chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 83704238 83704239 T C 22 GENIC homozygous 986379072 15 83704349 83704350 C T 20 GENIC homozygous 986379073 15 83706015 83706016 T A 14 GENIC homozygous 986379074 15 83707219 83707220 A C 17 GENIC homozygous 986379075 15 83707313 83707314 C T 13 GENIC homozygous 986379076 15 83708662 83708663 T C 16 GENIC homozygous 986379077 15 83708714 83708715 T C 17 GENIC homozygous 986379078 15 83709425 83709426 A G 25 GENIC homozygous 986379079 15 83709428 83709429 G A 26 GENIC homozygous 986379080 15 83709599 83709600 A G 12 GENIC homozygous 986379081 15 83709928 83709929 G T 24 GENIC homozygous 986379082 15 83712565 83712566 G A 22 GENIC homozygous 986379083 15 83714778 83714779 A T 23 GENIC homozygous 986379084 15 83714812 83714813 T C 30 GENIC homozygous 986379085 15 83714911 83714912 C T 16 GENIC homozygous 986379086 15 83715044 83715045 C T 20 GENIC homozygous 986379087 15 83715242 83715243 G A 27 GENIC homozygous 986379088 15 83715357 83715358 A C 20 GENIC homozygous 986379089 15 83715864 83715865 T G 16 GENIC homozygous 986379090 15 83716250 83716251 G A 25 GENIC homozygous 986379091 15 83716306 83716307 A G 20 GENIC homozygous 986379092 15 83716753 83716754 G A 19 GENIC homozygous 986379093 15 83717520 83717521 C T 20 GENIC homozygous 986379094 15 83717854 83717855 T G 28 GENIC homozygous 986379095 15 83718033 83718034 A C 22 GENIC homozygous 986379096 15 83718655 83718656 T C 16 GENIC homozygous 986379097 15 83718699 83718700 G A 18 GENIC homozygous 986379098 15 83719267 83719268 C G 19 GENIC homozygous 986379099 15 83720299 83720300 T C 13 GENIC homozygous 986379100 15 83721061 83721062 G A 12 GENIC homozygous 986379101