chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	31098924	31098925	T	A	22	GENIC	homozygous	110321893
18	31099243	31099244	A	T	18	GENIC	homozygous	110321896
18	31099406	31099407	A	C	26	GENIC	homozygous	110532859
18	31099813	31099814	T	A	34	GENIC	homozygous	110532861
18	31100611	31100612	A	G	27	GENIC	homozygous	110321900
18	31101322	31101323	A	G	36	GENIC	homozygous	110532863
18	31101327	31101328	T	C	38	GENIC	homozygous	110532865
18	31101443	31101444	T	C	19	GENIC	possibly homozygous	110532867
18	31102345	31102346	T	C	6	GENIC	homozygous	110532869
18	31102713	31102714	C	T	3	GENIC	homozygous	110532872
18	31103069	31103070	G	A	11	GENIC	homozygous	110532874
18	31103171	31103172	A	T	21	GENIC	homozygous	110532876
18	31103503	31103504	G	A	10	GENIC	homozygous	110532878
18	31103720	31103721	C	A	15	GENIC	homozygous	110532880
18	31104231	31104232	G	A	18	GENIC	homozygous	110532882
18	31104249	31104250	T	C	20	GENIC	homozygous	110321904
18	31104394	31104395	T	C	32	GENIC	homozygous	110532884
18	31104493	31104494	C	A	20	GENIC	homozygous	110532886
18	31104863	31104864	T	C	23	GENIC	homozygous	110321906
18	31106746	31106747	C	T	29	GENIC	homozygous	110532888
18	31106962	31106963	G	A	14	GENIC	possibly homozygous	110532890
18	31108699	31108700	C	T	10	GENIC	homozygous	110859044
18	31108871	31108872	C	T	7	GENIC	homozygous	110457586