chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 60619766 60619767 T G 21 GENIC homozygous 998874249 18 60619776 60619777 T C 18 GENIC homozygous 998874250 18 60619778 60619779 T C 17 GENIC homozygous 998874251 18 60619780 60619781 T C 17 GENIC homozygous 998874252 18 60619782 60619783 T C 17 GENIC homozygous 998874253 18 60620465 60620466 T C 24 GENIC homozygous 998874254 18 60621236 60621237 C T 11 GENIC homozygous 998874255 18 60621238 60621239 C T 11 GENIC homozygous 998874256 18 60621240 60621241 C T 11 GENIC homozygous 998874257 18 60621346 60621347 G A 20 GENIC homozygous 998874258 18 60624249 60624250 G A 37 GENIC homozygous 998874259 18 60624297 60624298 T A 39 GENIC homozygous 998874260 18 60624298 60624299 A T 39 GENIC homozygous 998874261 18 60625800 60625801 T C 9 GENIC homozygous 998874262 18 60626242 60626243 A T 18 GENIC homozygous 998874263 18 60626632 60626633 T C 25 GENIC homozygous 998874264 18 60626871 60626872 C T 20 GENIC homozygous 998874265 18 60627484 60627485 T C 25 GENIC homozygous 998874266 18 60628800 60628801 A G 40 GENIC homozygous 998874267 18 60631251 60631252 C T 26 GENIC homozygous 998874268 18 60631509 60631510 G A 27 GENIC homozygous 998874269