chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2160180726160180729TTT---7GENICheterozygous60755830
2160180727160180729TT--7GENICheterozygous60503966
2160180921160180922GC9GENIChomozygous59188535
2160180923160180924GC9GENIChomozygous59188536
2160181752160181753GC18GENIChomozygous59188541
2160182115160182116GGA20GENICpossibly homozygous59188542
2160182271160182272TC21GENIChomozygous59188543
2160185128160185131CCC---14GENIChomozygous59188544
2160185663160185664AAT22GENIChomozygous59188545
2160186323160186324TTC24GENIChomozygous59188546
2160189793160189796ATG---26GENICheterozygous60453875
2160192308160192309AAT19GENIChomozygous59188549
2160192557160192558TC19GENIChomozygous59188550
2160192915160192916CG21GENIChomozygous59188551
2160193038160193039CT29GENIChomozygous59188552
2160193334160193335GT11GENIChomozygous59188553
2160193422160193423TTC2GENICheterozygous59188554
2160193668160193669CT15GENIChomozygous59188556
2160194006160194007TC21GENIChomozygous59188557
2160194365160194366GT23GENIChomozygous59188558
2160194808160194809GA26GENIChomozygous59188559
2160195443160195444A-27GENIChomozygous59188560
2160195485160195486CT30GENIChomozygous59188561
2160196006160196007AC28GENIChomozygous59188562
2160197090160197091GA12GENIChomozygous59188563
2160197909160197910GA29GENIChomozygous59188566
2160197997160197998GGA26GENICpossibly homozygous59188568
2160197998160197999GA29GENIChomozygous59188569
2160198687160198688G-23GENIChomozygous59188570
2160199257160199258AT15GENIChomozygous59188571
2160199258160199259CT14GENIChomozygous59188572
2160199909160199910CCCACACACACACA5GENIChomozygous60892627
2160200211160200212TC23GENIChomozygous59188574
2160201456160201460GTGT----3GENICheterozygous59188575
2160201458160201460GT--3GENICheterozygous59188576
2160202490160202491TC18GENIChomozygous59188577