| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31722481-31722633 | Rare:27 | ||||
| chr20:31722634-31722652 | Rare:4 | ||||
| chr20:31722724-31722962 | Rare:60 | ||||
| chr20:31723481-31723713 | Common:1; Rare:67 | ||||
| chr20:31739093-31739510 | Common:2; Rare:100 | ||||
| chr20:32207191-32207344 | Rare:32 | ||||
| chr20:32207660-32207954 | Common:3; Rare:110 | ||||
| chr20:32358444-32358757 | Common:2; Rare:96; Clinvar:10; Clinvar (benign):2 | ||||
| chr20:33401476-33401589 | Rare:32 | ||||
| chr20:33993073-33993281 | Rare:58 | ||||
| chr20:34112094-34112419 | Rare:105 | ||||
| chr20:34303274-34303391 | Common:1; Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:34516303-34516451 | Common:3; Rare:58 | ||||
| chr20:34558547-34558776 | Common:1; Rare:61 | ||||
| chr20:34677078-34677329 | Rare:66 |