chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 42711201 42711202 C - 29 GENIC homozygous 49307377 14 42711204 42711205 C CA 27 GENIC homozygous 49307378 14 42711383 42711384 A G 29 GENIC possibly homozygous 48685119 14 42711501 42711502 T C 21 GENIC homozygous 48685120 14 42711753 42711754 T TAC 2 GENIC homozygous 49396705 14 42712304 42712305 A G 21 GENIC homozygous 49178650 14 42712735 42712736 C A 31 GENIC homozygous 48685122 14 42712839 42712840 T C 29 GENIC homozygous 48685123 14 42713594 42713595 T C 27 GENIC homozygous 49178651 14 42713714 42713715 A G 27 GENIC homozygous 48685125 14 42713870 42713871 T TA 21 GENIC homozygous 49178652 14 42714470 42714471 A G 29 GENIC homozygous 48685127 14 42716112 42716115 GGG --- 15 GENIC homozygous 49178653 14 42716157 42716158 C T 15 GENIC homozygous 49178654 14 42716180 42716181 T C 17 GENIC homozygous 48685131 14 42716826 42716827 A - 19 GENIC homozygous 49178655 14 42716882 42716883 C A 27 GENIC homozygous 49178656 14 42716947 42716948 G A 21 GENIC homozygous 49178657 14 42717412 42717413 T C 32 GENIC homozygous 48685133 14 42718587 42718588 T A 27 GENIC homozygous 49178658