chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17897221078972210CTCT25GENIChomozygous142788280
17897529478975295AC41GENIChomozygous142833113
17897827678978277TG8GENIChomozygous142833114
17898366678983667AG22GENIChomozygous142833115
17898704978987050GC17GENICheterozygous153865487
17898558278985583A8GENICheterozygous404769390
17898558478985585A7GENICheterozygous404769391
17898558678985587A6GENICheterozygous404797607
17897856278978563CG22GENIChomozygous147925749
17898558678985587AC6GENICheterozygous147925750
17898056078980561T28GENICpossibly homozygous140957742
17898558278985583AC8GENICheterozygous143785247
17898558478985585AC7GENICheterozygous143785248
17898704878987050TG17GENICheterozygous143739796
17898704978987050G17GENICheterozygous404051259
17898752678987527GA25GENIChomozygous142833116
17898839078988391CT37GENIChomozygous142833117
17898868178988681C36GENIChomozygous142788282
17899191878991919GA28GENIChomozygous147925751
17899207278992073AG16GENICheterozygous404051260
17899207278992073A16GENIChomozygous404051261
17899313578993136GA35GENIChomozygous142833119
17899558678995587AG19GENIChomozygous142833120
17899574478995744A25GENIChomozygous142788283
17899708778997088GA37GENIChomozygous142833121
17899872678998727TA25GENIChomozygous142833122
17899941678999417GA38GENIChomozygous142833123
17900269579002696AG39GENIChomozygous142833125
17900294279002946AGAG32GENIChomozygous142788284
17900466879004669GA25GENIChomozygous142833126
17900483279004833AG33GENIChomozygous142833127
17900611179006112CT25GENIChomozygous142833128
17900643979006440AC41GENIChomozygous142833129
17899062778990628TC3GENICheterozygous135576895
17900127879001281GGT10GENICheterozygous144228391