chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13100441750100441751CT20GENICpossibly homozygous49867062
13100441799100441800AG5GENICheterozygous50149949
13100441873100441874TA10GENICheterozygous49867064
13100441877100441878CT10GENICpossibly homozygous49867065
13100441897100441898TTGC10GENICheterozygous49867066
13100441907100441911TGTG----5GENICheterozygous49973962
13100441919100441921CA--5GENICheterozygous49867067
13100441940100441941GA14GENICheterozygous49867068
13100441946100441947CG13GENICheterozygous49867069
13100441998100441999GC17GENICheterozygous49973963
13100442018100442019CG16GENICheterozygous49973964
13100442025100442026CT9GENICpossibly homozygous49973965
13100442067100442068AG20GENICheterozygous49973966
13100442069100442070AC22GENICheterozygous50149951
13100442093100442094CG29GENICheterozygous49867074
13100442121100442122CG47GENICheterozygous49867076
13100442126100442128TC--28GENICheterozygous49867077
13100442137100442138CA47GENICheterozygous50149953
13100442142100442144TC--23GENICheterozygous49867078
13100442148100442150TC--24GENICheterozygous49867079
13100442241100442242CCTG50GENICheterozygous49867081
13100442258100442260CC--54GENICheterozygous49867082
13100442379100442380CCTG38GENICheterozygous49867084
13100442514100442516TC--49GENICheterozygous49867085
13100442605100442606GC69GENICheterozygous49973969
13100442642100442643AT10GENIChomozygous49867087
13100442644100442645GT8GENIChomozygous49867088
13100442652100442653AT8GENIChomozygous49867089
13100442654100442655AT8GENIChomozygous49867090
13100442660100442661AT10GENIChomozygous49867091
13100442662100442663AT12GENIChomozygous49867092
13100442670100442671CT13GENIChomozygous49867093
13100442844100442848TGTT----38GENICheterozygous49867094
13100447641100447642CA30GENICheterozygous50149955
13100442159100442160CA56GENICheterozygous50201834