chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5161242393161242394AG17GENIChomozygous55817793
5161242404161242405TC16GENIChomozygous55817794
5161242407161242408CCCCCCT15GENICpossibly homozygous55817795
5161242415161242416TA18GENIChomozygous55817796
5161242464161242465GA18GENIChomozygous55817797
5161244398161244399T-20GENIChomozygous55817798
5161244508161244509TG27GENICheterozygous55817799
5161244524161244525TG27GENICheterozygous55817800
5161244529161244530GA27GENICheterozygous55817801
5161244532161244533TTA22GENICheterozygous55817802
5161244538161244539GA25GENICheterozygous55817803
5161244798161244799AG16GENIChomozygous55817804
5161244970161244971CT15GENIChomozygous55817805
5161245155161245156TC20GENIChomozygous55817806
5161245201161245202TC16GENIChomozygous55817807
5161245270161245274AAAT----12GENIChomozygous55817808
5161245274161245279AAATC-----12GENICpossibly homozygous55817809
5161245598161245606CTCACGAG--------20GENIChomozygous55817811
5161245635161245636AG28GENIChomozygous55817812
5161246109161246110T-22GENIChomozygous55817813
5161246730161246731AG20GENIChomozygous55817814
5161246785161246795AAAAAAAAAA----------11GENICheterozygous55817815
5161246786161246795AAAAAAAAA---------11GENICheterozygous55817816
5161248844161248845CT15GENIChomozygous55817818
5161248996161248997CT14GENIChomozygous55817819
5161249100161249101AG19GENIChomozygous55817820
5161249268161249269TA6GENIChomozygous55817821
5161249591161249592CT27GENIChomozygous55817822
5161249650161249651CT26GENIChomozygous55817823
5161249695161249696GA18GENIChomozygous55817824
5161249697161249698CT18GENIChomozygous55817825
5161249876161249877GC14GENIChomozygous55817827
5161249906161249907GA12GENICpossibly homozygous55817828
5161249943161249944CT16GENIChomozygous55817829
5161250142161250143GT12GENIChomozygous55817830
5161251163161251164CCA11GENIChomozygous55817831
5161251291161251292AAAAAT5GENIChomozygous55817832
5161251898161251899AG26GENICheterozygous56072228
5161252936161252939GAT---8GENIChomozygous56072229