Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:65227593-65227943 | Rare:94 | ||||
chr2:68157450-68157955 | Common:2; Rare:258 | ||||
chr2:68467275-68467606 | Common:1; Rare:84 | ||||
chr2:69829517-69829734 | Rare:87 | ||||
chr2:70087321-70087993 | Common:2; Rare:230 | ||||
chr2:70258198-70258256 | Rare:18 | ||||
chr2:70293657-70293840 | Common:2; Rare:64 | ||||
chr2:71130210-71130680 | Common:6; Rare:135; Clinvar:1; Clinvar (benign):2 | ||||
chr2:73234206-73234361 | Common:2; Rare:46 | ||||
chr2:73284407-73284524 | Rare:26 | ||||
chr2:73828804-73829047 | Common:1; Rare:59 | ||||
chr2:74362650-74363026 | Common:3; Rare:107; Clinvar:5; Clinvar (benign):7 | ||||
chr2:74421618-74421768 | Rare:49 | ||||
chr2:74503314-74503514 | Rare:54 | ||||
chr2:74529629-74530041 | Rare:134; Clinvar:4; Clinvar (benign):1 |