chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39165486	39165487	G	A	21	GENIC	homozygous	115324940
12	39166151	39166152	G	T	10	GENIC	homozygous	118270173
12	39166697	39166698	C	A	24	GENIC	homozygous	115324942
12	39167157	39167158	A	G	19	GENIC	homozygous	115324944
12	39167766	39167767	G	A	19	GENIC	homozygous	115324946
12	39168021	39168022	A	G	4	GENIC	heterozygous	115476849
12	39168302	39168303	G	A	18	GENIC	homozygous	115324948
12	39168842	39168843	G	T	6	GENIC	heterozygous	126224575
12	39169442	39169443	G	A	13	GENIC	homozygous	115324952
12	39170645	39170646	G	A	19	GENIC	homozygous	115324954
12	39170858	39170859	G	A	16	GENIC	homozygous	115324956
12	39171743	39171744	G	A	8	GENIC	homozygous	115324958
12	39171744	39171745	A	C	7	GENIC	homozygous	115324960
12	39171745	39171746	G	A	7	GENIC	homozygous	115324962
12	39172641	39172642	C	T	28	GENIC	homozygous	115324970
12	39174227	39174228	A	T	5	GENIC	homozygous	126224576
12	39174689	39174690	G	A	4	GENIC	homozygous	126224577
12	39175287	39175288	G	A	15	GENIC	homozygous	118270180
12	39177100	39177101	T	G	21	GENIC	homozygous	126173264
12	39179755	39179756	A	G	30	GENIC	homozygous	126173265
12	39180400	39180401	A	C	30	GENIC	possibly homozygous	126173266
12	39182405	39182406	G	A	23	GENIC	homozygous	126173267
12	39183321	39183322	C	G	6	GENIC	heterozygous	115324972
12	39183928	39183929	T	A	5	GENIC	homozygous	126173268