chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159717304397173044T-4GENICheterozygous722437382
159721500097215001T-20GENIChomozygous722437383
159722540297225403C-6GENIChomozygous722437384
159722541197225412T-5GENIChomozygous722437385
159722577197225772A-15GENIChomozygous722437386
159728209097282091CCAA2GENICheterozygous722437388
159729052997290530TA2GENIChomozygous588518158
159729053497290535GGA1GENIChomozygous722437389
159729053797290538TTA1GENIChomozygous722437390
159729054297290543AAG2GENIChomozygous722437391
159729271997292720G-6GENIChomozygous722437392
159729477697294777AAT7GENICpossibly homozygous722437393
159730880997308810A-8GENIChomozygous722437394
159730889297308893C-2GENIChomozygous722437397
159736199597361996TTC9GENICpossibly homozygous722437398
159736221297362213TTC5GENIChomozygous722437399
159736375297363753GA5GENICheterozygous588518159
159736404297364043GT6GENIChomozygous588435100