chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108711810987118110TG22GENIChomozygous953090046
108711836487118365AG19GENIChomozygous953090047
108711843087118431AG12GENIChomozygous953090048
108711912187119122CT20GENIChomozygous953090049
108711931787119318AG17GENIChomozygous953090050
108711972587119726CG22GENIChomozygous953090051
108712006987120070AC28GENIChomozygous953090052
108712033387120334CT26GENIChomozygous953090053
108712096087120961CT12GENIChomozygous953090054
108712118587121186CT14GENIChomozygous953090055
108712176187121762AT16GENIChomozygous953090056
108712191187121912TC20GENIChomozygous953090057
108712199887121999CG28GENIChomozygous953090058
108712229387122294GA22GENIChomozygous953090059
108712235487122355TC27GENIChomozygous953090060
108712241387122414GA29GENIChomozygous953090061
108712350687123507TC24GENIChomozygous953090062
108712379987123800AT34GENIChomozygous953090063
108712427187124272GC36GENIChomozygous953090064
108712475387124754AG21GENIChomozygous953090065
108712555187125552GC29GENIChomozygous953090066
108712578087125781CT25GENIChomozygous953090067
108712609387126094CT24GENIChomozygous953090068
108712640387126404CT18GENIChomozygous953090069
108712666287126663TG19GENIChomozygous953090070
108712691187126912TC17GENIChomozygous953090071
108713054887130549CA24GENIChomozygous953090072
108713235087132351AG36GENIChomozygous953090073
108713357387133574GT34GENIChomozygous953090074
108713409587134096AG26GENIChomozygous953090075
108713537187135372AC19GENIChomozygous953090076
108713847987138480TC11GENIChomozygous953090077