Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:45992187-45992397 | Common:1; Rare:72; Clinvar:9; Clinvar (benign):3 | ||||
chr21:45997418-45997761 | Common:5; Rare:116; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
chr21:45998169-45998416 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr21:46116005-46116091 | Rare:19; Clinvar:1 | ||||
chr21:46122474-46122538 | Rare:28; Clinvar:3; Clinvar (benign):2 | ||||
chr21:46125461-46126234 | Common:7; Rare:402; Clinvar:61; Clinvar (benign):35; Clinvar (pathogenic):6 | ||||
chr21:46130038-46130366 | Common:5; Rare:118 | ||||
chr22:18068506-18068603 | Common:2; Rare:14 | ||||
chr22:22298035-22298196 | Common:4; Rare:71 | ||||
chr22:25448023-25448131 | Common:3; Rare:42 | ||||
chr22:28795698-28795835 | Rare:22 | ||||
chr22:29481018-29481108 | Common:1; Rare:38 | ||||
chr22:30922232-30922321 | Rare:38 | ||||
chr22:30969052-30969278 | Common:2; Rare:64 | ||||
chr22:35761204-35761429 | Rare:62 |