chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	243703066	243703067	C	T	35	GENIC	homozygous	60087636
2	243703891	243703892	A	G	21	GENIC	homozygous	59472311
2	243703899	243703900	G	A	23	GENIC	homozygous	60087637
2	243704224	243704227	TTG	---	3	GENIC	heterozygous	59472312
2	243704231	243704232	G	T	8	GENIC	heterozygous	59950389
2	243704413	243704414	A	C	11	GENIC	heterozygous	59472313
2	243704457	243704458	A	AC	6	GENIC	heterozygous	60087638
2	243704677	243704678	G	A	37	GENIC	possibly homozygous	59472315
2	243705298	243705299	T	TA	5	GENIC	homozygous	59472321
2	243706074	243706075	A	G	34	GENIC	homozygous	59472322
2	243706468	243706469	A	G	18	GENIC	homozygous	59472323
2	243707930	243707931	T	C	21	GENIC	homozygous	59472326
2	243708087	243708088	G	C	21	GENIC	homozygous	59472327
2	243709284	243709288	CTCT	----	13	GENIC	possibly homozygous	60087639
2	243713323	243713324	C	-	23	GENIC	homozygous	59472333
2	243713389	243713390	C	-	29	GENIC	homozygous	59472334
2	243717471	243717472	G	-	11	GENIC	heterozygous	59472342