chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2193565485193565486CT17GENIChomozygous110183247
2193566100193566101GC19GENIChomozygous110183248
2193567836193567837GA15GENIChomozygous110183249
2193568437193568438CT16GENIChomozygous110183250
2193569902193569903CT17GENIChomozygous110183251
2193570627193570628TC17GENIChomozygous110183252
2193571702193571703TC16GENIChomozygous110183253
2193571809193571810CG15GENIChomozygous110183254
2193571818193571819AG15GENIChomozygous110183255
2193571853193571854AT12GENIChomozygous110183256
2193571976193571977GC21GENIChomozygous110183257
2193572084193572085GA22GENIChomozygous110183258
2193573080193573081CG367GENICheterozygous110183259
2193573292193573293CG270GENICheterozygous110183260
2193573484193573484C36GENICpossibly homozygous127720743
2193569914193569915T14GENIChomozygous127720741
2193573338193573338G248GENIChomozygous127720742
2193573607193573608C20GENIChomozygous127720747
2193573712193573712T20GENIChomozygous127720748
2193573714193573715CG20GENIChomozygous110616231