chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10107364481107364482TC11GENIChomozygous116714321
10107365636107365637GA10GENIChomozygous117033988
10107365715107365716TC12GENIChomozygous116842231
10107366037107366038AT16GENIChomozygous116842233
10107366459107366460TC11GENIChomozygous116714331
10107366661107366662GA13GENIChomozygous116842235
10107368582107368583CT9GENIChomozygous116842239
10107368882107368883TG14GENIChomozygous116714341
10107370371107370372CT7GENIChomozygous116842241
10107370789107370790CT17GENIChomozygous116842243
10107371039107371040TC11GENIChomozygous116714359
10107372490107372491GA19GENIChomozygous116842245
10107373308107373309AG4GENIChomozygous116714361
10107373835107373836TC6GENIChomozygous116842247
10107374179107374180GT21GENIChomozygous116714365
10107374458107374459CT12GENIChomozygous116714367
10107374521107374522TA16GENIChomozygous116714369
10107375153107375154TC5GENIChomozygous118012695
10107375362107375363TC23GENIChomozygous116714371
10107375604107375605CG10GENICheterozygous116714373
10107375685107375686CT9GENIChomozygous116842249
10107375868107375869CT13GENIChomozygous116714375
10107375962107375963TC24GENIChomozygous116714377
10107376251107376252TC8GENIChomozygous116714379
10107376276107376277CA7GENIChomozygous116714381
10107376349107376350TG8GENIChomozygous116714383
10107376384107376385AG6GENIChomozygous116714385
10107376643107376644TC15GENIChomozygous116714387
10107377637107377638GA19GENIChomozygous116842251
10107377826107377827GA8GENIChomozygous116714391
10107377828107377829CG9GENIChomozygous116842253
10107377965107377966GA11GENIChomozygous116714393
10107378214107378215TA13GENIChomozygous116714395
10107378316107378317CT9GENIChomozygous116714397
10107378721107378722GA12GENIChomozygous116842255
10107378791107378792AG13GENIChomozygous116842257
10107379214107379215GA14GENIChomozygous116842259