chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141007701141007702TC10GENIChomozygous114031319
5141008255141008256TC8GENIChomozygous114031320
5141008529141008530TC13GENIChomozygous114031321
5141009739141009740TC7GENIChomozygous114031324
5141009874141009875GT16GENIChomozygous114031325
5141010013141010014CT20GENIChomozygous114031326
5141010775141010776AG16GENICheterozygous114031327
5141010900141010901AG10GENIChomozygous114031328
5141011168141011169AG8GENIChomozygous114031329
5141012136141012137AG6GENICheterozygous126205268
5141012461141012462TC7GENIChomozygous114031331
5141012981141012982GA15GENIChomozygous114031332
5141013782141013783CA18GENIChomozygous114031334
5141015950141015951GC6GENIChomozygous114031350
5141019372141019373GA4GENIChomozygous114031357
5141020090141020091AG21GENIChomozygous114031363
5141020730141020731CT9GENIChomozygous114031364
5141021100141021101CG13GENIChomozygous114031366
5141021976141021977GA8GENIChomozygous114031367
5141022148141022149TG8GENIChomozygous114031369
5141022623141022624TC15GENIChomozygous114031370
5141023119141023120TA8GENIChomozygous114031371
5141023503141023504AG6GENIChomozygous114031372
5141024940141024941AG15GENICheterozygous114031374
5141024947141024948AC12GENICheterozygous114031375
5141026064141026065GC16GENIChomozygous114031376
5141030061141030062GA6GENICheterozygous126240609
5141030464141030465TG9GENIChomozygous114031378
5141030561141030562TA19GENIChomozygous114031379
5141030627141030628GT10GENIChomozygous114031380
5141030711141030712TC11GENIChomozygous114031381
5141031083141031084TC12GENIChomozygous114031382
5141031657141031658AG19GENIChomozygous114031384