chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124073027340730274CT18GENIChomozygous50422955
124073365540733656CT15GENIChomozygous50422956
124073427240734273CT28GENIChomozygous50422957
124073551240735513TC19GENIChomozygous50204502
124073572940735733ATCT----6GENIChomozygous50543746
124073590440735905TC30GENIChomozygous50204503
124073666440736665GA17GENIChomozygous50422959
124073676540736766AG36GENIChomozygous50204505
124073724340737244GT14GENIChomozygous50204506
124073730840737309CCAAAAAA4GENICheterozygous50543747
124073730840737309CCAAAA4GENICheterozygous50422960
124073748840737489CA28GENIChomozygous50422961
124073934640739348TT--11GENICheterozygous50422962
124073934740739348T-11GENICheterozygous50422963
124073954140739542CCTT19GENICpossibly homozygous50204527
124073954140739542CCT19GENICheterozygous50452380
124073985140739852TA30GENIChomozygous50422964
124073996140739962CT29GENIChomozygous50204531
124074034540740346GA21GENIChomozygous50422965
124073338140733382CCAA13GENICpossibly homozygous50323380