chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 907487 907488 C CGTGT 9 GENIC homozygous 46041908 19 909386 909387 G GTT 7 GENIC homozygous 46041912 19 910162 910165 TTG --- 21 GENIC homozygous 46206885 19 910886 910887 C T 28 GENIC homozygous 46041918 19 911263 911264 T A 13 GENIC homozygous 46041920 19 911378 911379 G A 14 GENIC homozygous 46041922 19 911583 911584 G A 14 GENIC homozygous 46206886 19 911762 911763 T C 16 GENIC homozygous 46041926 19 911783 911786 TGT --- 12 GENIC homozygous 46206887 19 912112 912113 A G 20 GENIC homozygous 46041928 19 912144 912145 C T 11 GENIC homozygous 46041930 19 912147 912148 C T 12 GENIC homozygous 46041932 19 912399 912400 T TGAGA 19 GENIC homozygous 46041934 19 912431 912436 TTTGT ----- 11 GENIC homozygous 46041938 19 912619 912620 G T 16 GENIC homozygous 46041940 19 912678 912679 C T 10 GENIC homozygous 46041942 19 912757 912758 T C 17 GENIC homozygous 46041944 19 912875 912876 A AGGG 7 GENIC homozygous 46041946 19 913311 913312 G A 16 GENIC homozygous 46041952 19 913411 913412 T C 20 GENIC homozygous 46041954 19 913537 913538 T C 14 GENIC homozygous 46041956 19 913962 913963 A G 14 GENIC homozygous 46041960 19 914021 914022 G A 11 GENIC homozygous 46041962 19 914129 914130 T C 24 GENIC homozygous 46041964 19 914199 914200 T C 21 GENIC homozygous 46041966 19 914235 914236 T C 20 GENIC homozygous 46041968 19 914609 914610 G A 26 GENIC homozygous 46041970 19 915033 915034 C G 11 GENIC homozygous 46041974 19 915148 915149 T C 22 GENIC homozygous 46041976 19 915229 915230 A AAAAC 22 GENIC homozygous 46041978 19 915341 915342 C G 13 GENIC homozygous 46041980 19 915408 915409 C CT 9 GENIC homozygous 46041982 19 915500 915501 T C 45 GENIC homozygous 46206889