chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	2504901	2504902	T	A	31	GENIC	homozygous	53765669
7	2504988	2504989	C	CTTT	17	GENIC	heterozygous	53765670
7	2505011	2505012	C	T	29	GENIC	heterozygous	54619412
7	2505756	2505757	A	G	35	GENIC	homozygous	53765671
7	2506380	2506381	T	C	35	GENIC	homozygous	54165340
7	2506480	2506482	AA	--	19	GENIC	homozygous	53765672
7	2506687	2506688	G	A	27	GENIC	homozygous	53765675
7	2506709	2506713	GTGT	----	13	GENIC	heterozygous	53765676
7	2506927	2506928	T	TGACA	33	GENIC	homozygous	53765677
7	2506928	2506929	C	G	34	GENIC	heterozygous	53765678
7	2507456	2507457	A	C	21	GENIC	homozygous	54705935
7	2508648	2508650	TT	--	15	GENIC	heterozygous	54165341
7	2508649	2508650	T	-	15	GENIC	possibly homozygous	53765681
7	2508752	2508753	G	A	44	GENIC	heterozygous	54165342
7	2509338	2509339	A	C	36	GENIC	homozygous	53765683
7	2510019	2510020	G	A	3	GENIC	heterozygous	54165343
7	2510064	2510065	T	G	11	GENIC	possibly homozygous	53765684
7	2510238	2510239	C	T	33	GENIC	homozygous	54705937
7	2510372	2510373	A	G	37	GENIC	homozygous	53765685
7	2511468	2511471	TTT	---	6	GENIC	heterozygous	53765686
7	2511469	2511471	TT	--	6	GENIC	heterozygous	53765687
7	2511487	2511488	G	T	11	GENIC	homozygous	53765688
7	2511616	2511617	T	C	22	GENIC	homozygous	53765690
7	2511636	2511637	A	-	12	GENIC	homozygous	53765693