chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5120504474120504475TC17GENICheterozygous55671350
5120506134120506135TC20GENICheterozygous55671352
5120506172120506173GA15GENICheterozygous55671354
5120508265120508266CT23GENICheterozygous55671370
5120510050120510051TC28GENICheterozygous55671380
5120513599120513600TC23GENICheterozygous55671410
5120518421120518422CA31GENICheterozygous55671438
5120518460120518461TC43GENICheterozygous55671440
5120518545120518546TC31GENICheterozygous55671442
5120518618120518619AAAT12GENICheterozygous58208504
5120518620120518621AT11GENICheterozygous58208507
5120527424120527425AG9GENICheterozygous55671494
5120530080120530081AG14GENICheterozygous55671500
5120533952120533953AT21GENICheterozygous55671510
5120534517120534518CT81GENICheterozygous55671525
5120536885120536886CT19GENICheterozygous55671541
5120551848120551849GA28GENICheterozygous55671598
5120557511120557512AG31GENICheterozygous55671647
5120557709120557710CG39GENICheterozygous55671649
5120557797120557798CT17GENICheterozygous55671651
5120562272120562273TC21GENICheterozygous55671700
5120572608120572609GC9GENICheterozygous55671821
5120583279120583280TC11GENICheterozygous55671869
5120586399120586400TC26GENICheterozygous55671887
5120586994120586995GA33GENICheterozygous55671889
5120591141120591142T-73GENICheterozygous55671899
5120596940120596941CA11GENICheterozygous55671921
5120605291120605292TC16GENICheterozygous55671963
5120613507120613508CA27GENICheterozygous55672006
5120613598120613599GGT51GENICheterozygous55672008
5120614768120614769CT7GENICheterozygous55672014
5120623974120623975GA16GENICheterozygous55672052
5120624349120624350TC33GENICheterozygous55672058
5120634049120634050AG49GENICheterozygous55672100
5120634112120634113GA42GENICheterozygous55672102
5120643390120643391G-39GENICheterozygous55672174
5120646740120646741TC51GENICheterozygous55672186
5120647644120647645C-46GENICheterozygous55672190
5120647743120647744GA16GENICheterozygous55672192
5120677488120677489GA16GENICheterozygous55672281