chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46211411162114112AAT6GENICheterozygous56917971
46211412062114121TTC7GENIChomozygous57935257
46211429562114296CCT17GENICpossibly homozygous57935259
46211469362114694GT24GENIChomozygous56917972
46211519162115192GA19GENIChomozygous57935261
46211528262115283AG22GENIChomozygous56917975
46211532262115323TC23GENIChomozygous56917976
46211536462115365TC19GENIChomozygous57330549
46211539062115391AG16GENIChomozygous57330551
46211539562115400TTTTT-----11GENIChomozygous56917977
46211540162115402T-11GENIChomozygous56917978
46211551162115512TC32GENIChomozygous56917980
46211613562116139ACAG----19GENIChomozygous56917981
46211625062116251GA30GENIChomozygous57733221
46211712862117129GC32GENIChomozygous56917984
46211795762117958GA22GENIChomozygous57733223
46211835662118357GA24GENIChomozygous57733225
46211863662118637TG24GENIChomozygous56917987
46211886062118861CT10GENIChomozygous57733227
46211888862118889TC10GENIChomozygous56917988
46211889162118893AA--8GENIChomozygous57330561
46211990062119901CG28GENIChomozygous56917991
46212021962120220CG49GENIChomozygous56917992
46212035962120360CA31GENIChomozygous57733229
46212055362120554TTCCTGGCACATCC9GENIChomozygous56917993
46212055562120556T-16GENICheterozygous56917994
46212088362120884TC22GENIChomozygous56917995
46212096362120964GA30GENIChomozygous57733231
46212148862121489AATG15GENIChomozygous57733233
46212150762121511TTCT----11GENIChomozygous56917997
46212151562121516TC15GENICheterozygous56917998
46212154062121544TCTT----12GENICheterozygous56918000
46212154262121547TTTCT-----12GENIChomozygous56918001
46212232462122325TC36GENIChomozygous56918004
46212350362123506AAA---11GENIChomozygous57733235
46212375762123758GA20GENIChomozygous57733237
46212381762123818CA25GENIChomozygous57733239