chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13109693186109693187CT23GENICpossibly homozygous49875180
13109710314109710315TTAC19GENICheterozygous49875181
13109714961109714963AG--13GENICheterozygous49875182
13109715418109715419AAG37GENIChomozygous49875183
13109724932109724933CG29GENICheterozygous49875184
13109725009109725010TA38GENICheterozygous49875185
13109725063109725064CA12GENICheterozygous49875186
13109725065109725066TA11GENICheterozygous49875187
13109726725109726727CT--52GENICheterozygous49875188
13109726725109726726C-52GENICheterozygous49875189
13109730423109730424TC107GENICheterozygous49875190
13109730434109730435TC105GENICheterozygous49875191
13109730523109730524CT78GENICheterozygous49875192
13109731088109731089GC77GENICheterozygous49875193
13109735937109735938C-10GENICheterozygous49875194
13109745317109745318T-35GENICheterozygous49875195
13109745322109745323AT37GENICheterozygous49875196
13109745327109745328CA44GENICheterozygous49875197
13109745367109745368AG50GENICheterozygous49875198
13109751827109751828TC50GENIChomozygous49875199
13109761910109761912AA--39GENICheterozygous49875200
13109772199109772200TTC36GENIChomozygous49875201
13109776634109776635T-21GENICheterozygous49875202
13109785967109785968TTGGGAGGAGGA36GENIChomozygous49875203