chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	205570602	205570603	G	A	21	GENIC	homozygous	110214376
2	205571038	205571039	T	C	8	GENIC	homozygous	110214377
2	205572547	205572548	T	C	12	GENIC	homozygous	110214378
2	205575563	205575564	A	G	21	GENIC	homozygous	110214379
2	205579407	205579407		CT	8	GENIC	homozygous	127729417
2	205577341	205577461	CTCAAAACTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCCGA		10	GENIC	heterozygous	127729415
2	205579423	205579424	C		8	GENIC	homozygous	127729418
2	205579437	205579437		C	9	GENIC	homozygous	127729419
2	205579467	205579467		C	11	GENIC	homozygous	127729420
2	205579480	205579480		C	12	GENIC	homozygous	127729421
2	205579490	205579491	G		11	GENIC	homozygous	127729422
2	205581806	205581807	G	A	1	GENIC	homozygous	110214383
2	205581818	205581819	C	T	1	GENIC	homozygous	110214384
2	205583491	205583492	C	T	12	GENIC	homozygous	110214389
2	205585071	205585073	TA		3	GENIC	heterozygous	127729427
2	205585115	205585116	T	A	3	GENIC	homozygous	131321275
2	205586310	205586311	C	T	21	GENIC	homozygous	110214390
2	205588551	205588552	G	T	14	GENIC	homozygous	110214391
2	205588678	205588679	T	C	11	GENIC	homozygous	110214392
2	205589650	205589651	C	T	14	GENIC	homozygous	110214393
2	205589724	205589725	T	C	15	GENIC	homozygous	110214394