| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44475772-44475935 | Rare:74 | ||||
| chr20:44521986-44522243 | Common:2; Rare:79 | ||||
| chr20:44531784-44532176 | Common:3; Rare:114 | ||||
| chr20:44885407-44885842 | Common:7; Rare:131 | ||||
| chr20:44886221-44886438 | Rare:57 | ||||
| chr20:44960370-44960473 | Common:1; Rare:40 | ||||
| chr20:44966386-44966571 | Common:1; Rare:69 | ||||
| chr20:45362896-45363276 | Common:1; Rare:115 | ||||
| chr20:45363290-45363558 | Common:2; Rare:71 | ||||
| chr20:45415999-45416253 | Rare:98; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr20:45791870-45792014 | Common:1; Rare:52 | ||||
| chr20:45834034-45834186 | Rare:53 | ||||
| chr20:45857315-45857639 | Common:3; Rare:94 | ||||
| chr20:45881041-45881258 | Common:2; Rare:52 | ||||
| chr20:45891249-45891379 | Common:1; Rare:50; Clinvar:3; Clinvar (benign):1 |