chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 146773041 146773042 C T 21 GENIC homozygous 137226726 4 146773309 146773310 C T 14 GENIC homozygous 137226727 4 146773869 146773870 T A 21 GENIC homozygous 137226729 4 146773872 146773873 T C 20 GENIC homozygous 137226730 4 146774054 146774055 T 13 GENIC homozygous 136920019 4 146774060 146774061 A G 14 GENIC homozygous 137226731 4 146774414 146774415 T 23 GENIC homozygous 136920020 4 146774676 146774676 TGAGCCATCGTGTCTTTAG 25 GENIC homozygous 136920021 4 146774680 146774680 T 26 GENIC homozygous 136920022 4 146774682 146774682 CTGT 25 GENIC homozygous 136920023 4 146775050 146775051 T A 24 GENIC homozygous 137226734 4 146775095 146775096 T C 26 GENIC homozygous 137226735 4 146775119 146775119 A 28 GENIC homozygous 136920024 4 146775773 146775774 G A 26 GENIC homozygous 137226736 4 146775819 146775820 G A 26 GENIC homozygous 137226737 4 146776366 146776367 T C 24 GENIC homozygous 137226739 4 146776724 146776725 A G 16 GENIC homozygous 137226741 4 146776887 146776888 G A 27 GENIC homozygous 137226742 4 146776992 146776993 A G 31 GENIC homozygous 137226743 4 146777522 146777523 A G 16 GENIC homozygous 137226744 4 146777760 146777761 T C 24 GENIC homozygous 137226745 4 146778227 146778228 A G 16 GENIC homozygous 137226747 4 146779096 146779097 A G 29 GENIC homozygous 137226748 4 146776696 146776697 C T 21 GENIC homozygous 146424537 4 146777622 146777623 C A 17 GENIC homozygous 146424538