chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	156342575	156342576	C	T	28	GENIC	heterozygous	110074079
2	156342743	156342744	G	A	29	GENIC	possibly homozygous	110074081
2	156345410	156345411	A	G	10	GENIC	heterozygous	110074084
2	156345647	156345648	C	G	29	GENIC	heterozygous	110772813
2	156345663	156345664	C	T	25	GENIC	heterozygous	111270430
2	156345745	156345746	C	A	24	GENIC	heterozygous	111270432
2	156345757	156345758	C	T	23	GENIC	heterozygous	111270434
2	156345789	156345790	T	C	17	GENIC	heterozygous	111270435
2	156350922	156350923	T	A	14	GENIC	possibly homozygous	110074087
2	156370355	156370356	G	C	31	GENIC	heterozygous	110601329
2	156404582	156404583	C	T	16	GENIC	possibly homozygous	110074094
2	156423959	156423960	C	T	60	GENIC	heterozygous	110601333
2	156423968	156423969	A	G	62	GENIC	heterozygous	110074095
2	156423973	156423974	A	G	68	GENIC	heterozygous	110074096
2	156424041	156424042	C	T	76	GENIC	heterozygous	110074098
2	156424058	156424059	C	T	70	GENIC	heterozygous	110074099
2	156424102	156424103	T	C	62	GENIC	heterozygous	110074100
2	156424133	156424134	A	G	67	GENIC	heterozygous	110074101
2	156424143	156424144	G	A	63	GENIC	heterozygous	110074102
2	156424162	156424163	T	C	86	GENIC	heterozygous	110074103
2	156424176	156424177	T	G	91	GENIC	heterozygous	110074104
2	156424267	156424268	A	G	84	GENIC	heterozygous	111270437