chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117312532573125327AA--8GENICheterozygous51188773
117312533673125337AT9GENICheterozygous50830178
117312534573125346TTTA9GENICheterozygous51188774
117312545473125455TC15GENIChomozygous50830180
117312555873125559A-15GENIChomozygous50830181
117312600373126004TC18GENIChomozygous50830182
117312667173126672GA12GENIChomozygous50830183
117312801173128012CT10GENICheterozygous51284211
117312826973128270GA13GENICheterozygous51073625
117312846973128470AT11GENICheterozygous51073627
117312866273128663AC20GENIChomozygous50830187
117312866473128665AG21GENIChomozygous50830188
117312873073128731TG21GENICheterozygous51073629
117312876873128769TTG13GENICheterozygous51073631
117312890773128908TC12GENICheterozygous51073632
117312897973128980AG16GENICheterozygous51073634
117312953873129539AG11GENICheterozygous51073636
117312982273129823GA14GENIChomozygous50830189
117312997873129979GA18GENICheterozygous51073638
117312998673129987GA19GENICheterozygous51073640
117313050673130507CT16GENICheterozygous51073644
117313067773130678TA18GENICheterozygous51073646
117313111273131113CT13GENICheterozygous50830190
117313119073131203CAGTTGAGCATTT-------------7GENICheterozygous51073648
117313132873131329GT8GENICheterozygous50830192
117313139273131393TG11GENICheterozygous51073650
117313178473131785CG13GENIChomozygous50830193
117313213673132137TC22GENICpossibly homozygous51073656
117313216273132163TC19GENICheterozygous51073658
117313217773132178GA20GENICpossibly homozygous51073660
117313231073132311CT16GENICheterozygous51073662
117313238773132388GA12GENICheterozygous51073664
117313266573132666CT17GENICheterozygous51073666
117313270173132702GA15GENICheterozygous51073668
117313307273133073CG11GENICheterozygous51073670
117313318273133183CT28GENICheterozygous51073672
117313329773133298CG20GENICheterozygous51073674
117313358273133583TC23GENIChomozygous50830194
117313415373134154TC11GENIChomozygous50830195