Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:50192130-50192515 | Common:2; Rare:87 | ||||
chr20:58898912-58899228 | Common:1; Rare:83; Clinvar:2 | ||||
chr20:62942796-62943009 | Rare:47 | ||||
chr20:63865871-63865978 | Common:1; Rare:27 | ||||
chr21:17611530-17611765 | Common:1; Rare:59 | ||||
chr21:26967046-26967186 | Rare:36 | ||||
chr21:26967624-26967888 | Common:2; Rare:72 | ||||
chr21:32765891-32765942 | Common:1; Rare:8 | ||||
chr21:33595795-33596022 | Rare:35 | ||||
chr21:34887980-34888060 | Rare:13 | ||||
chr21:36750239-36750443 | Common:1; Rare:38 | ||||
chr21:37076732-37077037 | Common:3; Rare:62 | ||||
chr21:44962538-44962791 | Common:1; Rare:42 | ||||
chr21:45991732-45992215 | Common:3; Rare:136; Clinvar:10; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr22:20702645-20702833 | Common:2; Rare:39 |