chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	21643543	21643544	T	C	52	GENIC	homozygous	141810606
6	21644591	21644592	A	C	58	GENIC	homozygous	141810607
6	21644867	21644867		G	21	GENIC	homozygous	141776110
6	21649506	21649507	T	C	79	GENIC	homozygous	141810608
6	21650699	21650700	A	G	67	GENIC	homozygous	141810609
6	21654210	21654211	T	C	55	GENIC	homozygous	141810610
6	21662584	21662585	A		36	GENIC	homozygous	137674280
6	21662620	21662621	A	C	32	GENIC	possibly homozygous	141810611
6	21662632	21662633	C	A	28	GENIC	homozygous	403168276
6	21662632	21662633	C		28	GENIC	heterozygous	403168277
6	21663531	21663532	C		15	GENIC	possibly homozygous	147741385
6	21663540	21663540		GATAAGAAAAAAGAGGGA	10	GENIC	homozygous	147741386
6	21663544	21663544		CCTCCCTCAGATAAGGGCTAACGTGAGGTACCTCACTCTGCCAATTCTTTAGATCTAGTAACAGCCTGTGGTGACTCAGGCAAAACCCAGAGGGCATCCCACACAGAGGCACTTAAACCCTTCTGCTGCTCAGGGACCCAGCTCTTAAAACACACTCACCTTTCTTGCCCTCCCATTT	7	GENIC	homozygous	147741387