chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 142108366 142108367 A 27 GENIC homozygous 131025758 7 142108595 142108596 T C 22 GENIC homozygous 116097456 7 142111295 142111296 A G 18 GENIC homozygous 116097458 7 142113026 142113026 A 30 GENIC possibly homozygous 131025759 7 142114193 142114194 C T 19 GENIC homozygous 116097460 7 142116047 142116048 C T 16 GENIC homozygous 115941387 7 142116249 142116250 T C 16 GENIC homozygous 115941388 7 142116258 142116259 C T 17 GENIC homozygous 115941389 7 142116946 142116947 A G 21 GENIC homozygous 115941391 7 142116993 142116994 T G 23 GENIC homozygous 116097462 7 142117902 142117903 T C 15 GENIC homozygous 116097464 7 142117905 142117909 GTGT 15 GENIC homozygous 131025760 7 142117968 142117969 C T 15 GENIC homozygous 122877561 7 142117989 142117995 GTGCGC 15 GENIC homozygous 131025761 7 142118001 142118002 G A 15 GENIC homozygous 122877563 7 142118004 142118005 C T 15 GENIC homozygous 116097470 7 142118015 142118019 GTGC 17 GENIC homozygous 131025762 7 142118023 142118025 GC 17 GENIC homozygous 131025763 7 142118028 142118029 T C 18 GENIC homozygous 122877566 7 142119389 142119390 A G 18 GENIC homozygous 115941394 7 142119769 142119770 C G 26 GENIC homozygous 115941396