chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	52452237	52452238	T	C	17	GENIC	homozygous	109754116
2	52456297	52456298	G	A	25	GENIC	homozygous	109754119
2	52457035	52457036	T	C	23	GENIC	homozygous	109754121
2	52459707	52459708	C	T	24	GENIC	homozygous	110932468
2	52463724	52463725	G	T	30	GENIC	homozygous	110932473
2	52464705	52464706	C	T	12	GENIC	homozygous	110932474
2	52468246	52468247	G	A	28	GENIC	homozygous	110932475
2	52470693	52470694	T	C	19	GENIC	homozygous	109754161
2	52477802	52477803	G	A	12	GENIC	homozygous	110932477
2	52480039	52480040	T	C	12	GENIC	homozygous	109754205
2	52480451	52480452	T	C	19	GENIC	homozygous	109754208
2	52487374	52487375	G	A	10	GENIC	homozygous	109754235
2	52487434	52487435	G	A	21	GENIC	homozygous	110522404
2	52487480	52487481	A	G	18	GENIC	homozygous	109754239
2	52487541	52487542	C	G	9	GENIC	homozygous	109754240
2	52489715	52489716	C	T	17	GENIC	homozygous	110932479
2	52491426	52491427	G	A	11	GENIC	homozygous	110932480
2	52491718	52491719	A	T	20	GENIC	homozygous	109754260
2	52491725	52491726	G	C	18	GENIC	homozygous	109754261
2	52491735	52491736	G	C	19	GENIC	homozygous	109754262
2	52491740	52491741	A	G	19	GENIC	homozygous	109754263
2	52491742	52491743	A	T	20	GENIC	homozygous	109754264
2	52491745	52491746	A	C	20	GENIC	homozygous	109754265