chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	95084762	95084763	C	T	26	GENIC	homozygous	110721654
2	95087244	95087245	T	G	21	GENIC	homozygous	109927115
2	95087675	95087676	G	A	17	GENIC	homozygous	110721655
2	95088503	95088504	C	T	23	GENIC	homozygous	110721656
2	95088889	95088890	T	C	18	GENIC	homozygous	109927123
2	95089222	95089223	C	T	28	GENIC	homozygous	110721657
2	95089255	95089256	T	G	23	GENIC	homozygous	109927125
2	95090753	95090754	T	C	28	GENIC	homozygous	109927131
2	95090783	95090784	C	A	26	GENIC	homozygous	110721660
2	95090831	95090832	C	T	20	GENIC	homozygous	110721661
2	95090880	95090881	C	T	32	GENIC	homozygous	109927133
2	95092824	95092825	A	C	22	GENIC	homozygous	109927141
2	95093674	95093675	C	A	29	GENIC	homozygous	110721662
2	95097867	95097868	T	C	26	GENIC	homozygous	109927157
2	95097871	95097872	C	T	27	GENIC	homozygous	109927159
2	95098304	95098305	T	A	20	GENIC	homozygous	110721664
2	95100271	95100272	G	A	20	GENIC	homozygous	109927173
2	95100342	95100343	C	T	30	GENIC	homozygous	110721665
2	95100450	95100451	C	T	31	GENIC	homozygous	110721666
2	95102103	95102104	A	G	23	GENIC	homozygous	109927177
2	95102965	95102966	G	A	35	GENIC	homozygous	110721668
2	95104543	95104544	C	T	22	GENIC	homozygous	109927183
2	95104546	95104547	C	T	22	GENIC	homozygous	109927185
2	95104597	95104598	C	A	23	GENIC	homozygous	110721669
2	95104940	95104941	G	C	44	GENIC	homozygous	110721670
2	95104988	95104989	T	C	34	GENIC	homozygous	109927187
2	95106011	95106012	T	C	25	GENIC	homozygous	110721671
2	95106124	95106125	C	T	35	GENIC	homozygous	110721672