chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 14611163 14611164 T C 31 GENIC homozygous 109102903 20 14612584 14612585 A G 43 GENIC homozygous 109102905 20 14617121 14617122 A G 39 GENIC homozygous 109102922 20 14618066 14618067 T C 32 GENIC homozygous 109102926 20 14620660 14620661 C T 39 GENIC homozygous 109303570 20 14622004 14622005 C G 49 GENIC homozygous 109102936 20 14622424 14622425 G A 34 GENIC homozygous 109102940 20 14625835 14625836 G A 41 GENIC homozygous 109303574 20 14627421 14627422 G A 40 GENIC homozygous 109303576 20 14627542 14627543 C T 36 GENIC homozygous 109303578 20 14627774 14627775 G A 42 GENIC homozygous 109303580 20 14629271 14629272 C T 46 GENIC homozygous 109102967 20 14629537 14629538 A T 41 GENIC homozygous 109303582 20 14630469 14630470 G A 30 GENIC homozygous 109102973 20 14630604 14630605 C T 29 GENIC homozygous 109303584 20 14632420 14632421 T C 40 GENIC possibly homozygous 109303586 20 14634543 14634544 C G 53 GENIC homozygous 109303588 20 14635772 14635773 C T 39 GENIC possibly homozygous 109303590 20 14636602 14636603 A G 32 GENIC homozygous 109102993 20 14639215 14639216 T C 29 GENIC homozygous 109102997 20 14639494 14639495 C T 31 GENIC homozygous 109303592 20 14639929 14639930 T C 82 GENIC heterozygous 119871753 20 14639979 14639980 C G 65 GENIC heterozygous 119871754 20 14639982 14639983 C T 67 GENIC heterozygous 119871756 20 14640632 14640633 C T 39 GENIC homozygous 109303594 20 14640930 14640931 C T 30 GENIC homozygous 109103005 20 14643592 14643593 A G 28 GENIC homozygous 109303596