chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1105207223105207224GGACA1GENIChomozygous61491696
1105207501105207502AT26GENIChomozygous61491699
1105207708105207709GT10GENIChomozygous62148289
1105207710105207711GT11GENIChomozygous62148291
1105207712105207713GT11GENIChomozygous62148293
1105207713105207714GGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAT19GENIChomozygous62085483
1105207883105207884TC27GENIChomozygous61737353
1105212116105212117CT24GENIChomozygous61737355
1105212880105212884GATA----2GENIChomozygous62148297
1105212957105212958AG29GENIChomozygous61491720
1105213674105213675CT19GENIChomozygous61737357
1105213758105213759GA23GENIChomozygous61737359
1105213915105213916TG22GENIChomozygous61737361
1105214154105214155A-19GENIChomozygous61737363
1105214252105214253AG23GENIChomozygous61737365
1105214335105214336GA22GENIChomozygous61737367
1105214416105214417CT23GENIChomozygous61737369
1105214436105214437TG32GENIChomozygous61737371
1105215229105215230GA43GENIChomozygous61737373
1105219382105219383AG26GENIChomozygous61737375
1105219473105219474AAGTGTGT8GENICheterozygous61491734
1105219473105219474AAGTGT8GENICheterozygous61491735
1105221107105221108TTGACA27GENIChomozygous61491736
1105222120105222121CCCTG27GENIChomozygous62085484
1105222652105222653TC30GENIChomozygous61491739
1105222773105222774GC29GENIChomozygous61737377
1105224362105224363TC27GENIChomozygous61737379