chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101300117413001175GA19GENIChomozygous52029367
101300118313001184TTAC17GENIChomozygous51620362
101300124813001249GGCACACACACA6GENIChomozygous52356152
101300165413001678TTCTTTCTTTCTTTCTTTCTTTCT------------------------17GENIChomozygous52356154
101300370513003706GGAC17GENIChomozygous52029369
101300380413003805GGA8GENICheterozygous51620367
101300416313004164CT26GENIChomozygous52029371
101300429613004297TTCTCTCACACACACACA7GENICpossibly homozygous52356158
101300472713004728CT15GENIChomozygous51620370
101300546013005461TC11GENIChomozygous51620371
101300652613006527GGACCGACCA1GENIChomozygous52356160