chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 12075589 12075590 G C 26 GENIC homozygous 53790178 7 12076297 12076298 T C 26 GENIC homozygous 53790179 7 12076880 12076881 G C 38 GENIC homozygous 53790180 7 12076895 12076896 G C 37 GENIC homozygous 53790181 7 12076900 12076901 T C 33 GENIC homozygous 53790182 7 12077379 12077380 C G 18 GENIC possibly homozygous 53790183 7 12077868 12077869 T C 26 GENIC homozygous 53790184 7 12078033 12078034 C T 13 GENIC homozygous 53790185 7 12078038 12078039 A ACC 6 GENIC homozygous 54629905 7 12078441 12078442 G A 11 GENIC homozygous 53790188 7 12078938 12078939 T C 30 GENIC homozygous 53790189 7 12081379 12081380 C T 30 GENIC homozygous 53790192 7 12081634 12081635 A G 26 GENIC homozygous 53790193 7 12081869 12081870 A G 27 GENIC homozygous 53790194 7 12082905 12082906 T G 27 GENIC homozygous 53790195 7 12078085 12078091 TTTTTT ------ 6 GENIC heterozygous 54954750 7 12078086 12078091 TTTTT ----- 6 GENIC heterozygous 54954752 7 12078294 12078295 T C 37 GENIC homozygous 54711066 7 12083965 12083966 A G 26 GENIC homozygous 54711068 7 12085797 12085800 TTT --- 16 GENIC heterozygous 55057491 7 12085798 12085800 TT -- 16 GENIC possibly homozygous 54954754