chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141763972417639725TC17GENIChomozygous986200173
141764052517640526TC16GENIChomozygous986200174
141764261817642619CT21GENIChomozygous986200175
141764265617642657CA24GENIChomozygous986200176
141764342217643423GC22GENIChomozygous986200177
141764352417643525CT20GENIChomozygous986200178
141764359417643595CA11GENIChomozygous986200179
141764416617644167GT29GENIChomozygous986200180
141764622417646225CT21GENIChomozygous986200181
141764869017648691GC19GENIChomozygous986200182
141764987017649871CA20GENIChomozygous986200183
141765004317650044CT20GENIChomozygous986200184
141765048617650487CT24GENIChomozygous986200185
141765072117650722AG13GENIChomozygous986200186
141765073017650731CT13GENIChomozygous986200187
141765115717651158AT12GENIChomozygous986200188
141765116317651164GA14GENIChomozygous986200189
141765141217651413AT15GENIChomozygous986200190
141765144717651448TG14GENIChomozygous986200191
141765161617651617AG24GENIChomozygous986200192
141765171117651712GC12GENIChomozygous986200193
141765171817651719GA8GENIChomozygous986200194
141765172617651727GT7GENIChomozygous986200195
141765179617651797GA12GENIChomozygous986200196
141765416017654161GA22GENIChomozygous986200197
141765416217654163AG23GENIChomozygous986200198
141765581617655817TC34GENIChomozygous986200199
141765645617656457TC18GENIChomozygous986200200
141765649817656499CT14GENIChomozygous986200201
141765685017656851AG23GENIChomozygous986200202