chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32034669520346696AG34GENIChomozygous141494203
32034705920347060TC40GENIChomozygous141494204
32034722820347229CA43GENIChomozygous141494205
32034736320347364CA36GENIChomozygous141494206
32034761920347620TC36GENIChomozygous141494207
32034771220347713CA51GENIChomozygous141494208
32034781620347817TC54GENIChomozygous141494209
32034792620347927TC44GENIChomozygous141494210
32034837120348372TC38GENIChomozygous141494211
32034841820348419CA38GENIChomozygous141494212
32034868620348687AC43GENICpossibly homozygous141494213
32034891120348912CT32GENIChomozygous141494214
32034893520348936CG37GENIChomozygous141494215
32035032920350330CA34GENIChomozygous141494216
32035057520350576GC31GENICpossibly homozygous141494217
32035058320350584GT30GENICheterozygous141494218
32035085820350859TG39GENICpossibly homozygous141494219
32035100420351005CG39GENIChomozygous136651008
32035140220351403GC34GENIChomozygous141494220
32035141720351418AC36GENIChomozygous141494221
32035149120351492CT30GENIChomozygous141494222
32035153920351540TC32GENIChomozygous141494223
32035181720351818AG31GENIChomozygous141494224
32035185720351858AC35GENIChomozygous136651009
32035189620351897GA36GENIChomozygous141494225
32035220020352201TG35GENIChomozygous141494226
32035223120352232CA34GENIChomozygous136651010
32035225720352258CT35GENIChomozygous141494227
32035236220352363CT44GENIChomozygous141494228
32035270420352705GA51GENIChomozygous136651011
32035270520352706CA51GENIChomozygous141494229
32034941520349416A35GENIChomozygous141471970
32035172020351720A37GENIChomozygous141471971
32035173220351733A35GENIChomozygous141471972
32035062120350622GC15GENICheterozygous145134231
32035062120350622G15GENICheterozygous403954658
32035057520350576G31GENICheterozygous403058830
32035058320350584G30GENICheterozygous403058831