chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	274717305	274717306	A	T	12	GENIC	homozygous	61227617
1	274717506	274717507	C	T	28	GENIC	homozygous	61227618
1	274719239	274719240	C	CCCTT	11	GENIC	homozygous	61334741
1	274719834	274719835	C	CTG	19	GENIC	homozygous	61227621
1	274721167	274721168	T	C	18	GENIC	homozygous	61227622
1	274722252	274722253	A	AGG	15	GENIC	homozygous	61227623
1	274727064	274727065	G	A	16	GENIC	homozygous	61227625
1	274727487	274727488	A	T	21	GENIC	homozygous	61227626
1	274729661	274729662	T	C	10	GENIC	homozygous	61647490
1	274732141	274732142	C	T	8	GENIC	homozygous	61647494
1	274732804	274732805	A	G	16	GENIC	homozygous	61227635
1	274733423	274733424	A	T	24	GENIC	homozygous	61227637
1	274734305	274734306	C	A	11	GENIC	homozygous	61334751
1	274734306	274734307	A	G	11	GENIC	homozygous	61334752
1	274736378	274736379	G	A	22	GENIC	homozygous	61647496
1	274737372	274737373	A	G	20	GENIC	homozygous	61227647
1	274737703	274737704	T	A	14	GENIC	homozygous	61227650
1	274738889	274738890	T	C	14	GENIC	homozygous	61227653
1	274740143	274740144	C	CGTCCTTCCTG	14	GENIC	homozygous	61227659
1	274740996	274740997	T	-	11	GENIC	homozygous	61647497
1	274741019	274741020	T	G	13	GENIC	homozygous	61227674
1	274742050	274742051	C	T	16	GENIC	homozygous	61647498
1	274743726	274743727	T	C	21	GENIC	homozygous	61227702
1	274744056	274744057	G	T	24	GENIC	homozygous	61334765
1	274744113	274744114	G	A	13	GENIC	homozygous	61647499
1	274744122	274744123	A	-	11	GENIC	homozygous	61647500
1	274744143	274744144	G	A	12	GENIC	homozygous	61647501
1	274744250	274744251	A	G	12	GENIC	homozygous	62112790
1	274746550	274746551	T	C	21	GENIC	homozygous	61227705
1	274739782	274739786	AAAT	----	7	GENIC	homozygous	62816841
1	274722632	274722633	C	T	14	GENIC	homozygous	61972364
1	274744206	274744207	A	AG	10	GENIC	homozygous	61972366
1	274735965	274735973	ACACACAC	--------	6	GENIC	homozygous	62816840