chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	116505858	116505860	TT	--	15	GENIC	heterozygous	49885221
13	116505859	116505860	T	-	15	GENIC	heterozygous	50202836
13	116505874	116505876	CC	--	19	GENIC	heterozygous	49885222
13	116518553	116518555	AA	--	2	GENIC	homozygous	49885263
13	116536801	116536802	A	-	39	GENIC	homozygous	49885306
13	116539165	116539167	GA	--	4	GENIC	heterozygous	50378823
13	116540949	116540951	TA	--	5	GENIC	heterozygous	49885317
13	116540949	116540950	T	TGTGTTTTATGTATATGTATGAGC	6	GENIC	heterozygous	49885318
13	116540955	116540956	T	-	8	GENIC	heterozygous	49885319
13	116540982	116540983	G	A	12	GENIC	heterozygous	49885320
13	116540993	116540994	G	A	12	GENIC	heterozygous	49885321
13	116541001	116541002	G	A	10	GENIC	heterozygous	49885322
13	116541010	116541011	G	C	8	GENIC	heterozygous	49885323
13	116541025	116541028	TGT	---	10	GENIC	homozygous	49885324
13	116541027	116541028	T	TG	10	GENIC	heterozygous	49885325
13	116541039	116541041	TG	--	9	GENIC	heterozygous	49885326
13	116541046	116541047	G	-	9	GENIC	heterozygous	49885327
13	116541048	116541049	A	-	10	GENIC	heterozygous	49885328
13	116541053	116541054	A	G	11	GENIC	heterozygous	49885329
13	116541062	116541063	G	T	10	GENIC	homozygous	49885330
13	116541077	116541078	T	G	12	GENIC	possibly homozygous	49885332
13	116541107	116541108	G	T	21	GENIC	homozygous	49885333
13	116541124	116541125	G	T	20	GENIC	homozygous	49885334
13	116541126	116541127	G	T	20	GENIC	homozygous	49885335
13	116541142	116541143	G	T	24	GENIC	homozygous	49885336
13	116541146	116541147	G	T	24	GENIC	homozygous	49885337
13	116546232	116546233	A	T	23	GENIC	possibly homozygous	50378825
13	116547080	116547081	C	A	10	GENIC	heterozygous	49885357
13	116551685	116551686	C	CT	26	GENIC	homozygous	49885374
13	116551747	116551748	G	-	24	GENIC	homozygous	49885375