chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	49457551	49457552	A	C	12	GENIC	homozygous	109723642
19	49459577	49459578	A	G	31	GENIC	homozygous	109723644
19	49459803	49459804	T	G	33	GENIC	homozygous	109723646
19	49460801	49460802	T	C	22	GENIC	homozygous	109723648
19	49460961	49460962	A	G	22	GENIC	homozygous	109723650
19	49461383	49461384	C	T	14	GENIC	homozygous	109723651
19	49461835	49461836	C	T	25	GENIC	homozygous	109723653
19	49462589	49462590	G	A	32	GENIC	homozygous	109723655
19	49463484	49463485	T	A	21	GENIC	homozygous	109723657
19	49463496	49463497	C	T	22	GENIC	homozygous	109723659
19	49464304	49464305	G	A	27	GENIC	homozygous	109723661
19	49464530	49464531	G	A	15	GENIC	homozygous	109723663
19	49465146	49465147	G	A	23	GENIC	homozygous	109723665
19	49465254	49465255	G	C	30	GENIC	homozygous	109723667
19	49465479	49465480	C	T	22	GENIC	homozygous	109723669
19	49465857	49465858	C	A	22	GENIC	homozygous	109723671
19	49466417	49466418	C	G	24	GENIC	homozygous	109723673
19	49466486	49466487	T	C	14	GENIC	homozygous	109723675
19	49466529	49466530	A	C	11	GENIC	homozygous	109723677
19	49467470	49467471	T	G	25	GENIC	homozygous	109723679
19	49471301	49471302	T	A	17	GENIC	homozygous	109723681
19	49471372	49471373	G	A	18	GENIC	homozygous	109723683
19	49472490	49472491	A	G	35	GENIC	homozygous	109723685
19	49472508	49472509	T	C	36	GENIC	homozygous	109723687
19	49472839	49472840	T	G	29	GENIC	homozygous	109723689
19	49474710	49474711	G	A	28	GENIC	homozygous	109723691
19	49474973	49474974	C	T	19	GENIC	homozygous	109723693
19	49476978	49476979	A	G	26	GENIC	homozygous	109723695
19	49477725	49477726	G	A	28	GENIC	homozygous	109723697
19	49477843	49477844	T	C	23	GENIC	homozygous	109723699
19	49478615	49478616	A	G	15	GENIC	homozygous	109723701
19	49479139	49479140	C	T	29	GENIC	homozygous	109723703