chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1203542986203542987CT22GENIChomozygous135791214
1203543104203543105TC21GENIChomozygous135791215
1203543873203543874CT16GENIChomozygous135791216
1203543984203543985G19GENIChomozygous402979263
1203543984203543985GT19GENICheterozygous402979264
1203543987203543988GT19GENIChomozygous135791217
1203544797203544798CT17GENIChomozygous135791218
1203545998203545999AG19GENIChomozygous135791219
1203546046203546046A20GENIChomozygous135455535
1203546110203546111AG23GENIChomozygous135791220
1203546280203546281AG22GENIChomozygous135791221
1203547890203547891AG28GENIChomozygous135791222
1203549001203549002CT20GENIChomozygous135791223
1203550599203550600GA28GENIChomozygous135791224
1203552161203552162AG24GENIChomozygous135791225
1203553268203553269GA16GENIChomozygous135791226
1203553289203553290GC14GENIChomozygous135791227
1203554128203554129TC24GENIChomozygous135791228
1203555588203555589GA20GENIChomozygous135791229
1203555649203555650GC14GENIChomozygous135791230
1203558973203558974CT10GENIChomozygous135791231
1203559263203559264TG16GENICheterozygous153906426
1203559263203559264T16GENIChomozygous402979265
1203559546203559547GA11GENIChomozygous135791232
1203559631203559632GA24GENIChomozygous135791233
1203560594203560597CCC1GENIChomozygous135455536
1203560608203560620CCCTCCTCCTCT1GENIChomozygous135455537
1203560675203560676CT7GENIChomozygous404127586
1203560675203560676C7GENICheterozygous404127587
1203560679203560680TC7GENIChomozygous135791234
1203560705203560706CT9GENIChomozygous403919619
1203560705203560706C9GENICheterozygous403919620
1203560715203560716CT10GENIChomozygous403919625
1203560715203560716C10GENICheterozygous403919626
1203560727203560728CT10GENIChomozygous403919629
1203560727203560728C10GENICheterozygous403919630
1203561064203561068ATCC10GENIChomozygous135455538
1203561211203561212TC20GENIChomozygous135791235