chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101657006716570068TTAC4GENIChomozygous754776567
101657514416575145TC27GENIChomozygous646115016
101657532216575331GTCCTTCCA---------18GENIChomozygous754776568
101657540116575402AATT8GENICpossibly homozygous754776569
101657540116575402AATCTTT8GENICheterozygous754776570
101657561316575614AC20GENIChomozygous646115017
101657571616575717TTA13GENIChomozygous754776571
101657587316575874AG16GENIChomozygous646115018
101657591016575911CT17GENIChomozygous646115019
101657602716576028A-12GENIChomozygous754776572
101657653716576538GGT18GENIChomozygous754776573