chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103903971339039714G19GENIChomozygous138679685
103903986739039868GA19GENIChomozygous145736993
103906002239060023GT7GENIChomozygous403283297
103904038439040385GA14GENIChomozygous154627301
103905727139057272GC12GENICheterozygous154628885
103905727339057274GC12GENICheterozygous154628886
103904040739040408GA16GENIChomozygous138770206
103904612639046127TC27GENIChomozygous138770209
103905227839052279GC25GENIChomozygous138770213
103904038439040385G14GENICheterozygous403283294
103906002239060023G7GENICheterozygous403283296
103905727139057272G12GENIChomozygous403774058
103905727339057274G12GENIChomozygous403938131
103906002639060027G6GENICheterozygous403283300
103906002639060027GT6GENIChomozygous403283301
103906199039061991AG21GENIChomozygous138770218
103906255939062560CT30GENIChomozygous145736994
103906311639063117CA29GENIChomozygous138770220
103906315339063153CTGC27GENIChomozygous138679690
103906472039064721CT18GENIChomozygous145736995
103906745539067456AC23GENIChomozygous145736996
103906983339069834TC24GENIChomozygous142234992
103907065739070658AC23GENIChomozygous154628894
103907065739070658AT23GENICheterozygous154628895
103907078039070781GA28GENICpossibly homozygous145736997
103907115639071157GA30GENIChomozygous145736998
103907147039071471TA23GENIChomozygous142234994
103907309439073095CT30GENIChomozygous142234996
103907422439074225GA27GENIChomozygous145736999
103907626239076263CA9GENIChomozygous145737000
103907629539076295G13GENIChomozygous145728555
103907387239073900CCCATGCCTGGGATCTTTGGGGGGCTTA13GENIChomozygous145728554
103906595739065958AG33GENIChomozygous138770221
103907729739077298AG26GENIChomozygous138770224
103907765639077657CG36GENIChomozygous145737001
103907810839078109AG21GENIChomozygous138770226
103907960739079608GA26GENIChomozygous138770229
103908053139080532CT16GENIChomozygous145737002
103908120239081203TC19GENIChomozygous138770230
103908120539081206AT19GENIChomozygous138770231
103908286139082862CA20GENIChomozygous145737003