chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242960170242960170C17GENIChomozygous141181050
1242960237242960238GA15GENIChomozygous141305308
1242960297242960297CACAATTTTACTTGTGAGCAGTGTCTTC15GENIChomozygous141181051
1242960641242960642GA15GENIChomozygous141305309
1242963395242963396AC23GENIChomozygous135851770
1242964999242965000GC16GENIChomozygous135851771
1242965635242965636GA21GENIChomozygous141305310
1242966962242966963GA19GENIChomozygous135851772
1242967738242967739GA16GENIChomozygous141305311
1242967830242967831CT19GENIChomozygous141305312
1242968706242968707CT18GENIChomozygous141305313
1242968720242968721TC18GENIChomozygous135851774
1242970733242970734CA13GENIChomozygous141305314
1242973774242973775TC27GENIChomozygous135851778
1242974134242974135GA29GENIChomozygous141305315
1242976241242976242AT15GENIChomozygous141305316
1242977621242977622CT20GENIChomozygous141305317
1242978739242978740AG9GENICpossibly homozygous135851780
1242978767242978768GA8GENIChomozygous135851781
1242971707242971708C26GENIChomozygous402983516
1242978767242978768G8GENICheterozygous402983517
1242971707242971708CT26GENICheterozygous153920250
1242964999242965000G16GENICheterozygous402983515
1242965012242965013CT17GENICheterozygous403549014
1242965012242965013C17GENIChomozygous403549015
1242978877242978878AC16GENIChomozygous135851782
1242978922242978923GC14GENIChomozygous135851783
1242979514242979515GT8GENIChomozygous135851784
1242979753242979754AC25GENIChomozygous141305318
1242980705242980706CT18GENIChomozygous135851786
1242980858242980859A10GENIChomozygous135469572
1242983774242983775TA23GENIChomozygous135851787
1242985071242985072TC24GENIChomozygous135851789
1242988085242988086GA23GENIChomozygous141305319
1242988349242988350TC23GENIChomozygous135851792
1242989549242989550AG21GENIChomozygous135851793
1242990302242990303GA22GENIChomozygous135851794
1242991967242991968AG31GENIChomozygous135851795
1242994014242994015TA20GENIChomozygous141305320
1242994902242994903GA17GENIChomozygous141305321