chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 91588590 91588591 G A 21 GENIC homozygous 54021304 7 91588733 91588734 T TAC 10 GENIC heterozygous 54021305 7 91588733 91588734 T TACACACACACAC 10 GENIC heterozygous 54021306 7 91588790 91588791 C T 25 GENIC homozygous 54021307 7 91588857 91588858 T - 26 GENIC homozygous 54021308 7 91588968 91588972 AAAG ---- 10 GENIC possibly homozygous 54021309 7 91588971 91588972 G - 13 GENIC homozygous 54021310 7 91589459 91589460 G A 32 GENIC homozygous 54021311 7 91590865 91590866 C A 21 GENIC homozygous 54021312 7 91591105 91591106 A G 25 GENIC homozygous 54021313 7 91592202 91592203 T C 39 GENIC homozygous 54208189 7 91591787 91591788 C T 26 GENIC homozygous 54208187 7 91591925 91591926 C - 27 GENIC homozygous 54208188 7 91591607 91591608 T C 30 GENIC homozygous 54021314 7 91591901 91591902 T C 24 GENIC homozygous 54021315 7 91591928 91591929 T - 27 GENIC homozygous 54021316 7 91592034 91592035 T C 20 GENIC homozygous 54021317 7 91592239 91592240 A C 40 GENIC homozygous 54208190 7 91592289 91592290 A G 33 GENIC homozygous 54208191 7 91592768 91592769 T A 21 GENIC possibly homozygous 54021319