chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 43250877 43250878 C CT 7 GENIC possibly homozygous 52371934 10 43250880 43250881 T - 7 GENIC heterozygous 52722379 10 43250977 43250981 CTTA ---- 17 GENIC homozygous 52147500 10 43252340 43252341 T C 13 GENIC homozygous 52147502 10 43253171 43253177 TTTTTT ------ 6 GENIC heterozygous 52371936 10 43253172 43253177 TTTTT ----- 6 GENIC heterozygous 52371938 10 43251051 43251054 TTC --- 16 GENIC homozygous 52190870 10 43252139 43252140 A AAGG 13 GENIC homozygous 52190872 10 43252262 43252263 T C 16 GENIC homozygous 52190874 10 43251054 43251055 G A 16 GENIC homozygous 52317294 10 43252690 43252691 C - 31 GENIC homozygous 51435069