| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44885592-44885873 | Common:4; Rare:90 | ||||
| chr20:44966361-44966582 | Common:2; Rare:87 | ||||
| chr20:45363353-45363528 | Common:1; Rare:43 | ||||
| chr20:45406408-45406732 | Rare:87 | ||||
| chr20:45416064-45416201 | Rare:55; Clinvar:1 | ||||
| chr20:45791913-45792005 | Common:1; Rare:37 | ||||
| chr20:45833270-45833450 | Common:1; Rare:27 | ||||
| chr20:45834105-45834229 | Rare:47 | ||||
| chr20:45857293-45857633 | Common:4; Rare:96 | ||||
| chr20:45891206-45891387 | Common:1; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45897505-45898041 | Common:2; Rare:118; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr20:45912078-45912348 | Common:4; Rare:58 | ||||
| chr20:45934536-45934731 | Common:1; Rare:93 | ||||
| chr20:45935045-45935307 | Rare:107 | ||||
| chr20:46021637-46021697 | Common:2; Rare:17 |