| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:41028562-41028903 | Rare:126 | ||||
| chr20:41340561-41340842 | Rare:71 | ||||
| chr20:43457805-43457907 | Rare:45 | ||||
| chr20:43590595-43590990 | Common:1; Rare:88 | ||||
| chr20:44187050-44187349 | Common:4; Rare:67 | ||||
| chr20:44187449-44187745 | Common:1; Rare:51 | ||||
| chr20:44210610-44211121 | Common:5; Rare:179 | ||||
| chr20:44311102-44311370 | Common:1; Rare:103 | ||||
| chr20:44475772-44475935 | Rare:74 | ||||
| chr20:44531779-44532012 | Common:1; Rare:71 | ||||
| chr20:44582441-44582665 | Rare:33 | ||||
| chr20:44651688-44651839 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr20:44885441-44885819 | Common:6; Rare:117 | ||||
| chr20:44960370-44960521 | Common:1; Rare:55 | ||||
| chr20:44966370-44966571 | Common:1; Rare:78 |