chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13109683134109683135GT39GENICheterozygous50449308
13109693186109693187CT21GENICpossibly homozygous49875180
13109700532109700533CG43GENICheterozygous50449310
13109708316109708317TTCA9GENICheterozygous49987998
13109715418109715419AAG35GENIChomozygous49875183
13109724844109724846TT--14GENICheterozygous49988024
13109724899109724900TC17GENICheterozygous49988025
13109724907109724908TG19GENICheterozygous49988026
13109724932109724933CG25GENICheterozygous49875184
13109725009109725010TA18GENICheterozygous49875185
13109725044109725045AT15GENICheterozygous50157505
13109725054109725055TA13GENICheterozygous49988027
13109725063109725064CA13GENICheterozygous49875186
13109725065109725066TA13GENICheterozygous49875187
13109726725109726727CT--69GENICheterozygous49875188
13109726725109726726C-69GENICheterozygous49875189
13109726783109726784GA246GENICheterozygous49988031
13109730423109730424TC148GENICheterozygous49875190
13109730434109730435TC134GENICheterozygous49875191
13109730523109730524CT97GENICheterozygous49875192
13109733120109733126AACAAC------16GENICheterozygous49988040
13109733123109733126AAC---16GENICpossibly homozygous50449312
13109745317109745318T-52GENICheterozygous49875195
13109745322109745323AT57GENICheterozygous49875196
13109745327109745328CA65GENICheterozygous49875197
13109745367109745368AG79GENICheterozygous49875198
13109751020109751021A-32GENICheterozygous49988092
13109751827109751828TC47GENICpossibly homozygous49875199
13109761870109761874ACAC----24GENICheterozygous49988138
13109772199109772200TTC29GENIChomozygous49875201
13109779534109779535CT112GENICheterozygous50449314
13109785967109785968TTGGGAGGAGGA19GENIChomozygous49875203