Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:23633591-23633709 | Common:2; Rare:27 | ||||
chr20:25751093-25751192 | Rare:16 | ||||
chr20:35548510-35548864 | Rare:110 | ||||
chr20:36050538-36050644 | Common:1; Rare:44 | ||||
chr20:45894708-45894869 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr20:47357800-47357840 | Rare:8 | ||||
chr20:53592735-53592768 | Rare:8 | ||||
chr21:28090201-28090423 | Common:4; Rare:51 | ||||
chr21:45989614-45989778 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):1 | ||||
chr21:45990815-45991029 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
chr21:45992017-45992182 | Common:1; Rare:60; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr21:46122156-46122178 | Rare:5; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr22:22297822-22298209 | Common:13; Rare:144 | ||||
chr22:25447978-25448164 | Common:4; Rare:67 | ||||
chr22:27224537-27224772 | Common:4; Rare:49 |