chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2104934539104934540T9GENIChomozygous127660577
2104934554104934554C10GENIChomozygous127660578
2104934616104934616G12GENIChomozygous127660579
2104934625104934626G14GENIChomozygous127660580
2104934652104934653T15GENIChomozygous127660581
2104934724104934725A9GENIChomozygous127660582
2104934741104934741C6GENIChomozygous127660583
2104934744104934745T6GENIChomozygous127660584
2104937912104937913CA19GENIChomozygous109961631
2104937951104937952CG27GENIChomozygous109961633
2104937968104937969C27GENIChomozygous127660595
2104937984104937985CG26GENIChomozygous109961635
2104937995104937996CA26GENIChomozygous109961637
2104937997104937998CG28GENIChomozygous109961639
2104938010104938011TG30GENIChomozygous110580165
2104938012104938013CT28GENIChomozygous109961641