chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 31859615 31859616 A AT 3 GENIC heterozygous 723396564 12 31859766 31859767 T C 6 GENIC heterozygous 590637026 12 31859941 31859942 C T 12 GENIC possibly homozygous 591477605 12 31860519 31860520 G A 17 GENIC homozygous 591477606 12 31860632 31860633 G C 17 GENIC possibly homozygous 591477607 12 31861276 31861277 C CT 2 GENIC heterozygous 723396567 12 31862761 31862762 C T 10 GENIC possibly homozygous 591477608 12 31862905 31862906 T TA 10 GENIC homozygous 723396568 12 31863811 31863812 A G 8 GENIC homozygous 591477609 12 31863835 31863836 A T 5 GENIC homozygous 590637027 12 31863865 31863866 C G 6 GENIC homozygous 590637028 12 31864583 31864584 A G 4 GENIC heterozygous 590637029 12 31864659 31864660 T G 9 GENIC homozygous 590637030 12 31865149 31865150 A ATTT 4 GENIC homozygous 723396570 12 31865457 31865458 A G 12 GENIC homozygous 591477610 12 31865636 31865637 G A 15 GENIC possibly homozygous 591477611 12 31866057 31866058 T A 5 GENIC homozygous 590637031 12 31866269 31866271 TT -- 1 GENIC homozygous 723396571 12 31866621 31866622 C T 7 GENIC homozygous 591477612 12 31866908 31866914 AGCAGC ------ 4 GENIC homozygous 723396572 12 31867347 31867348 C T 1 GENIC homozygous 591477613 12 31867358 31867359 A AACTG 1 GENIC homozygous 723396574