chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	95321491	95321492	A	G	44	GENIC	homozygous	109928110
2	95322561	95322562	G	C	39	GENIC	homozygous	109928112
2	95322556	95322557	A		39	GENIC	homozygous	127654104
2	95322570	95322571	G		37	GENIC	homozygous	127654105
2	95322521	95322522	G		41	GENIC	homozygous	127654102
2	95322543	95322543		C	39	GENIC	homozygous	127654103
2	95322499	95322500	A		41	GENIC	homozygous	127654101
2	95322581	95322581		G	34	GENIC	homozygous	127654106
2	95322585	95322585		C	34	GENIC	homozygous	127654107
2	95322591	95322591		A	32	GENIC	homozygous	127654108
2	95322598	95322599	A	C	30	GENIC	homozygous	121433062
2	95322600	95322601	C	T	30	GENIC	homozygous	120350078
2	95322615	95322616	G	T	35	GENIC	homozygous	109928114
2	95322619	95322619		A	37	GENIC	homozygous	127654109
2	95322627	95322627		G	40	GENIC	homozygous	127654110
2	95322652	95322653	G		39	GENIC	homozygous	127654111
2	95322668	95322669	T		41	GENIC	homozygous	127654112
2	95322672	95322673	G	A	41	GENIC	homozygous	120251855
2	95322673	95322674	A	G	41	GENIC	homozygous	120251856
2	95322679	95322680	T	G	41	GENIC	homozygous	109928116
2	95322685	95322685		C	41	GENIC	homozygous	127654113
2	95322690	95322690		T	39	GENIC	homozygous	127654114
2	95322695	95322695		C	37	GENIC	homozygous	127654115
2	95322537	95322538	G	T	39	GENIC	homozygous	110571348
2	95322523	95322524	A	G	41	GENIC	homozygous	110571345
2	95322535	95322536	T	G	38	GENIC	homozygous	110571346