chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3157878364157878365CT25GENIChomozygous60036789
3157878710157878711TTATAC7GENIChomozygous58044011
3157884022157884023TC20GENIChomozygous58044012
3157884612157884613GC29GENIChomozygous57756218
3157887211157887212A-17GENIChomozygous57756226
3157890174157890175T-19GENICheterozygous57756236
3157891250157891252TG--7GENIChomozygous57756240
3157892452157892454CC--14GENIChomozygous57756246
3157893101157893102CT6GENIChomozygous58812045
3157893095157893096TTGTGA7GENICpossibly homozygous58812043
3157888141157888142GGA12GENIChomozygous58564831
3157893103157893104CT5GENIChomozygous58044013
3157893403157893404AG17GENIChomozygous57756250
3157894874157894875CT29GENIChomozygous57756253
3157896379157896380TC18GENIChomozygous57756255
3157899045157899059GTGTGTGTGTGTGT--------------2GENICheterozygous58812049
3157899808157899809AG12GENIChomozygous57756257
3157899044157899045CCGTGTGT2GENICheterozygous58629666
3157905633157905634AG16GENIChomozygous57756259
3157907789157907790AG19GENIChomozygous57756261