chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2264267005264267006TC23GENIChomozygous110441279
2264267132264267133AG17GENIChomozygous110441280
2264267168264267169AC16GENIChomozygous120132767
2264267409264267410CT30GENIChomozygous110441281
2264267517264267518AC19GENIChomozygous110441282
2264267550264267551TC19GENIChomozygous110441283
2264267826264267827CT22GENIChomozygous110441284
2264267972264267973AG17GENIChomozygous120132768
2264268003264268004AG17GENIChomozygous110441285
2264268784264268785CT26GENIChomozygous110441286
2264269097264269098GA13GENIChomozygous110441287
2264269700264269701AG17GENIChomozygous110441288
2264271106264271107TC21GENIChomozygous110441289
2264271201264271202AG22GENIChomozygous110441290
2264271700264271701CT21GENIChomozygous110441291
2264272093264272094CT18GENIChomozygous110441292
2264272097264272098GA17GENIChomozygous110441293
2264272433264272434AG24GENIChomozygous110441294
2264273337264273338CA11GENIChomozygous110441296
2264273349264273350GA11GENIChomozygous110441297
2264273650264273651AC18GENIChomozygous110441298
2264273927264273928TA14GENIChomozygous110441299
2264274250264274251TC20GENIChomozygous110441300
2264274547264274548AT27GENIChomozygous110441301
2264274717264274718TC27GENIChomozygous110441302
2264275033264275034TC8GENIChomozygous110441303
2264275041264275042TA7GENIChomozygous110441304
2264275172264275173CA14GENIChomozygous125613319
2264275558264275559GA4GENIChomozygous125613321
2264272613264272613AC20GENICpossibly homozygous127774012
2264267157264267158A15GENIChomozygous127774008
2264267974264267974A17GENIChomozygous127774009
2264271175264271175T17GENIChomozygous127774011
2264270187264270201CACACACACGCACA12GENICheterozygous131305084
2264270221264270227CGCATG15GENICheterozygous134326604