chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1156491943156491944TA29GENICheterozygous60906288
1156491976156491977AT27GENICheterozygous60906289
1156497488156497489CT10GENICheterozygous60906381
1156497499156497500TC11GENICheterozygous60906382
1156497501156497502T-12GENICheterozygous60906383
1156497526156497527GA15GENICheterozygous60906384
1156498378156498379GT19GENICheterozygous60906409
1156497593156497594AG19GENICheterozygous60906385
1156497602156497603CT19GENICheterozygous60906386
1156497628156497629CT19GENICheterozygous60906387
1156498385156498386TC19GENICheterozygous60906410
1156498497156498498CG26GENICheterozygous60906412
1156498515156498516TG33GENICheterozygous60906413
1156498533156498534CT36GENICheterozygous60906414
1156498577156498578AC44GENICheterozygous60906415
1156498583156498584GC43GENICheterozygous60906416
1156498620156498621AT43GENICheterozygous60906417
1156498627156498628GT45GENICheterozygous60906418
1156498647156498648AC41GENICheterozygous60906419
1156498715156498716CT29GENICheterozygous60906420
1156498748156498749TG32GENICheterozygous60906421
1156498761156498762CA38GENICheterozygous60906422