chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2210079680210079681TC14GENICpossibly homozygous120130465
2210079807210079808AG18GENIChomozygous110222588
2210079915210079916TG25GENIChomozygous110222589
2210081135210081136TC27GENIChomozygous110222590
2210082112210082113AT20GENIChomozygous110222591
2210082957210082958GT8GENIChomozygous110222593
2210083012210083013TA6GENIChomozygous110222594
2210083241210083242TC25GENIChomozygous110222595
2210083488210083489GA10GENIChomozygous120130466
2210083703210083704CG25GENIChomozygous110222596
2210083803210083804CG14GENIChomozygous110222597
2210083834210083835AT20GENIChomozygous110222598
2210083848210083849GA19GENIChomozygous110222599
2210084114210084115CT18GENIChomozygous110222600
2210084278210084279AG15GENIChomozygous110222601
2210084903210084904AG15GENIChomozygous110222602
2210085389210085390CT16GENIChomozygous110222603
2210086943210086944GA40GENIChomozygous110222604
2210087939210087940CT25GENIChomozygous110222605
2210089219210089220CG50GENIChomozygous110222606