chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47065588770655888AT17GENIChomozygous113032533
47065601270656013TC19GENIChomozygous113032534
47065607970656080CT11GENIChomozygous113032535
47065610070656101GT24GENIChomozygous113032536
47065612470656125CG17GENIChomozygous113032537
47065631370656314AG6GENICheterozygous126049780
47065642570656426AG11GENIChomozygous113032542
47065642970656430TA10GENIChomozygous113032543
47065651570656516CT10GENIChomozygous113032544
47065651870656519AC8GENIChomozygous113032545
47065655270656553TG10GENIChomozygous113032546
47065655670656557AT7GENIChomozygous113032547
47065655770656558CG7GENIChomozygous113032548
47065662470656625GC22GENIChomozygous113032549
47065674270656743CG7GENIChomozygous113032550
47065708770657088TC15GENIChomozygous113032555
47065723970657240TC6GENIChomozygous112700921
47065726770657268AT5GENIChomozygous113349627
47065738870657389AG24GENIChomozygous113032556
47065751570657516GA16GENIChomozygous113032557
47065757570657576TG28GENIChomozygous113032558
47065764470657645AT15GENIChomozygous113032559
47065764570657646GC15GENIChomozygous113032560
47065767370657674AC12GENIChomozygous113032561
47065819770658198GA7GENIChomozygous113349629
47065885470658855GA24GENIChomozygous113032568
47065908870659089AG16GENIChomozygous113032570