chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 60619766 60619767 T G 21 GENIC homozygous 962598992 18 60619776 60619777 T C 15 GENIC homozygous 962598993 18 60619778 60619779 T C 14 GENIC homozygous 962598994 18 60619780 60619781 T C 15 GENIC homozygous 962598995 18 60619782 60619783 T C 18 GENIC homozygous 962598996 18 60620465 60620466 T C 26 GENIC homozygous 962598997 18 60620603 60620604 T C 22 GENIC homozygous 962598998 18 60621236 60621237 C T 19 GENIC heterozygous 962598999 18 60621238 60621239 C T 19 GENIC homozygous 962599000 18 60621240 60621241 C T 19 GENIC homozygous 962599001 18 60621346 60621347 G A 27 GENIC homozygous 962599002 18 60624249 60624250 G A 28 GENIC possibly homozygous 962599003 18 60624297 60624298 T A 29 GENIC homozygous 962599004 18 60624298 60624299 A T 29 GENIC homozygous 962599005 18 60625800 60625801 T C 17 GENIC homozygous 962599006 18 60626242 60626243 A T 26 GENIC homozygous 962599007 18 60626632 60626633 T C 15 GENIC homozygous 962599008 18 60626871 60626872 C T 20 GENIC homozygous 962599009 18 60627484 60627485 T C 19 GENIC homozygous 962599010 18 60628800 60628801 A G 18 GENIC homozygous 962599011 18 60631251 60631252 C T 35 GENIC homozygous 962599012 18 60631509 60631510 G A 34 GENIC homozygous 962599013