chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 62122671 62122672 T TG 7 GENIC homozygous 724102796 8 62124790 62124791 T C 19 GENIC homozygous 590447158 8 62125167 62125168 G T 12 GENIC homozygous 590447159 8 62125174 62125175 G GA 11 GENIC homozygous 724102797 8 62125724 62125725 T G 9 GENIC possibly homozygous 590447160 8 62126765 62126766 T C 14 GENIC homozygous 590447161 8 62127609 62127610 G A 12 GENIC heterozygous 590447162 8 62127639 62127640 C T 8 GENIC homozygous 591782640 8 62132718 62132719 C G 9 GENIC possibly homozygous 591782641 8 62133017 62133018 C T 17 GENIC homozygous 591782642 8 62133600 62133601 T A 13 GENIC homozygous 591782643 8 62134345 62134346 C T 7 GENIC heterozygous 591782644 8 62134519 62134520 C A 4 GENIC homozygous 591782645 8 62136203 62136204 T C 7 GENIC homozygous 590447163 8 62137713 62137714 G A 8 GENIC homozygous 591782646 8 62138042 62138043 C T 17 GENIC possibly homozygous 591782647 8 62140309 62140310 G A 7 GENIC possibly homozygous 591782648 8 62140790 62140791 A G 11 GENIC heterozygous 590447164 8 62141096 62141097 C T 5 GENIC heterozygous 591782649 8 62142485 62142486 C G 11 GENIC homozygous 590447165 8 62142609 62142611 AG -- 9 GENIC homozygous 724102798 8 62142641 62142642 A G 13 GENIC homozygous 591782650 8 62144308 62144309 T C 10 GENIC homozygous 590447166 8 62145559 62145560 C T 5 GENIC homozygous 590447167 8 62145657 62145658 C T 6 GENIC homozygous 591782651