chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 30180066 30180066 T 13 GENIC homozygous 127607275 2 30180073 30180074 C 12 GENIC homozygous 127607276 2 30180076 30180077 G A 10 GENIC homozygous 120122962 2 30180081 30180082 C T 9 GENIC homozygous 109672753 2 30180084 30180084 C 9 GENIC homozygous 127607277 2 30182001 30182001 G 11 GENIC homozygous 127607278 2 30183293 30183294 T 15 GENIC homozygous 127607279 2 30201551 30201552 C T 10 GENIC homozygous 109672829 2 30180100 30180101 C T 12 GENIC homozygous 109672755 2 30188370 30188371 A G 4 GENIC homozygous 109672775 2 30188399 30188400 C T 8 GENIC homozygous 109672777 2 30201658 30201662 CCCC 13 GENIC homozygous 127607283 2 30201663 30201663 AAT 14 GENIC homozygous 127607284 2 30213569 30213569 AGCG 15 GENIC heterozygous 129863670 2 30213575 30213576 C A 16 GENIC heterozygous 110500777 2 30213630 30213631 G A 19 GENIC heterozygous 110500779 2 30213631 30213632 G T 19 GENIC heterozygous 110500781 2 30213633 30213634 T A 19 GENIC heterozygous 110500783 2 30213652 30213653 G A 18 GENIC heterozygous 109672863 2 30213656 30213657 A G 18 GENIC heterozygous 109672865 2 30213661 30213662 C T 17 GENIC heterozygous 109672867 2 30213669 30213670 G A 17 GENIC heterozygous 109672869 2 30233786 30233854 ATGTAGCCTGGCTGTCTTGCCCAACCAGAACCTCACGCGGTTCTTGAAACTTTGGATACAGACCCTTA 12 GENIC homozygous 130244041