chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2256758339256758340CT17GENIChomozygous111042514
2256759600256759601CT15GENIChomozygous111042516
2256759766256759767GC4GENIChomozygous111042518
2256759778256759779TC7GENIChomozygous110863068
2256760616256760617AG21GENIChomozygous110863076
2256760637256760638GC23GENIChomozygous111042524
2256760737256760738GT16GENIChomozygous110863078
2256760742256760743GA14GENIChomozygous111042526
2256760998256760999AC13GENIChomozygous111042528
2256761023256761024AG12GENIChomozygous111042530
2256762420256762421GA16GENIChomozygous110863092
2256762460256762461GA15GENIChomozygous110863094
2256762524256762525AG11GENIChomozygous110863096
2256762738256762739TC9GENIChomozygous110863098
2256763012256763013GC16GENIChomozygous110863104
2256763027256763028AG16GENIChomozygous110863106
2256763362256763363TG19GENIChomozygous110863108
2256763595256763596TC20GENIChomozygous110863110
2256764117256764118AG6GENIChomozygous120163854
2256764203256764204CT11GENIChomozygous110863112
2256765554256765555TC17GENIChomozygous110863128
2256765910256765911GA14GENIChomozygous110863130
2256766039256766040GC11GENIChomozygous110863132
2256766433256766434CT12GENIChomozygous111042540
2256766451256766452TC15GENIChomozygous110863134
2256766564256766565TG19GENIChomozygous110863136
2256766579256766580TC20GENIChomozygous110863138
2256766769256766770CT11GENICheterozygous110863140
2256767808256767809TC17GENIChomozygous111042542
2256767993256767994GC7GENIChomozygous111042544
2256767995256767996GA5GENIChomozygous111042546
2256768508256768509TC20GENIChomozygous111042548
2256768574256768575AG20GENIChomozygous110863160
2256768650256768651GA7GENIChomozygous120177454
2256768652256768653TG6GENIChomozygous120177455
2256768674256768675GA8GENIChomozygous110863162
2256768804256768805GA24GENIChomozygous110863164
2256768969256768970TA23GENIChomozygous110863166
2256769146256769147AG28GENIChomozygous110409119