chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37409962074099621CCT8GENICpossibly homozygous58374293
37409962174099622T-8GENICheterozygous58157117
37410014174100142CCTGTGTG8GENIChomozygous58688199
37410469574104696CCA10GENIChomozygous57453460
37410539674105397GA23GENIChomozygous57453470
37410618074106181AG22GENIChomozygous57453478
37410627674106277TC22GENIChomozygous57898853
37410699674106997CA13GENIChomozygous57453482
37410755174107552GA17GENIChomozygous57453484
37410882774108828CCTTCCTT18GENIChomozygous57453490
37411327874113279TC15GENIChomozygous57453530
37411377074113771A-9GENIChomozygous58292042
37411829774118298CCTT13GENICpossibly homozygous58596050
37411837874118379TC27GENIChomozygous57453573
37411845274118453GA16GENICheterozygous57453579
37412065974120660CT20GENIChomozygous57453601
37411848674118487TC26GENIChomozygous58421915
37412100674121007CG24GENIChomozygous58421916
37411848974118490CT34GENICheterozygous58550628
37412741374127414CT15GENIChomozygous58421918
37413180574131806CT14GENIChomozygous58421919
37413300174133002GGT15GENIChomozygous58292044
37413553874135539CT19GENIChomozygous58421920
37413655174136552AG19GENIChomozygous57453653
37413744374137444CA30GENIChomozygous57453655
37413757674137579TTG---25GENIChomozygous57453661
37413809474138095CA24GENIChomozygous57453665