chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161854740518547406AG12GENIChomozygous139888990
161854802718548028C13GENICpossibly homozygous139824632
161854861218548613CT20GENIChomozygous139888991
161854921018549211AG22GENIChomozygous139888992
161855011518550116GC24GENIChomozygous139888993
161855034618550347AG23GENIChomozygous139888994
161855053018550531TA23GENIChomozygous139888995
161855090218550903AG14GENIChomozygous139888996
161855114918551150AG29GENIChomozygous139888997
161855186018551861TC23GENIChomozygous139888998
161855282418552825AG19GENIChomozygous139888999
161855299418552995AG26GENIChomozygous139889000
161855314318553144C16GENIChomozygous139824633
161855315618553170TTTTTTTTTTTTTC14GENIChomozygous139824634
161855325818553259TC15GENIChomozygous139889001
161855333318553334AG22GENIChomozygous139889002
161855346018553461TC19GENIChomozygous139889003
161855460218554603TA24GENIChomozygous139889004
161855096218550963CT19GENIChomozygous154993939
161855494118554945AGAG28GENIChomozygous139824635
161855579718555798TC24GENIChomozygous139889005
161855614918556150CG18GENIChomozygous139889006
161855633918556340GA21GENIChomozygous139889007
161855652418556525GA25GENIChomozygous139889008