chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167394944073949441GA16GENIChomozygous64951473
167395035073950351GA21GENIChomozygous64951475
167395345973953460CT19GENICheterozygous64584796
167395462973954630AG22GENIChomozygous64951479
167395467873954679TC19GENIChomozygous64951481
167395540173955402GA13GENIChomozygous64951483
167395541973955420TC17GENIChomozygous64951485
167395558073955581AG29GENIChomozygous64584805
167395581873955819AG18GENIChomozygous64951487
167395604273956043CT36GENIChomozygous64951489
167395619273956193CT22GENIChomozygous64951491
167395637873956379GA19GENICpossibly homozygous64951493
167395668973956690AG30GENIChomozygous64951495
167395805973958060TC19GENIChomozygous64951497
167395874873958749AG12GENIChomozygous64584811
167396075173960752AG19GENIChomozygous64951499
167396371873963719AG21GENIChomozygous64584822
167396553973965540AG3GENIChomozygous64774590
167396799273967993CT21GENIChomozygous64951501
167396859973968600CT16GENIChomozygous64951503
167396872873968729CA14GENIChomozygous64951505
167396890173968902AG11GENIChomozygous64584840
167416876374168764CT21GENIChomozygous64951507
167416909174169092CT25GENIChomozygous64951509
167416943374169434AG21GENIChomozygous64951511
167416955674169557CG23GENIChomozygous64951513
167416971874169719TG15GENIChomozygous64584860
167417008974170090GC14GENIChomozygous64951515
167417053074170531AC9GENIChomozygous64584863
167417120974171210AG18GENIChomozygous64584867
167417146474171465TC21GENIChomozygous64951517
167417155774171558TA15GENIChomozygous64584869
167417258774172588CT24GENIChomozygous64951519
167417272374172724TG12GENIChomozygous64584872
167417310074173101TA18GENIChomozygous64584875
167417415674174157CT10GENICpossibly homozygous64584881