Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:38600273-38600572 | Common:4; Rare:72 | ||||
chr2:38751228-38751647 | Common:6; Rare:215 | ||||
chr2:38875619-38876076 | Common:3; Rare:137 | ||||
chr2:39120361-39120510 | Rare:72; Clinvar:2; Clinvar (benign):6 | ||||
chr2:39121021-39121349 | Common:2; Rare:105 | ||||
chr2:39436904-39437476 | Common:5; Rare:216 | ||||
chr2:39665773-39665907 | Rare:32 | ||||
chr2:42169182-42169630 | Common:3; Rare:211 | ||||
chr2:42493968-42494110 | Rare:66 | ||||
chr2:42495013-42495222 | Rare:42 | ||||
chr2:42567912-42568375 | Rare:121 | ||||
chr2:42568414-42568780 | Common:6; Rare:92 | ||||
chr2:42792538-42792704 | Common:2; Rare:48 | ||||
chr2:43225913-43226209 | Common:2; Rare:107 | ||||
chr2:43226314-43226359 | Rare:24 |