chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153774644153774645GT19GENIChomozygous112890371
4153776733153776734TC23GENIChomozygous112890372
4153777091153777092CT17GENIChomozygous112890373
4153777965153777966CT19GENICpossibly homozygous112890374
4153778240153778241GT17GENIChomozygous112890375
4153778328153778329AT18GENIChomozygous112890376
4153776947153776947ACAGTCTC28GENIChomozygous128093356
4153780804153780805TC23GENIChomozygous112890377
4153782328153782328GGAGAGGG4GENIChomozygous128093357
4153782340153782342TA4GENIChomozygous128093358
4153782347153782349GA4GENIChomozygous128093359
4153782359153782360TG5GENIChomozygous112890378
4153782360153782361TG5GENIChomozygous112890379
4153782375153782376C6GENIChomozygous128093360
4153782383153782383G6GENIChomozygous128093361
4153782388153782388G6GENIChomozygous128093362
4153782393153782394AG4GENIChomozygous122146751
4153782411153782412T5GENIChomozygous128093365
4153782392153782392G5GENIChomozygous128093363
4153782401153782402G5GENIChomozygous128093364
4153783531153783532TC10GENIChomozygous112890380
4153784338153784339TC20GENIChomozygous112890381
4153785894153785894TTT16GENIChomozygous128093366
4153786114153786114A15GENIChomozygous128093367
4153789676153789677GA17GENIChomozygous112890385
4153790568153790569CT21GENIChomozygous112890386
4153790870153790871GA26GENIChomozygous112890387
4153790952153790953AG27GENIChomozygous112890388
4153790976153790977AC30GENIChomozygous112890389