chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41541584615415847AAT2GENICheterozygous57428544
41542433215424333C-1GENIChomozygous56763862
41545185615451857CCA13GENIChomozygous56763915
41547210515472106G-9GENIChomozygous57428558
41547245415472455TTAA3GENIChomozygous57428560
41547263015472631AG23GENICpossibly homozygous57428562
41547350215473503GA5GENIChomozygous56763949
41547404915474050CT1GENIChomozygous57428564
41547411315474114TC4GENIChomozygous57428566
41547526115475262C-6GENIChomozygous57428568
41547579615475797AG33GENICpossibly homozygous57428570
41547601815476019C-6GENIChomozygous57428572
41547644315476444AG4GENICheterozygous57428576
41547676715476768CCA8GENIChomozygous57428578
41547711215477113TC29GENICpossibly homozygous57428580