| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:43514731-43514979 | Common:3; Rare:82 | ||||
| chr20:44209985-44210463 | Common:3; Rare:130 | ||||
| chr20:44210610-44211107 | Common:5; Rare:173 | ||||
| chr20:44475748-44475954 | Common:1; Rare:89 | ||||
| chr20:44521832-44522271 | Common:4; Rare:133 | ||||
| chr20:44531775-44531983 | Common:1; Rare:65 | ||||
| chr20:44614601-44615030 | Common:3; Rare:107 | ||||
| chr20:44651618-44651822 | Common:1; Rare:66; Clinvar (benign):1 | ||||
| chr20:44885620-44885883 | Common:4; Rare:86 | ||||
| chr20:45362934-45363224 | Rare:88 | ||||
| chr20:45406161-45406227 | Rare:9 | ||||
| chr20:45406428-45406730 | Rare:78 | ||||
| chr20:45415955-45416283 | Rare:118; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr20:45416389-45416668 | Rare:74; Clinvar (pathogenic):2 | ||||
| chr20:45791852-45792014 | Common:1; Rare:61 |