chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3100354083100354085AC--4GENICheterozygous58807792
3100356792100356793TTAA15GENICpossibly homozygous57578351
3100356792100356793TTA15GENICheterozygous57930573
3100371654100371655CCA4GENICheterozygous58617226
3100374377100374378CCAGCG2GENIChomozygous58617227
3100374385100374386T-3GENIChomozygous57578375
3100374400100374401CCG2GENIChomozygous57578377
3100374425100374426GGC1GENIChomozygous57578379
3100374427100374428GGC1GENIChomozygous57578381
3100397448100397449T-20GENIChomozygous57578389
3100400729100400731TT--21GENIChomozygous58555486
3100400733100400734TA24GENIChomozygous58555487
3100400734100400735TA24GENIChomozygous58555488
3100400736100400737TTAGAG24GENIChomozygous58617228
3100400737100400738TG24GENIChomozygous58617229
3100400744100400745AT25GENIChomozygous57578393
3100400749100400750AT24GENIChomozygous57578395
3100400768100400769TG21GENIChomozygous57578397
3100400771100400772TG23GENIChomozygous57578399
3100400773100400774TA25GENIChomozygous57578401
3100400777100400778TG26GENIChomozygous57578403
3100400784100400785TG26GENIChomozygous57578405
3100400790100400791AT27GENIChomozygous57578407
3100406116100406117GGA16GENICheterozygous58670579
3100406117100406118A-16GENICheterozygous58670581
3100406538100406539CCAGTGGTAGAGTGCT16GENIChomozygous58617231
3100406685100406686AAG3GENIChomozygous57578413
3100406720100406721TTCATGTGGGTGCTGGGATTTGAACTCAGAACCTCTGGAAGAGCTGTCAGTGCTCTTAACACTGAGCCATC2GENIChomozygous58670583
3100408655100408656A-13GENICheterozygous57578415
3100412039100412043GTGT----6GENICheterozygous58856009
3100417310100417319CTGTCAGGT---------23GENIChomozygous57578421
3100417327100417328CCA20GENIChomozygous57578423
3100418781100418782TTAAAAGAGCA27GENIChomozygous57578425
3100421607100421608CT16GENIChomozygous57578427
3100424567100424568A-5GENIChomozygous58670585
3100425546100425548AC--9GENICheterozygous58670587