chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104793117347931174TA20GENICpossibly homozygous117178270
104793144447931445TG22GENIChomozygous116878977
104793253347932534GA16GENIChomozygous117178271
104793600047936001GT18GENIChomozygous116588121
104793738147937382TC38GENIChomozygous116588123
104793772747937728TC23GENIChomozygous116588125
104793772847937729AT22GENIChomozygous116588127
104793858047938581AG21GENIChomozygous116588129
104793935847939359GT20GENIChomozygous116588133
104794020647940207TC21GENIChomozygous116588135
104794205047942051GA11GENIChomozygous116588137
104794465347944654AC5GENICheterozygous116588141
104794465547944656AC5GENICheterozygous117178272
104794478547944786TG22GENIChomozygous116588143
104794566247945663CT21GENIChomozygous116588145
104794576947945770TC22GENIChomozygous116588147
104794673747946738AG17GENIChomozygous117178273
104794803947948040AC28GENIChomozygous116588153
104794804947948050TC28GENIChomozygous116588155
104794840547948406CT11GENIChomozygous116588157
104794880947948810CT20GENICpossibly homozygous117178274
104794924947949250AG23GENIChomozygous116588159
104794938347949384AG22GENIChomozygous117178275