chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 105019257 105019258 G A 26 GENIC homozygous 951703561 2 105019258 105019259 A G 26 GENIC homozygous 951703562 2 105019284 105019285 A C 27 GENIC homozygous 951703563 2 105027043 105027044 A G 19 GENIC homozygous 951703564 2 105027084 105027085 C G 20 GENIC homozygous 951703565 2 105028519 105028520 C T 19 GENIC homozygous 951703566 2 105029318 105029319 C A 27 GENIC homozygous 951703567 2 105029712 105029713 T C 37 GENIC homozygous 951703568 2 105033447 105033448 G T 25 GENIC homozygous 951703569 2 105033724 105033725 G A 24 GENIC homozygous 951703570 2 105038403 105038404 T A 19 GENIC homozygous 951703571 2 105044760 105044761 A T 29 GENIC homozygous 951703572 2 105045764 105045765 T G 14 GENIC homozygous 951703573