chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 148234690 148234691 T C 23 GENIC homozygous 111769076 3 148234991 148234992 C T 18 GENIC homozygous 111769078 3 148238151 148238152 C T 18 GENIC homozygous 111769080 3 148239106 148239107 G A 23 GENIC possibly homozygous 111769082 3 148239828 148239829 T G 28 GENIC homozygous 111769084 3 148240119 148240120 C T 23 GENIC homozygous 111769086 3 148240197 148240198 T A 14 GENIC homozygous 111769088 3 148240878 148240879 G A 16 GENIC homozygous 111769092 3 148241050 148241051 T C 29 GENIC homozygous 111769094 3 148241501 148241502 G A 23 GENIC homozygous 111769096 3 148240031 148240032 C 26 GENIC homozygous 127940835 3 148241707 148241708 T 13 GENIC homozygous 127940837 3 148238303 148238303 CCTCCCTCCCCTTCTC 20 GENIC homozygous 127940833 3 148239679 148239679 A 25 GENIC homozygous 127940834 3 148240798 148240806 AAACAAAC 18 GENIC homozygous 127940836 3 148242127 148242128 G A 28 GENIC homozygous 111769098 3 148243472 148243473 C T 28 GENIC homozygous 111769100 3 148243881 148243881 G 21 GENIC homozygous 127940838 3 148244495 148244496 A T 20 GENIC possibly homozygous 111769102 3 148244506 148244507 C G 22 GENIC homozygous 111769104