chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 122702184 122702185 C T 49 GENIC homozygous 115861157 7 122702545 122702546 G A 36 GENIC homozygous 115861161 7 122702664 122702665 A T 17 GENIC homozygous 115861163 7 122702705 122702707 CA 7 GENIC homozygous 128513535 7 122702703 122702703 A 7 GENIC homozygous 128513534 7 122702648 122702649 C 21 GENIC homozygous 128513531 7 122702679 122702680 T 9 GENIC homozygous 128513532 7 122702681 122702682 T 9 GENIC homozygous 128513533 7 122702649 122702650 A G 21 GENIC homozygous 118322360 7 122702722 122702723 G 4 GENIC homozygous 128513536 7 122702725 122702726 A 4 GENIC homozygous 128513537 7 122703155 122703158 GGC 5 GENIC homozygous 128513538 7 122703161 122703162 A 5 GENIC homozygous 128513539 7 122703171 122703173 CG 5 GENIC homozygous 128513540 7 122703199 122703199 A 15 GENIC homozygous 128513541 7 122703202 122703202 AA 16 GENIC homozygous 128513542 7 122703557 122703558 C T 29 GENIC homozygous 115861170 7 122707502 122707503 C T 50 GENIC homozygous 118322362 7 122703781 122703782 T C 25 GENIC possibly homozygous 118512451 7 122709097 122709097 GGGGA 13 GENIC homozygous 128513545 7 122709101 122709101 GC 13 GENIC homozygous 128513546 7 122709102 122709102 CAGTGGTAGAGCGCTTGCCTAGCAAGCA 13 GENIC homozygous 128513547 7 122710110 122710111 C 34 GENIC homozygous 128513548 7 122710164 122710165 A C 43 GENIC homozygous 115861180 7 122710213 122710213 T 43 GENIC homozygous 128513549 7 122710220 122710221 T 41 GENIC homozygous 128513550 7 122710278 122710279 C 42 GENIC homozygous 128513551 7 122710335 122710336 A 46 GENIC homozygous 128513552 7 122710377 122710378 G 44 GENIC homozygous 128513553 7 122710861 122710864 ATT 40 GENIC homozygous 131024279