chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1143686807143686808A-12GENICheterozygous61903022
1143688087143688088TC31GENIChomozygous60878274
1143690280143690281C-6GENICheterozygous62444897
1143690702143690703TA18GENICpossibly homozygous60878283
1143690823143690824GA12GENIChomozygous61903024
1143691396143691397GT17GENIChomozygous61903025
1143692711143692712CT16GENICpossibly homozygous60878286
1143693724143693725GC15GENICheterozygous60878287
1143694924143694925A-9GENIChomozygous61532315
1143695310143695311GA20GENICpossibly homozygous61903027
1143695431143695432AT18GENIChomozygous60878295
1143698329143698330GA3GENICheterozygous61903029
1143698414143698415GC9GENICpossibly homozygous60878299
1143698704143698705AG13GENICpossibly homozygous60878300
1143700534143700535AG9GENIChomozygous61903031
1143700825143700826GA19GENICheterozygous61903032
1143701108143701109TC15GENICpossibly homozygous60878305
1143701429143701430GA23GENIChomozygous61903033
1143701501143701502GA30GENICpossibly homozygous60878307
1143701609143701610AG9GENIChomozygous60878308
1143701674143701675CCTT2GENIChomozygous60878309
1143701695143701699AAAG----1GENIChomozygous62162926
1143703268143703269GC22GENIChomozygous60878313
1143703436143703437TTA3GENIChomozygous61765911
1143703487143703488TC24GENIChomozygous60878316
1143703610143703611AG35GENICheterozygous60878317
1143703893143703897TTTA----15GENICheterozygous60878318
1143704813143704814TC52GENICheterozygous60878323
1143704869143704870GC31GENICheterozygous60878325
1143704888143704889AACT17GENICheterozygous60878326
1143704903143704904AACTT16GENICheterozygous60878327
1143705110143705111T-43GENICheterozygous60878329
1143705194143705195A-45GENICheterozygous60878331
1143705411143705414GCT---39GENICheterozygous61675302
1143708625143708626GA12GENIChomozygous61903038
1143708890143708891TC10GENICpossibly homozygous60878338
1143708905143708906TG9GENIChomozygous60878339
1143708926143708927AC16GENIChomozygous60878340
1143711403143711404CT19GENICpossibly homozygous61903039