chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 110452397 110452398 C T 21 GENIC homozygous 957594237 3 110454715 110454716 A G 33 GENIC homozygous 957594238 3 110462720 110462721 G A 19 GENIC homozygous 957594239 3 110463051 110463052 G A 21 GENIC homozygous 957594240 3 110463066 110463067 A G 22 GENIC homozygous 957594241 3 110465091 110465092 T C 17 GENIC homozygous 957594242 3 110465447 110465448 A G 35 GENIC homozygous 957594243 3 110466543 110466544 C T 9 GENIC homozygous 957594244 3 110467748 110467749 G C 21 GENIC homozygous 957594245 3 110469248 110469249 T C 20 GENIC homozygous 957594246 3 110469574 110469575 A G 18 GENIC homozygous 957594247 3 110474429 110474430 T G 27 GENIC homozygous 957594248 3 110475728 110475729 T C 33 GENIC homozygous 957594249 3 110476491 110476492 G A 25 GENIC homozygous 957594250 3 110480114 110480115 G T 21 GENIC homozygous 957594251 3 110481041 110481042 G A 27 GENIC homozygous 957594252 3 110481403 110481404 T C 26 GENIC homozygous 957594253 3 110481916 110481917 C T 27 GENIC homozygous 957594254 3 110482841 110482842 A G 44 GENIC homozygous 957594255 3 110485820 110485821 C T 25 GENIC homozygous 957594256