chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 41315793 41315794 A ATG 38 GENIC heterozygous 736141656 10 41315973 41315974 A - 12 GENIC homozygous 736141657 10 41315975 41315976 C - 12 GENIC homozygous 736141658 10 41315978 41315979 T - 11 GENIC homozygous 736141659 10 41315985 41315986 T - 22 GENIC heterozygous 736141660 10 41316237 41316238 A C 35 GENIC homozygous 615966545 10 41316387 41316388 A - 52 GENIC heterozygous 736141661 10 41316395 41316396 G T 55 GENIC heterozygous 615966546 10 41316432 41316433 G A 44 GENIC homozygous 614010375 10 41316443 41316444 A C 36 GENIC homozygous 614010376 10 41316451 41316452 T C 31 GENIC homozygous 615966547 10 41316482 41316483 T A 35 GENIC homozygous 615966548 10 41316497 41316498 G C 37 GENIC homozygous 615966549 10 41316624 41316625 C CAG 20 GENIC homozygous 736141662 10 41316652 41316653 A G 24 GENIC homozygous 614010377 10 41316709 41316710 A - 21 GENIC possibly homozygous 736141663 10 41316713 41316716 GGG --- 31 GENIC heterozygous 736141664 10 41316781 41316782 T G 19 GENIC homozygous 615966550 10 41316787 41316789 TC -- 20 GENIC possibly homozygous 736141665 10 41316830 41316833 GGG --- 42 GENIC heterozygous 736141666 10 41316831 41316834 GGT --- 42 GENIC heterozygous 736141668 10 41316834 41316835 G GCA 42 GENIC heterozygous 736141669 10 41316933 41316934 C G 47 GENIC heterozygous 615966551 10 41317021 41317022 G T 70 GENIC heterozygous 614010378 10 41317094 41317095 C T 21 GENIC homozygous 614010379 10 41317157 41317158 A - 56 GENIC heterozygous 736141672 10 41317173 41317174 T TG 43 GENIC heterozygous 736141673 10 41317214 41317215 C T 41 GENIC heterozygous 615966552 10 41317215 41317216 C G 41 GENIC heterozygous 615966553 10 41317282 41317283 A T 50 GENIC heterozygous 614010380