chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	97177851	97177852	T	C	23	GENIC	homozygous	109937787
2	97178560	97178561	C	G	17	GENIC	homozygous	109937795
2	97186746	97186747	A	C	30	GENIC	homozygous	110573904
2	97186819	97186820	C	A	34	GENIC	homozygous	109937811
2	97187962	97187963	C	T	32	GENIC	homozygous	109937824
2	97191868	97191869	C	G	14	GENIC	homozygous	109937856
2	97192201	97192202	G	C	15	GENIC	homozygous	110573911
2	97195048	97195049	T	G	24	GENIC	homozygous	110573917
2	97195756	97195757	T	G	27	GENIC	homozygous	110573919
2	97195882	97195883	G	A	31	GENIC	homozygous	109937876
2	97196222	97196223	C	T	26	GENIC	homozygous	110573920
2	97196464	97196465	C	G	25	GENIC	homozygous	110573922
2	97196653	97196654	T	A	30	GENIC	homozygous	110573924
2	97198349	97198350	A	C	29	GENIC	homozygous	110573936
2	97198453	97198454	T	A	7	GENIC	homozygous	110573938
2	97199411	97199412	A	T	23	GENIC	homozygous	109937903