chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124073027340730274CT28GENIChomozygous50422955
124073338140733382CCA7GENICheterozygous50204499
124073365540733656CT5GENIChomozygous50422956
124073427240734273CT36GENIChomozygous50422957
124073551240735513TC14GENIChomozygous50204502
124073572940735733ATCT----9GENICheterozygous50543746
124073590440735905TC34GENIChomozygous50204503
124073338140733382CCAA7GENICheterozygous50323380
124073570440735705CCATCT9GENICheterozygous50323382
124073666440736665GA24GENIChomozygous50422959
124073676540736766AG26GENIChomozygous50204505
124073724340737244GT18GENIChomozygous50204506
124073730840737309CCAAAA2GENIChomozygous50422960
124073748840737489CA21GENIChomozygous50422961
124073934740739348T-2GENICheterozygous50422963
124073954140739542CCTT11GENIChomozygous50204527
124073985140739852TA41GENIChomozygous50422964
124073996140739962CT26GENIChomozygous50204531
124074034540740346GA34GENIChomozygous50422965