chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	17252750	17252751	A	C	25	GENIC	homozygous	115273343
12	17252845	17252846	A	G	33	GENIC	homozygous	115273345
12	17253230	17253231	A	C	25	GENIC	homozygous	115273347
12	17253406	17253407	T	G	19	GENIC	homozygous	115273349
12	17253437	17253438	T	C	20	GENIC	homozygous	115273351
12	17254195	17254196	G	A	31	GENIC	homozygous	115273353
12	17254378	17254379	C	G	22	GENIC	homozygous	115273355
12	17255333	17255334	A	G	19	GENIC	homozygous	115273357
12	17256749	17256750	G	A	20	GENIC	homozygous	115273359
12	17257163	17257164	G	T	24	GENIC	homozygous	115273361
12	17257622	17257623	A	G	14	GENIC	homozygous	115273363
12	17257756	17257757	G	A	14	GENIC	homozygous	115273365
12	17258204	17258205	C	A	9	GENIC	homozygous	115421323
12	17258345	17258346	A	T	25	GENIC	homozygous	115273367
12	17258547	17258548	G	A	29	GENIC	homozygous	115273369
12	17258611	17258612	A	G	16	GENIC	homozygous	115273371
12	17258825	17258826	T	C	13	GENIC	homozygous	115364971
12	17258911	17258912	C	T	16	GENIC	homozygous	115273373
12	17259943	17259944	G	A	15	GENIC	homozygous	115273375
12	17260056	17260057	G	A	18	GENIC	homozygous	115273377
12	17260759	17260760	A	G	25	GENIC	homozygous	115273379
12	17262013	17262014	T	C	28	GENIC	homozygous	115273383