chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109216387109216389GT--21GENIChomozygous737519015
6109216449109216450AC33GENIChomozygous616052090
6109216711109216712CG27GENIChomozygous616052091
6109217708109217709GA35GENIChomozygous616052092
6109217869109217870CCT13GENICheterozygous737519016
6109217869109217870CCTT13GENICheterozygous737519017
6109218078109218079TG17GENIChomozygous616052093
6109218132109218133GA29GENIChomozygous616052094
6109218533109218534TC37GENIChomozygous613922342
6109218971109218972CG29GENIChomozygous616052095
6109219610109219614TTTT----15GENICheterozygous737519018
6109219611109219614TTT---15GENICpossibly homozygous737519019
6109219618109219619TTAAA15GENICheterozygous737519021
6109219618109219619TTAA15GENICpossibly homozygous737519022
6109219644109219645CG12GENIChomozygous616052096
6109219668109219669TC6GENIChomozygous616052097
6109219684109219685GGTCGTTTGGTCAGTTTC4GENIChomozygous737519023
6109219686109219687CCCGA1GENIChomozygous737519024
6109219945109219946GA29GENIChomozygous616052098
6109220171109220172AG24GENIChomozygous613922343
6109221203109221204T-12GENICpossibly homozygous737519025
6109221479109221480AG41GENIChomozygous613922344
6109222374109222375TTTCCAGCCC21GENIChomozygous737519027
6109222377109222378TTTGTTTTATTTAATAACCCA2GENIChomozygous737519028
6109224251109224252CT41GENIChomozygous616052099
6109224345109224346CCTT5GENICheterozygous737519029
6109224345109224346CCTTT5GENICheterozygous737519030
6109224503109224504CT13GENICpossibly homozygous613922345
6109225632109225633TC36GENIChomozygous613922346
6109225969109225970GC11GENIChomozygous613922347
6109226303109226304G-31GENIChomozygous737519031
6109227067109227069GA--3GENICheterozygous737519033
6109227068109227069AT3GENICheterozygous616052100
6109227301109227302CCTGTT12GENIChomozygous737519038
6109227384109227385TC30GENIChomozygous613922348
6109227512109227513TA29GENIChomozygous616052101
6109228010109228011GA33GENIChomozygous616052102