chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 103657968 103657969 A G 16 GENIC homozygous 650046414 10 103658439 103658440 A G 21 GENIC homozygous 650046415 10 103658665 103658666 C T 14 GENIC homozygous 650046416 10 103659475 103659476 A C 22 GENIC homozygous 650046417 10 103662334 103662335 C - 4 GENIC heterozygous 757147169 10 103662601 103662602 C CT 16 GENIC heterozygous 757147170 10 103662715 103662719 TTTT ---- 9 GENIC heterozygous 757147171 10 103665767 103665768 A G 21 GENIC homozygous 650046418 10 103667623 103667624 C T 21 GENIC homozygous 650046419 10 103667793 103667794 A G 28 GENIC homozygous 650046420 10 103667854 103667855 A G 21 GENIC homozygous 650046421 10 103668206 103668210 GTGT ---- 15 GENIC homozygous 757147173 10 103668541 103668543 AA -- 13 GENIC possibly homozygous 757147174 10 103669968 103669969 C T 28 GENIC homozygous 650046422 10 103670372 103670373 C T 20 GENIC homozygous 650046423