chr20:45791879-45792005 | Common:1; Rare:49 | ||||
| chr20:45834066-45834216 | Rare:55 | ||||
| chr20:45857343-45857591 | Common:3; Rare:64 | ||||
| chr20:45891250-45891379 | Common:1; Rare:50; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:46089903-46089951 | Rare:20 |