| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44187140-44187367 | Common:1; Rare:47 | ||||
| chr20:44210710-44211140 | Common:5; Rare:155 | ||||
| chr20:44355144-44355466 | Rare:51; Clinvar:2 | ||||
| chr20:44355587-44355755 | Common:1; Rare:28; Clinvar:1 | ||||
| chr20:44400930-44401424 | Common:1; Rare:120; Clinvar:3 | ||||
| chr20:44475772-44475945 | Rare:75 | ||||
| chr20:44521964-44522186 | Common:2; Rare:73 | ||||
| chr20:44531825-44531978 | Common:1; Rare:49 | ||||
| chr20:44651688-44651824 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr20:44885651-44885879 | Common:4; Rare:79 | ||||
| chr20:44966321-44966571 | Common:2; Rare:99 | ||||
| chr20:45174745-45174994 | Common:2; Rare:62; Clinvar:1 | ||||
| chr20:45348337-45348525 | Common:2; Rare:59 | ||||
| chr20:45363108-45363238 | Rare:39 | ||||
| chr20:45363361-45363487 | Rare:26 |