chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	97177851	97177852	T	C	14	GENIC	homozygous	109937787
2	97178560	97178561	C	G	9	GENIC	homozygous	109937795
2	97186746	97186747	A	C	28	GENIC	homozygous	110573904
2	97186819	97186820	C	A	26	GENIC	homozygous	109937811
2	97187962	97187963	C	T	17	GENIC	homozygous	109937824
2	97190815	97190816	T	A	11	GENIC	homozygous	110573909
2	97191868	97191869	C	G	24	GENIC	homozygous	109937856
2	97192201	97192202	G	C	21	GENIC	homozygous	110573911
2	97195048	97195049	T	G	33	GENIC	homozygous	110573917
2	97195756	97195757	T	G	15	GENIC	homozygous	110573919
2	97195882	97195883	G	A	16	GENIC	homozygous	109937876
2	97196222	97196223	C	T	30	GENIC	homozygous	110573920
2	97196464	97196465	C	G	17	GENIC	homozygous	110573922
2	97196653	97196654	T	A	17	GENIC	homozygous	110573924
2	97198349	97198350	A	C	24	GENIC	homozygous	110573936
2	97199411	97199412	A	T	18	GENIC	homozygous	109937903
2	97199549	97199550	T	G	18	GENIC	possibly homozygous	109937905
2	97199553	97199554	C	T	20	GENIC	homozygous	110573940
2	97199554	97199555	C	T	20	GENIC	homozygous	110573942