chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116905115069051151A-11INTERGENIChomozygous50814550
116905642769056428GGT17GENIChomozygous50814588
116906212769062128CCA15GENIChomozygous51217951
116906214869062149CT18GENIChomozygous50814639
116906215369062154GA18GENIChomozygous51069872
116906219669062197TTC15GENIChomozygous50814641
116906227269062273GC15GENIChomozygous50814643
116906233069062331C-17GENIChomozygous50814645
116906235569062356TC15GENIChomozygous50814647
116914064069140641T-11INTERGENICheterozygous50886057
116918438069184381AATG12GENIChomozygous50815474
116921055469210555TC17INTERGENIChomozygous50815637
116921899569218996CCA9INTERGENIChomozygous50815701
116921900669219007TTC9INTERGENIChomozygous50815703
116923669969236700AG16INTERGENICheterozygous51951365