chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124073027340730274CT12GENIChomozygous50422955
124073338140733382CCA12GENICheterozygous50204499
124073365540733656CT6GENIChomozygous50422956
124073427240734273CT20GENIChomozygous50422957
124073494440734946AA--8GENICheterozygous50204501
124073551240735513TC9GENIChomozygous50204502
124073572940735733ATCT----11GENIChomozygous50543746
124073590440735905TC14GENIChomozygous50204503
124073666440736665GA13GENIChomozygous50422959
124073676540736766AG21GENIChomozygous50204505
124073724340737244GT10GENIChomozygous50204506
124073730840737309CCAAAAAA7GENICheterozygous50543747
124073730840737309CCAAAA7GENICheterozygous50422960
124073748840737489CA13GENIChomozygous50422961
124073931440739315G-5GENICheterozygous50204524
124073934740739348T-1GENIChomozygous50422963
124073954140739542CCTT4GENIChomozygous50204527
124073985140739852TA16GENIChomozygous50422964
124073996140739962CT11GENIChomozygous50204531
124074034540740346GA19GENIChomozygous50422965
124073338140733382CCAA12GENICheterozygous50323380