Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:677364-677557 | Common:1; Rare:80 | ||||
chr2:3377796-3378035 | Common:2; Rare:66 | ||||
chr2:3558228-3558673 | Common:6; Rare:171 | ||||
chr2:3575107-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
chr2:9423443-9423682 | Rare:76 | ||||
chr2:9555717-9555966 | Common:2; Rare:85 | ||||
chr2:9843250-9843539 | Common:6; Rare:86 | ||||
chr2:10689892-10690004 | Common:2; Rare:44 | ||||
chr2:12716629-12716933 | Common:3; Rare:89 | ||||
chr2:15561309-15561421 | Rare:43 | ||||
chr2:17753706-17754174 | Common:4; Rare:145; Clinvar (benign):1 | ||||
chr2:19990046-19990211 | Rare:45 | ||||
chr2:20350340-20350462 | Rare:44 | ||||
chr2:21123839-21124007 | Common:1; Rare:53 | ||||
chr2:23940412-23940514 | Common:3; Rare:39 |