Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:40687604-40687734 | Rare:26; Clinvar:1; Clinvar (benign):2 | ||||
chr20:40687744-40687845 | Rare:17; Clinvar (benign):1 | ||||
chr20:40688172-40688479 | Rare:97; Clinvar:1 | ||||
chr20:41121697-41122021 | Common:1; Rare:84 | ||||
chr20:41345409-41345576 | Common:1; Rare:17 | ||||
chr20:41349831-41350135 | Common:3; Rare:99 | ||||
chr20:41354459-41354734 | Common:1; Rare:72 | ||||
chr20:45114147-45114336 | Rare:31 | ||||
chr20:45114343-45114657 | Common:1; Rare:58 | ||||
chr20:45338211-45338383 | Common:3; Rare:36 | ||||
chr20:45344323-45344503 | Rare:31 | ||||
chr20:45344549-45344556 | |||||
chr20:47318298-47318365 | Rare:7 | ||||
chr20:47357794-47357908 | Rare:17 | ||||
chr20:47358847-47358953 | Rare:22 |