chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228661582228661583GA1GENIChomozygous61604018
1228661637228661638TC2GENIChomozygous61107344
1228661888228661889GC21GENIChomozygous61107345
1228662170228662171GA29GENIChomozygous61107346
1228662747228662757GTGTGTGTGT----------16GENIChomozygous61604019
1228665193228665194TC18GENIChomozygous61107350
1228666073228666074GA18GENIChomozygous61604020
1228666556228666557CT14GENIChomozygous61604021
1228666717228666718GT18GENIChomozygous61604022
1228667082228667083CA23GENIChomozygous61604023
1228667493228667494CT25GENIChomozygous61604024
1228669606228669607GA26GENIChomozygous61107352
1228669631228669632TC19GENIChomozygous61107353
1228670146228670147AG17GENIChomozygous61107354
1228671386228671387GA13GENIChomozygous61107355
1228672371228672372CA8GENIChomozygous61604025
1228673205228673206A-14GENIChomozygous61604026
1228673616228673617CT27GENIChomozygous61107357
1228675201228675202TC28GENIChomozygous61107358
1228675312228675313CT30GENIChomozygous61107359
1228676534228676535GT17GENICpossibly homozygous61107362
1228676585228676586CCT7GENICheterozygous61107363
1228676585228676586CCTT7GENICheterozygous61107364
1228676609228676610GA7GENIChomozygous61604027
1228678104228678105AG20GENIChomozygous61107366
1228678931228678932AG26GENIChomozygous61107368
1228679272228679273TG20GENIChomozygous61604028