chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122370146123701462G-27GENICheterozygous50129526
122370155923701561CG--22GENICheterozygous50597815
122370156023701561GGCA20GENICheterozygous50129530
122370157423701590ACTCACACACACACAA----------------29GENICheterozygous50597817
122370172123701733CACACACATACA------------55GENICheterozygous50538348
122370175423701755GGA54GENIChomozygous50129534
122370194823701949AAC12GENICheterozygous50129540
122370209923702100TG14GENIChomozygous50129542
122370236223702363T-16GENICheterozygous50129564
122370248923702490GC5GENIChomozygous50129572
122370272223702723AG13GENICheterozygous50129574
122370273323702734TTA15GENICheterozygous50129576
122370280323702804T-24GENICheterozygous50291388
122370297823702979AT6GENIChomozygous50129592
122370299823702999GGACTAGACTGGCCTT4GENIChomozygous50129594
122370310423703105AT29GENIChomozygous50129600
122370313523703136CT30GENICheterozygous50129602
122370320823703213TTTTG-----31GENICheterozygous50129610
122370321223703213GGT31GENICheterozygous50129612
122370352523703526TTC32GENIChomozygous50129648
122370391723703918GGT20GENICheterozygous50597819
122370453423704538CTGG----16GENICheterozygous50129688
122370462523704626A-17GENICheterozygous50129694
122370465823704660AC--12GENICheterozygous50129699
122370527823705279CCCTCCTCA1GENIChomozygous50129741
122370563923705640GGAC6GENIChomozygous50129772
122370772023707722AA--1GENIChomozygous50538350
122370967223709673T-4GENIChomozygous50538351
122370970723709712ACACT-----7GENIChomozygous50538352
122370974923709752TCT---11GENIChomozygous50538353
122371011523710116TA5GENIChomozygous50129856
122371039023710391C-14GENICheterozygous50597822