chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----8GENIChomozygous714038253
3154514276154514277TG13GENIChomozygous572697007
3154514414154514415AAGTCT16GENIChomozygous714038255
3154514475154514476TC12GENIChomozygous572697008
3154514477154514478TC12GENIChomozygous572697009
3154515475154515476GA12GENIChomozygous572697010
3154515681154515682TA38GENIChomozygous572697011
3154516008154516009GA32GENIChomozygous572697012
3154516009154516010AT32GENIChomozygous572697013
3154516260154516261TC26GENIChomozygous572697014
3154516884154516885AG37GENIChomozygous572697015
3154517077154517078TC26GENIChomozygous574698949
3154517156154517157AG18GENIChomozygous572697016
3154517593154517594TC28GENIChomozygous572697017
3154517632154517633G-23GENIChomozygous714038256
3154517898154517899TC24GENIChomozygous572697018
3154517982154517986GGCA----23GENIChomozygous714038257
3154518068154518069GA35GENIChomozygous572697019
3154518158154518159TTA46GENIChomozygous714038258
3154518562154518563CT39GENIChomozygous574698950
3154518737154518738AG19GENIChomozygous572697020
3154518931154518932GGT13GENICpossibly homozygous714038259
3154519100154519101CT16GENIChomozygous574698951
3154519184154519185CCA17GENICpossibly homozygous714038260
3154519315154519316CT25GENIChomozygous572697021
3154519896154519897CCTT29GENIChomozygous714038263
3154519985154519986AG21GENIChomozygous572697022
3154520058154520059TC23GENIChomozygous572697023
3154520781154520782TC31GENIChomozygous572697024
3154520987154520988CT26GENIChomozygous572697025
3154521914154521915TTAA1GENIChomozygous714038265
3154521930154521931AAC2GENICheterozygous714038266
3154522134154522135AG36GENIChomozygous572697026