chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2551615525516156CT10GENIChomozygous62926710
X2553636825536369AT13GENIChomozygous63032800
X2551906225519063CT17GENIChomozygous63032796
X2552084125520842TG7GENIChomozygous63032797
X2553546825535469TC10GENIChomozygous63032798
X2553550325535504TC9GENIChomozygous63032799
X2553708925537090GA10GENICpossibly homozygous63032801
X2553846225538463TA9GENIChomozygous63032803
X2553911125539112TC11GENIChomozygous62926727
X2553917925539180TC16GENIChomozygous62926728
X2553964325539644GA12GENIChomozygous63032804
X2553998325539984AG7GENIChomozygous62926730
X2554060925540610GA18GENIChomozygous63032805
X2554251025542511TC7GENIChomozygous62926732
X2554255725542558CT5GENIChomozygous63032806
X2554261525542616CG5GENIChomozygous63032807
X2554284125542842GT7GENIChomozygous62926733
X2554352725543528GA16GENIChomozygous63032808
X2554421225544213TC8GENIChomozygous63032809
X2554430325544304TC12GENIChomozygous63032810
X2554447825544479AT9GENIChomozygous62926735
X2554470725544708AG1GENIChomozygous63032811
X2554482725544828CT6GENIChomozygous63032812
X2554637125546372TC7GENIChomozygous62926738
X2554674825546749CT2GENIChomozygous62926739