chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43461506834615069GT17GENIChomozygous663120535
43461522134615222A-20GENIChomozygous764963412
43461708234617083TC23GENIChomozygous663120536
43461781934617820TC36GENIChomozygous663120537
43461803834618039TC20GENIChomozygous663120538
43461831734618318TC21GENIChomozygous663120539
43461871734618718T-30GENIChomozygous764963413
43461913934619140GA12GENIChomozygous663120540
43461947634619477GT20GENIChomozygous663120541
43462030134620302AG26GENIChomozygous663120542
43462032134620322CT27GENIChomozygous663120543
43462048134620482CT23GENIChomozygous663120544
43462055134620552TA23GENIChomozygous663120545
43462070434620705GA28GENIChomozygous663120546
43462070934620710CA29GENIChomozygous663120547
43462073734620738CT30GENIChomozygous663120548
43462114734621148AG23GENIChomozygous663120549
43462115234621155AAA---24GENIChomozygous764963414
43462131434621315GT27GENIChomozygous663120550
43462151934621520GGA17GENIChomozygous764963415
43462184634621848AT--14GENIChomozygous764963418
43462189634621897TC25GENIChomozygous663120551
43462243834622439CT22GENIChomozygous663120552
43462271834622719TTTG18GENIChomozygous764963420
43462276834622769GA20GENIChomozygous663120553
43462291534622916TC28GENIChomozygous663120554
43462301234623016ACAC----4GENIChomozygous764963422
43462308234623083A-25GENIChomozygous764963424
43462309034623091GA26GENIChomozygous663120555
43462356534623566AG28GENIChomozygous663120556
43462403534624036GA20GENIChomozygous663120557
43462423234624233TC25GENIChomozygous663120558