chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	39991870	39991871	A	C	7	GENIC	heterozygous	113023776
15	40059741	40059742	T	C	12	GENIC	homozygous	112485150
15	40062579	40062580	C	G	15	GENIC	homozygous	113000570
15	40073493	40073494	G	T	20	GENIC	homozygous	112485166
15	40073586	40073587	A	G	21	GENIC	homozygous	112851923
15	40073800	40073801	A	G	29	GENIC	homozygous	112485168
15	40073842	40073843	C	G	29	GENIC	homozygous	112672842
15	40074224	40074225	A	T	18	GENIC	homozygous	112879251
15	40091308	40091309	G	A	17	GENIC	heterozygous	113023778
15	40116266	40116267	G	A	35	GENIC	homozygous	112485329
15	40192392	40192393	C	G	17	GENIC	homozygous	112672846
15	40192393	40192394	G	C	18	GENIC	homozygous	112672848
15	40230932	40230933	A	G	32	GENIC	homozygous	112485913
15	40230933	40230934	C	A	32	GENIC	homozygous	112485915
15	40230941	40230942	C	A	28	GENIC	homozygous	112485918
15	40353695	40353696	G	C	10	GENIC	homozygous	112486652
15	40353709	40353710	G	A	8	GENIC	homozygous	112486654
15	40414549	40414550	G	T	27	GENIC	homozygous	112486893
15	40414603	40414604	C	A	22	GENIC	homozygous	112486895
15	40418208	40418209	G	C	10	GENIC	homozygous	112808302
15	40424796	40424797	T	A	22	GENIC	homozygous	112487033
15	40451937	40451938	T	C	23	GENIC	homozygous	112808326
15	40451938	40451939	C	G	24	GENIC	homozygous	112808328
15	40472008	40472009	G	A	35	GENIC	heterozygous	112988152