chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
29717730297177303CT5GENIChomozygous109937783
29717768297177683TC7GENIChomozygous109937785
29717810397178104TG4GENIChomozygous109937791
29717847197178472CT6GENIChomozygous109937793
29717856097178561CG23GENIChomozygous109937795
29717862597178626GA11GENIChomozygous109937797
29717892197178922CA12GENIChomozygous109937799
29717912097179121CT12GENIChomozygous109937801
29717921897179219CT11GENIChomozygous109937803
29718592297185923GA5GENICheterozygous111328240
29718679497186795TC13GENIChomozygous109937809
29718718797187188AT5GENIChomozygous109937815
29718761097187611AT11GENIChomozygous109937817
29718783897187839GA8GENIChomozygous109937818
29718790997187910GA7GENIChomozygous109937820
29718796297187963CT4GENIChomozygous109937824
29718807197188072GA5GENIChomozygous109937826
29718828197188282CT24GENIChomozygous109937828
29718901997189020GA7GENIChomozygous109937836
29718902597189026CT7GENIChomozygous109937838
29719013297190133GT12GENIChomozygous109937840
29719053797190538CA14GENIChomozygous109937842
29719066497190665TC10GENIChomozygous109937844
29719144997191450AT19GENIChomozygous109937846
29719147597191476GT19GENIChomozygous109937848
29719171897191719TC16GENIChomozygous109937854
29719186897191869CG15GENIChomozygous109937856
29719224997192250GT17GENIChomozygous109937858
29719283297192833CT9GENIChomozygous109937864
29719289297192893TG20GENIChomozygous109937866
29719326497193265AG13GENIChomozygous109937868
29719479897194799GA12GENIChomozygous120125821
29719518697195187TG14GENIChomozygous109937872
29719560197195602AT14GENIChomozygous109937874
29719588297195883GA13GENIChomozygous109937876
29719597797195978CT4GENIChomozygous110958072
29719614897196149TG19GENIChomozygous109937878
29719624297196243AG15GENIChomozygous109937880
29719855397198554CT9GENIChomozygous109937899
29719899497198995CT22GENIChomozygous109937901
29719941197199412AT22GENIChomozygous109937903
29719954997199550TG19GENIChomozygous109937905
29720000397200004CT6GENIChomozygous109937907