Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:44801728-44801876 | Rare:64 | ||||
chr21:44873626-44874050 | Common:8; Rare:170 | ||||
chr21:44939874-44940052 | Common:2; Rare:50 | ||||
chr21:45287879-45288066 | Common:5; Rare:72 | ||||
chr21:46113968-46114028 | Rare:13; Clinvar:1 | ||||
chr21:46184423-46184747 | Common:4; Rare:29 | ||||
chr21:46286233-46286402 | Common:4; Rare:63 | ||||
chr21:46323837-46324224 | Common:3; Rare:142; Clinvar:3; Clinvar (benign):2 | ||||
chr21:46324459-46324712 | Common:4; Rare:98 | ||||
chr21:46348012-46348313 | Rare:65 | ||||
chr21:46458686-46459063 | Common:3; Rare:130 | ||||
chr22:17159165-17159385 | Common:6; Rare:102 | ||||
chr22:17628602-17628860 | Common:2; Rare:80 | ||||
chr22:17638689-17638827 | Rare:50 | ||||
chr22:17774406-17774552 | Rare:54 |