chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105864031858640320CC--7GENIChomozygous51661761
105864481658644817TA18GENIChomozygous52061722
105864563958645640CA15GENIChomozygous51464238
105864564258645643CT15GENIChomozygous51464239
105864565658645657TA15GENIChomozygous52061724
105864566158645662CT15GENIChomozygous52061726
105864579858645799CT9GENIChomozygous51661769
105864605858646059GGA8GENIChomozygous51661773
105864628758646288TC14GENIChomozygous51661775
105864699258646993TG12GENIChomozygous51661777
105864701558647016A-14GENIChomozygous51661779
105865081958650821GT--16GENIChomozygous51661781
105865424458654245TC18GENIChomozygous51464267
105865454958654550GA17GENICheterozygous51464276
105865456458654565TC11GENICheterozygous51464277
105865565558655656TC10GENIChomozygous51464297
105865566958655670CCTTGT12GENIChomozygous51464298
105865589958655900TC12GENIChomozygous51464299
105865607858656079GA11GENIChomozygous52061728
105865621358656214GA9GENIChomozygous51661813
105865750958657510CG15GENIChomozygous51661816
105865790758657908CA17GENIChomozygous51464303
105865858958658590TC7GENIChomozygous51464307
105865867358658674TTTC7GENIChomozygous51464308
105865972258659723T-7GENIChomozygous51661830
105865986458659865GA16GENIChomozygous52061730
105866028458660285CT12GENIChomozygous51464312
105866038858660389AAT8GENIChomozygous51661832
105866040358660404AATTTTAT11GENIChomozygous52460732
105866041158660412A-11GENIChomozygous52460733
105866119758661198AC12GENIChomozygous51661836
105866211458662115CT18GENIChomozygous51661838
105866288558662886CA18GENIChomozygous51661840
105866306958663070TG17GENIChomozygous51464318