Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:20221585-20221877 | Common:2; Rare:57 | ||||
chr2:20448361-20449124 | Common:5; Rare:198 | ||||
chr2:20540079-20540104 | Rare:8 | ||||
chr2:20593433-20593722 | Common:5; Rare:46 | ||||
chr2:20596458-20596480 | Rare:4 | ||||
chr2:21023293-21023693 | Common:4; Rare:101; Clinvar:5; Clinvar (benign):4 | ||||
chr2:21029637-21030014 | Common:1; Rare:95; Clinvar:2; Clinvar (benign):10 | ||||
chr2:21040566-21040834 | Common:2; Rare:48 | ||||
chr2:21043065-21043129 | Rare:18 | ||||
chr2:21070413-21070555 | Common:2; Rare:30 | ||||
chr2:21096514-21096634 | Rare:18 | ||||
chr2:23198865-23199199 | Common:1; Rare:68 | ||||
chr2:23208507-23208582 | Common:1; Rare:12 | ||||
chr2:25822300-25822378 | Rare:23 | ||||
chr2:26256130-26256252 | Rare:26 |