chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124760989847609899AG9GENIChomozygous50486922
124761018147610182CT24GENIChomozygous50486926
124761052147610522AT16GENIChomozygous50486928
124761058047610581GT20GENIChomozygous50486930
124761152847611529CCCATACATACATACATA9GENIChomozygous50546012
124761206847612069GA21GENIChomozygous50486932
124761212447612125GA20GENIChomozygous50486934
124761212647612127CT19GENIChomozygous50486937
124761253147612532CA31GENIChomozygous50486939
124761266747612668G-16GENIChomozygous50486941
124761275247612753TC23GENIChomozygous50486943
124761278047612790ACACACACAC----------14GENICheterozygous50546014
124761278247612790ACACACAC--------14GENICpossibly homozygous50622651
124761280847612809AT18GENICpossibly homozygous50622652
124761287547612876GA29GENIChomozygous50486949
124761295247612953AG23GENIChomozygous50486951
124761315147613152CT24GENIChomozygous50486953
124761348247613483TC19GENIChomozygous50486955
124761391947613920TA15GENIChomozygous50486957
124761392647613927GA17GENIChomozygous50486959
124761393047613931AG14GENIChomozygous50486961
124761393947613940AT14GENIChomozygous50486963
124761394947613950TA17GENIChomozygous50486965
124761431047614311GA22GENICpossibly homozygous50486967
124761438947614390AAGTGTGTGTGAGTGT26GENIChomozygous50546015
124761444447614445AG19GENIChomozygous50486971
124761459647614597AG14GENIChomozygous50486973
124761522947615230CT25GENIChomozygous50486975
124761589947615903CTCT----9GENICheterozygous50223081
124761590147615903CT--9GENICheterozygous50223083
124761596147615975CACACACACACACA--------------4GENIChomozygous50546016
124761604847616049GA6GENIChomozygous50486977
124761826847618276GGTGAGCA--------5GENICheterozygous50223089
124761911447619115AAGATG7GENIChomozygous50455706
124762074347620744GGACACACACAC5GENIChomozygous50546018
124762138847621389AACAAACCAGGGTCTCCTGGCCAGGGAATGGTCTGGCCCATGG11GENIChomozygous50546020
124762139047621391TTCAAATCTGCCTTCCCATG11GENIChomozygous50546021
124762206547622066GC11GENIChomozygous50486979
124762504047625041TC23GENICpossibly homozygous50486981
124762613747626138TG8GENIChomozygous50486985
124762654647626547G-9GENIChomozygous50223093
124762691647626917AC12GENIChomozygous50486987
124762709047627091AG16GENIChomozygous50546022
124762709147627092GA15GENIChomozygous50546023
124762714347627144AG15GENIChomozygous50486989
124762735447627355CT6GENIChomozygous50486992
124762762047627621GA20GENIChomozygous50486994
124762763247627633CG24GENIChomozygous50486996
124762792447627925CT15GENIChomozygous50486998
124762810647628111TATAT-----8GENIChomozygous50546024
124762811747628118CT8GENIChomozygous50487000
124762825047628251AG9GENIChomozygous50487002
124762885647628857CT4GENIChomozygous50487004
124762903547629036AAT4GENIChomozygous50487006
124762903647629037CT4GENIChomozygous50546025
124763020947630210TTG3GENICheterozygous50487008
124763028447630285GA13GENIChomozygous50487010
124763071947630720CT12GENIChomozygous50487012
124763106347631064CT10GENIChomozygous50487014
124763177047631772TT--10GENIChomozygous50487016
124763193647631937TTGGG2GENICheterozygous50487018
124763313447633135TC16GENIChomozygous50487020
124763410147634102T-13GENICpossibly homozygous50343202