chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75846351458463516TC--17GENICpossibly homozygous53930141
75847450558474508CCC---16GENICheterozygous53930145
75847450758474508C-16GENICheterozygous53930147
75848871558488716A-12GENICheterozygous53930149
75850629558506296GC24GENIChomozygous54655950
75850632558506326GGT13GENIChomozygous54420611
75851524958515250AG54GENICheterozygous53930153
75851727958517280AC15GENICheterozygous53930157
75852866358528664CT56GENIChomozygous53930161
75852923058529231TA37GENIChomozygous53930164
75853393058533931TA32GENICheterozygous54196064
75853388058533881CT37GENICheterozygous54196063
75854390358543904GC14GENIChomozygous53930168
75854402658544028AC--10GENICheterozygous54196068
75854405758544058C-4GENIChomozygous53930170
75854513158545132GGT19GENIChomozygous53930172
75855640358556404AAG1GENIChomozygous53930173
75856242558562426TTAC40GENIChomozygous53930175
75857059458570595AAT47GENIChomozygous53930179
75857093358570934G-37GENIChomozygous53930181
75858849258588493T-31GENIChomozygous53930185
75858853858588539TTA33GENIChomozygous53930187
75858873958588740G-18GENIChomozygous53930189
75858888458588885AATG8GENICpossibly homozygous53930190
75858940958589410GC5GENIChomozygous54196069
75859556358595564CA6GENICheterozygous53930194