chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199089209199089210CT31GENIChomozygous538235397
1199090509199090510T-1GENIChomozygous696768117
1199091225199091226GA21GENIChomozygous538235398
1199093432199093433TC35GENIChomozygous541115911
1199093629199093630AC32GENIChomozygous538235399
1199093873199093874GA16GENIChomozygous538235400
1199093919199093920CCTTTTTT12GENIChomozygous696768118
1199093943199093944CT10GENICheterozygous541115912
1199094029199094030A-23GENIChomozygous696768119
1199094082199094085CTG---31GENIChomozygous696768120
1199094981199094982AG30GENIChomozygous538235401
1199095171199095172GT16GENIChomozygous541115913
1199095810199095811AG22GENIChomozygous538235402
1199095971199095972AAT6GENICheterozygous696768121
1199095972199095973TTTC6GENICheterozygous696768122
1199095973199095974CT8GENICpossibly homozygous541115914
1199096101199096102CT43GENIChomozygous538235403
1199097532199097533GC22GENIChomozygous541115915
1199098345199098346T-15GENIChomozygous696768123
1199099660199099661T-14GENICpossibly homozygous696768124
1199099697199099698TTG14GENIChomozygous696768125