Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:44425590-44425729 | Rare:57 | ||||
chr21:44801766-44801880 | Rare:49 | ||||
chr21:44873622-44874040 | Common:8; Rare:168 | ||||
chr21:44911949-44912252 | Rare:61 | ||||
chr21:45287879-45288049 | Common:5; Rare:64 | ||||
chr21:45981505-45981813 | Common:23; Rare:70; Clinvar (benign):2 | ||||
chr21:46184423-46184736 | Common:4; Rare:28 | ||||
chr21:46323841-46324215 | Common:3; Rare:133; Clinvar:3; Clinvar (benign):2 | ||||
chr22:17628698-17628840 | Common:1; Rare:47 | ||||
chr22:17638656-17638818 | Rare:56 | ||||
chr22:19432303-19432577 | Common:3; Rare:111 | ||||
chr22:19447690-19447926 | Common:2; Rare:91 | ||||
chr22:19479107-19479457 | Common:4; Rare:130 | ||||
chr22:19479661-19479949 | Common:5; Rare:70 | ||||
chr22:19854809-19854964 | Rare:54 |