chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
196810395768103958GGT23GENIChomozygous46301024
196810505868105061CCA---6GENIChomozygous46196039
196810521268105214TA--5GENIChomozygous46196041
196810521368105215AC--5GENIChomozygous46196042
196810521368105214AAC5GENICheterozygous46196043
196810525668105257CT15GENIChomozygous46311470
196810613468106135AATC30GENIChomozygous46196044
196810659868106599CG29GENIChomozygous46301025
196810784468107846TC--12GENICheterozygous46196046
196810799368107995TT--15GENICheterozygous46196047
196810851168108512GT14GENIChomozygous46301026
196810875768108758AG27GENIChomozygous46196049
196811052468110525AG20GENIChomozygous46196056
196811099568110996GA23GENIChomozygous46311472
196811349068113491AG29GENIChomozygous46196063
196811381268113813GA14GENIChomozygous46311474
196811996268119963GA22GENIChomozygous46311478
196812211868122119GC23GENIChomozygous46311480
196812234668122347GGCGTGCTTTTGTTC9GENIChomozygous46196090
196812321468123218ACAC----3GENICheterozygous46311481
196812336968123370GGGAGA2GENIChomozygous46196094
196812437668124380ACAC----2GENIChomozygous46196095
196812536368125364GC29GENIChomozygous46196098
196810799468107995T-15GENICpossibly homozygous46216853
196810974968109750AG20GENICheterozygous46333570