chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	116901408	116901409	C	T	20	GENIC	homozygous	136797403
3	116902182	116902183	A	G	29	GENIC	homozygous	136797404
3	116902266	116902267	A	G	25	GENIC	homozygous	136797405
3	116902912	116902913	T	G	25	GENIC	homozygous	136797406
3	116903142	116903143	C	T	25	GENIC	homozygous	136797407
3	116903841	116903842	G	A	32	GENIC	homozygous	136797408
3	116904241	116904242	T	C	26	GENIC	homozygous	136797409
3	116904246	116904247	T	C	27	GENIC	homozygous	136797410
3	116904873	116904874	G	A	36	GENIC	homozygous	136797411
3	116904944	116904945	A	G	34	GENIC	homozygous	136797412
3	116906568	116906569	C	T	41	GENIC	homozygous	136797413
3	116906773	116906773		TT	21	GENIC	homozygous	136585682
3	116908498	116908499	A	G	23	GENIC	homozygous	136797414
3	116909083	116909083		TGAT	23	GENIC	homozygous	136585683
3	116909433	116909434	T	C	16	GENIC	homozygous	136797415
3	116911349	116911350	G	A	25	GENIC	homozygous	136797416
3	116911813	116911814	C	T	35	GENIC	homozygous	136797417
3	116911822	116911823	C	G	32	GENIC	homozygous	136797418
3	116912063	116912064	A		28	GENIC	homozygous	136585684
3	116912065	116912066	G	C	29	GENIC	homozygous	136797419
3	116912115	116912116	A	G	26	GENIC	homozygous	136797420
3	116912596	116912597	C	G	27	GENIC	homozygous	136797421
3	116912942	116912943	A	G	21	GENIC	homozygous	136797422