chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2160180727160180729TT--3GENICheterozygous60503966
2160180921160180922GC11GENIChomozygous59188535
2160180923160180924GC10GENIChomozygous59188536
2160181650160181651TA27GENIChomozygous60678805
2160182271160182272TC38GENIChomozygous59188543
2160183260160183261TG32GENIChomozygous60678807
2160183632160183633GA37GENIChomozygous60678809
2160183762160183766AAAC----21GENIChomozygous60678811
2160184539160184540GC40GENIChomozygous60678813
2160184752160184753CT22GENIChomozygous60678815
2160185196160185197TC31GENIChomozygous60678817
2160186201160186202AG24GENIChomozygous60678819
2160186732160186733CT28GENIChomozygous60678821
2160187316160187317AG37GENIChomozygous60678823
2160187944160187949TCCCC-----14GENIChomozygous60678825
2160187951160187952CA15GENIChomozygous60678827
2160188405160188406TC25GENIChomozygous60678829
2160188828160188829AC19GENIChomozygous60678831
2160189218160189219GA15GENIChomozygous60678833
2160190946160190947GGA16GENICpossibly homozygous60678835
2160191138160191139TTC30GENIChomozygous60678837
2160191394160191395TC19GENIChomozygous60678839
2160191536160191537GA24GENIChomozygous60678842
2160192046160192047TC31GENIChomozygous60678844
2160192257160192258CT31GENIChomozygous60678846
2160192309160192310TTC12GENIChomozygous60678848
2160192557160192558TC29GENIChomozygous59188550
2160193855160193862CACGGGT-------11GENIChomozygous60678850
2160196659160196660TA23GENICpossibly homozygous60148003
2160197090160197091GA26GENIChomozygous59188563
2160197757160197758AATAGG27GENIChomozygous60678852
2160198687160198688G-19GENIChomozygous59188570
2160200211160200212TC32GENIChomozygous59188574
2160201456160201460GTGT----17GENICheterozygous59188575
2160201458160201460GT--17GENICheterozygous59188576
2160202490160202491TC31GENIChomozygous59188577