chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	187114527	187114528	A	G	17	GENIC	homozygous	110166929
2	187114784	187114785	T	C	24	GENIC	homozygous	110166930
2	187114917	187114918	A	G	23	GENIC	homozygous	110166931
2	187115561	187115562	A	G	17	GENIC	homozygous	110166932
2	187116861	187116862	A	G	18	GENIC	homozygous	110166933
2	187121209	187121210	A	G	22	GENIC	homozygous	110166937
2	187121900	187121901	A	G	24	GENIC	homozygous	110166938
2	187125163	187125164	C	T	14	GENIC	homozygous	110166943
2	187126341	187126342	G	A	13	GENIC	homozygous	110166944
2	187127537	187127538	G	A	13	GENIC	homozygous	110166945
2	187128724	187128725	G	T	11	GENIC	homozygous	111278030
2	187115916	187115919	AAG		12	GENIC	homozygous	130873681
2	187120120	187120120		G	15	GENIC	homozygous	130873682
2	187123006	187123006		AT	12	GENIC	heterozygous	130873683
2	187115972	187115973	G	A	17	GENIC	homozygous	111278025
2	187117714	187117715	G	A	19	GENIC	homozygous	111278026
2	187125325	187125326	C	T	16	GENIC	homozygous	111278028
2	187123008	187123009	T	A	12	GENIC	heterozygous	130896114
2	187129351	187129351		TC	11	GENIC	possibly homozygous	130740998
2	187129762	187129763	C	T	21	GENIC	homozygous	110166947
2	187130331	187130332	G	A	14	GENIC	homozygous	110166948
2	187131387	187131387		CTTT	23	GENIC	homozygous	130873685
2	187133520	187133521	C	T	22	GENIC	possibly homozygous	111278032