chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139840228798402288TTACAC13GENICpossibly homozygous711106735
139840331998403323TTTT----12GENIChomozygous711106736
139840415398404154AG17GENIChomozygous571682164
139840632598406326TC15GENIChomozygous568765004
139840693198406932G-4GENIChomozygous711106738
139840693898406939C-4GENIChomozygous711106739
139840791798407918CT27GENIChomozygous568765005
139840800798408008G-20GENIChomozygous711106740
139840863698408637CT17GENIChomozygous571682165
139840907698409077GA26GENIChomozygous571682166
139840972298409723CT32GENIChomozygous568765006
139841027898410279AG27GENIChomozygous571682167
139841176898411769CT18GENIChomozygous571682168
139841227798412278T-13GENICpossibly homozygous711106741
139841329198413292AG20GENIChomozygous568765007
139841427898414279A-9GENIChomozygous711106744
139841472398414724AAT5GENICheterozygous711106746
139841472398414724AATTTTTT5GENICheterozygous711106747
139841700998417010CT8GENIChomozygous571682169
139841704298417043GA7GENIChomozygous571682170
139841771198417712GC19GENIChomozygous568765008
139841806298418063CT17GENIChomozygous568765009
139841810598418106AG24GENIChomozygous568765010
139841810998418110TC19GENIChomozygous568765011
139841844698418450GAAA----13GENIChomozygous711106748
139841855398418554T-14GENIChomozygous711106749
139841887098418871GA26GENIChomozygous568765012
139842193698421937GC21GENIChomozygous568765013
139842217398422174CT24GENIChomozygous571682171
139842250898422509CT17GENIChomozygous571682172
139842307498423075AC27GENIChomozygous568765014
139842378198423782GA17GENIChomozygous571682173
139842418098424181AG15GENIChomozygous571682174
139842576398425764TC25GENIChomozygous571682175
139842735298427353GT26GENIChomozygous568765015