chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155525507455255075TA18GENIChomozygous48314014
155525551155255512TTA11GENIChomozygous48314015
155525865855258659CT20GENIChomozygous48827806
155525883155258832CA6GENIChomozygous48314018
155526025555260256GGGGAT8GENIChomozygous48827808
155526133255261333CG11GENIChomozygous48827810
155526136655261367TC7GENIChomozygous48314020
155526140855261412AAAA----7GENIChomozygous49054476
155526141155261412AACTGT7GENIChomozygous49054478
155526141455261415AT8GENIChomozygous48602483
155526143355261434TC8GENIChomozygous48314021
155526144855261449AT9GENIChomozygous48314022
155526152255261526CACG----5GENIChomozygous49437556
155526170555261706TTATGTC10GENIChomozygous48314024
155526170755261708TTGCTATGGAGGAACCTCA10GENIChomozygous48314026
155526273755262738CG18GENICpossibly homozygous48827812
155526355155263552C-12GENICheterozygous49329578
155526413455264135AG11GENIChomozygous48827814
155526416755264168GA17GENIChomozygous48827816
155526424355264244CT31GENIChomozygous48827818
155526442855264438TGTGTGTGTG----------5GENIChomozygous49255432
155526530455265305AG23GENIChomozygous48827820
155526745255267453TA27GENIChomozygous48314030
155526745355267454TA27GENIChomozygous49255433
155526811355268114AAGAATGAAAGCTGCAAAGACCAGGGGTTCAGGAAAGTATTCTCTGCCCGGGTGAAACTGGCTGGGAGTGGGAAGGAGAGGTAGGAAGGGATGTGGAGAGTCAGGT23GENIChomozygous49054480
155526816055268161CT20GENIChomozygous48827822
155526817655268177CG22GENIChomozygous48314033
155526817855268179C-21GENIChomozygous48314034
155527145355271454GA13GENIChomozygous48314036
155527174955271750CG41GENIChomozygous48314037
155527184455271845CCGTGCGTGCGTGCGT6GENICheterozygous49255434
155527398055273981GGCA10GENICheterozygous49220972
155527552555275526AG31GENIChomozygous48827824
155527626555276266TTTTCCTTCCTTCCTTCCTTCC14GENIChomozygous49255435
155527703855277050CTTCCTTCCTTC------------11GENIChomozygous49054490
155527737255277374AT--2GENIChomozygous49407244
155527737555277376A-2GENIChomozygous49407245