chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17897221078972210CTCT14GENIChomozygous142788280
17897529478975295AC16GENIChomozygous142833113
17897827678978277TG10GENIChomozygous142833114
17898366678983667AG25GENIChomozygous142833115
17898608278986094GAGAGAGAGAGC6GENIChomozygous142788281
17898752678987527GA17GENIChomozygous142833116
17898839078988391CT21GENIChomozygous142833117
17898868178988681C18GENIChomozygous142788282
17898056078980561T19GENIChomozygous140957742
17898704978987050GC11GENIChomozygous153865487
17898704978987050G11GENICheterozygous404051259
17899183578991836GA27GENIChomozygous142833118
17899313578993136GA23GENIChomozygous142833119
17899558678995587AG20GENIChomozygous142833120
17899574478995744A27GENIChomozygous142788283
17899708778997088GA32GENIChomozygous142833121
17899872678998727TA16GENIChomozygous142833122
17900294279002946AGAG20GENIChomozygous142788284
17900611179006112CT20GENIChomozygous142833128
17899941678999417GA29GENIChomozygous142833123
17900129979001300CG5GENIChomozygous142833124
17900269579002696AG21GENIChomozygous142833125
17900466879004669GA17GENIChomozygous142833126
17900483279004833AG23GENIChomozygous142833127
17899163078991631G3GENIChomozygous149483706
17900643979006440AC25GENIChomozygous142833129