chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2135432474135432475CT33GENIChomozygous136294293
2135432813135432814AT44GENIChomozygous136294294
2135433122135433123GA51GENIChomozygous136294295
2135433626135433626TG32GENIChomozygous135944251
2135433933135433934TC32GENICpossibly homozygous136294296
2135435591135435592A31GENIChomozygous135944252
2135435616135435617AG32GENIChomozygous136294297
2135435648135435649GA35GENIChomozygous136294298
2135436047135436048AT47GENIChomozygous136294299
2135436182135436183GA30GENIChomozygous136294300
2135436536135436537CA37GENIChomozygous136294301
2135436726135436726A41GENIChomozygous135944253
2135436821135436822CT48GENIChomozygous136294302
2135437193135437194AG44GENIChomozygous136294303
2135438031135438031AGAGG13GENICheterozygous135944255
2135438033135438033AGAGG14GENICheterozygous145130032
2135438949135439062AAAAAAATGAAGGAACGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAACCCAAAAAAAAA23GENIChomozygous135944257
2135439131135439132AG32GENIChomozygous136294304
2135439231135439232TC42GENIChomozygous136294305
2135433830135433834AAGA12GENICheterozygous144580306