chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	35196079	35196080	C	CA	4	GENIC	homozygous	55141221
7	35197106	35197107	A	-	15	GENIC	heterozygous	54562795
7	35197293	35197297	GAAA	----	14	GENIC	homozygous	54968023
7	35197297	35197298	C	CCCCA	13	GENIC	homozygous	54968025
7	35197298	35197299	G	T	14	GENIC	homozygous	54968027
7	35197925	35197926	T	-	16	GENIC	homozygous	53871315
7	35197928	35197929	A	-	16	GENIC	homozygous	53871316
7	35197932	35197933	A	-	15	GENIC	homozygous	53871317
7	35197943	35197944	T	-	14	GENIC	homozygous	53871318
7	35197944	35197945	T	G	13	GENIC	homozygous	54968029
7	35197947	35197948	T	-	13	GENIC	homozygous	53871319
7	35197953	35197954	T	-	13	GENIC	homozygous	53871320
7	35197957	35197958	T	-	13	GENIC	homozygous	53871321
7	35198229	35198232	AAG	---	18	GENIC	heterozygous	54191502
7	35205146	35205147	C	CTCCCTCCG	10	GENIC	homozygous	54968039
7	35215620	35215621	T	C	10	GENIC	homozygous	53871324
7	35216038	35216039	G	T	4	GENIC	homozygous	53871329
7	35216072	35216073	A	G	15	GENIC	homozygous	53871330
7	35216122	35216123	A	G	16	GENIC	homozygous	53871331
7	35216754	35216755	G	A	24	GENIC	homozygous	53871333
7	35216788	35216789	C	CA	28	GENIC	homozygous	53871334
7	35219053	35219054	G	A	10	GENIC	homozygous	53871335
7	35219070	35219073	TTT	---	10	GENIC	homozygous	53871336
7	35225284	35225293	TGTCCTGCC	---------	8	GENIC	possibly homozygous	55621279