chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1129282365129282367TG--14GENICheterozygous705633289
1129284219129284220TTC15GENIChomozygous705633292
1129288649129288650T-14GENICheterozygous705633293
1129294447129294448C-11GENICpossibly homozygous705633295
1129309633129309634AG6GENIChomozygous561879332
1129309634129309635CA6GENIChomozygous561879333
1129309641129309642AG9GENIChomozygous561879334
1129309648129309649A-12GENIChomozygous705633296
1129312135129312136A-8GENICheterozygous705633298
1129316827129316828A-15GENIChomozygous705633299
1129320755129320756CCAACACCT31GENIChomozygous705633301
1129320962129320963AAC39GENIChomozygous705633302
1129320981129320982AAC41GENIChomozygous705633303
1129320997129320998AAC44GENIChomozygous705633304
1129321017129321018TTC34GENIChomozygous705633305
1129321052129321053CT31GENIChomozygous561879335
1129321053129321054TC30GENIChomozygous561879336
1129325823129325824A-26GENICheterozygous705633306
1129328301129328302C-13GENIChomozygous705633307
1129328767129328768A-5GENICheterozygous705633309
1129330644129330645TTA2GENICheterozygous705633310
1129330654129330655GA7GENIChomozygous561879337
1129334737129334738CCT30GENIChomozygous705633311
1129337018129337019GGTTA17GENIChomozygous705633312
1129350885129350886G-8GENIChomozygous705633313
1129350909129350910GT10GENIChomozygous559759771
1129366067129366068TTTCTCTCTCTCTCTC5GENIChomozygous705633314
1129374391129374394ATA---5GENICheterozygous705633315
1129374412129374413AAT9GENICheterozygous705633316
1129375240129375241CCA53GENICheterozygous705633317
1129375279129375280AAT49GENICheterozygous705633318
1129375465129375466TTTCATAAAAGAAACTTTACTGAACTCAAAGCACACACTGCACCTCAC41GENICheterozygous705633319
1129378086129378087TTA26GENIChomozygous705633320
1129378947129378949AC--4GENICheterozygous705633321
1129384679129384680GGGGTGTGTGTGT7GENICheterozygous705633324
1129384679129384680GGGGTGTGTGTGTGT7GENICpossibly homozygous705633325