chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1127826389127826390TG22GENICheterozygous120728729
1127826393127826394TG15GENICheterozygous120728731
1127875459127875460AG13GENIChomozygous108223722
1127932684127932685TC21GENIChomozygous120728733
1127973152127973153CG17GENIChomozygous108223943
1127973230127973231CT11GENIChomozygous108223947
1127976383127976384CA20GENIChomozygous108223959
1127976412127976413CA23GENIChomozygous108223961
1128017461128017462TC15GENIChomozygous108224153
1128019188128019189AT1GENIChomozygous120485685
1128019194128019195AT3GENIChomozygous120485686
1128019546128019547AC19GENIChomozygous120473324
1128024647128024648GT9GENIChomozygous120514783
1128024657128024658GC10GENIChomozygous120514784
1128025965128025966CT29GENIChomozygous108224195
1128041488128041489TG14GENIChomozygous108224254
1128041508128041509CA10GENIChomozygous120473325
1128041509128041510AC9GENIChomozygous108742436
1128065983128065984CA24GENIChomozygous120728735
1128065984128065985GC26GENIChomozygous120514785
1128069138128069139CA19GENIChomozygous120473328
1128069139128069140AT19GENIChomozygous120473329
1128075158128075159GT22GENIChomozygous120473331
1128075173128075174TA19GENIChomozygous108742445
1128075174128075175CT18GENIChomozygous120473332
1128107462128107463AG19GENIChomozygous108224536