chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	104148247	104148248	A	T	16	GENIC	homozygous	108904619
1	104151057	104151058	C	T	26	GENIC	homozygous	109422393
1	104151563	104151564	A	G	33	GENIC	homozygous	108904630
1	104152471	104152472	C	T	25	GENIC	homozygous	109422395
1	104153703	104153704	A	G	31	GENIC	homozygous	108904635
1	104154998	104154999	A	G	25	GENIC	homozygous	109119026
1	104155006	104155007	A	G	26	GENIC	homozygous	109422397
1	104155162	104155163	C	T	9	GENIC	homozygous	109119030
1	104155182	104155183	T	G	12	GENIC	homozygous	109119032
1	104156649	104156650	A	G	22	GENIC	possibly homozygous	108904641
1	104156689	104156690	C	T	14	GENIC	homozygous	109422399
1	104157932	104157933	A	G	12	GENIC	homozygous	109422401
1	104158167	104158168	G	A	19	GENIC	homozygous	109422403
1	104158761	104158762	C	T	37	GENIC	heterozygous	109422405
1	104158776	104158777	C	T	37	GENIC	heterozygous	109422407
1	104158814	104158815	G	A	41	GENIC	heterozygous	109422409
1	104158899	104158900	G	A	23	GENIC	possibly homozygous	109422411
1	104162525	104162526	G	A	22	GENIC	homozygous	109422413
1	104163293	104163294	G	A	23	GENIC	homozygous	109422415
1	104163398	104163399	T	C	30	GENIC	homozygous	108904649
1	104165716	104165717	G	A	25	GENIC	homozygous	109422417
1	104166360	104166361	G	A	29	GENIC	homozygous	109422419