chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9113111606113111607A-22GENICheterozygous52116819
9113112586113112587AAC17GENICheterozygous52116837
9113112821113112822CT12GENIChomozygous52116841
9113113548113113549C-18GENIChomozygous52116843
9113115134113115135TTAA4GENICheterozygous52116845
9113115134113115135TTA4GENICheterozygous52116847
9113117280113117281GGGCGGCA11GENIChomozygous52116849
9113117387113117388CT21GENIChomozygous52116853
9113119143113119151ACAAACAA--------11GENIChomozygous52116855
9113120206113120207AG21GENIChomozygous52116857
9113120351113120352GA22GENIChomozygous52116859
9113120453113120465ACACACACACAC------------15GENICpossibly homozygous52919394
9113112168113112187CAAGGTGGTCATCTCTGAC-------------------33GENICheterozygous52919391
9113118553113118554CCTGTGTGTGTGTGTGTGTGTGTG5GENIChomozygous52919392
9113120451113120465ACACACACACACAC--------------15GENICheterozygous52919393
9113120842113120843TTA20GENIChomozygous52116863
9113123018113123019GA20GENIChomozygous52116865
9113123058113123059GA23GENIChomozygous52116867
9113123498113123499TTC6GENIChomozygous52116869
9113123562113123563CT16GENIChomozygous52116871
9113124037113124038CT18GENIChomozygous52116873
9113124674113124675TTA27GENIChomozygous52116875
9113125041113125042TC12GENIChomozygous52116877
9113125087113125088A-12GENIChomozygous52116879
9113125644113125645CA20GENIChomozygous52116881
9113126569113126570CT20GENIChomozygous52116883
9113126603113126604TC11GENIChomozygous52116885
9113127148113127163TGCTTTTCTTCTTTG---------------25GENICheterozygous53180068
9113127466113127467AAC19GENIChomozygous52116887
9113128500113128501GA28GENIChomozygous52116889
9113128982113128986TGTG----4GENIChomozygous52919395
9113129056113129057TC13GENIChomozygous52116893
9113129229113129230A-11GENICheterozygous52116895
9113129635113129636CT16GENIChomozygous52116897
9113129705113129706AAAAAAAAG8GENIChomozygous52868888
9113130049113130054GGTTC-----13GENICheterozygous52919397