chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84817058048170581GA29GENIChomozygous52623020
84817209348172094TA19GENIChomozygous52623022
84817254048172541AAG26GENIChomozygous52623024
84817258548172586GA30GENIChomozygous52623026
84817313348173134CT15GENIChomozygous52623028
84817330948173310CT14GENIChomozygous52623032
84817382248173823CT16GENIChomozygous52623034
84817383948173840AAC10GENIChomozygous52623036
84817384248173848TGAGGT------14GENIChomozygous52623037
84817397848173979CCACA26GENIChomozygous52623039
84817422748174229TT--23GENIChomozygous52623041
84817476148174762GA33GENIChomozygous52623043
84817534248175343GGCT32GENIChomozygous52623045
84817546548175466TC35GENIChomozygous52623047
84817548948175490AAC28GENIChomozygous52623049
84817562848175629TG25GENIChomozygous52623051
84817563648175637CT23GENIChomozygous52623053
84817569548175696TTACACAC2GENICheterozygous53383023
84817677748176778TG30GENIChomozygous52623055
84817725448177255CT21GENIChomozygous52623057
84817766148177662TTATTCATTCATTC7GENIChomozygous53383031
84817800148178002GC23GENIChomozygous52623062
84817801048178011GA24GENIChomozygous52623064
84817819248178193GGC17GENIChomozygous52623066
84817840548178409GGGA----13GENIChomozygous52623068
84817907748179078GA19GENIChomozygous52623076
84817913948179157GTGTGCGCGCGCGCGCGC------------------7GENICpossibly homozygous52623078
84817921548179216CT29GENIChomozygous52623082
84817927448179275TC27GENIChomozygous52623084
84817934048179341TC20GENIChomozygous52623086
84817934348179344GC21GENIChomozygous52623088
84817944048179441AG25GENIChomozygous52623090
84817964148179642TC23GENIChomozygous52623092
84817969248179693CT19GENIChomozygous52623094
84818017148180172AC25GENICpossibly homozygous52623096
84818041048180411TC22GENIChomozygous52623098
84818136948181370TTG22GENIChomozygous52623100
84818247848182479A-29GENIChomozygous52623102