chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	71938430	71938431	A	G	23	GENIC	homozygous	116051490
11	71938437	71938438	G	A	24	GENIC	homozygous	116051492
11	71938903	71938904	A	G	18	GENIC	homozygous	115985522
11	71940696	71940697	T	C	9	GENIC	homozygous	116361269
11	71941188	71941189	A	G	14	GENIC	homozygous	116051494
11	71941583	71941584	T	C	14	GENIC	homozygous	115985528
11	71941624	71941625	G	A	16	GENIC	homozygous	115985530
11	71941984	71941985	A	G	23	GENIC	homozygous	116051496
11	71942272	71942273	A	G	18	GENIC	homozygous	115985532
11	71942331	71942332	A	C	20	GENIC	homozygous	115985534
11	71942425	71942426	C	T	19	GENIC	homozygous	115985536
11	71942442	71942443	T	G	17	GENIC	homozygous	115985538
11	71942453	71942454	A	T	17	GENIC	homozygous	115985540
11	71942543	71942544	G	A	24	GENIC	homozygous	115985542
11	71945190	71945191	C	T	14	GENIC	homozygous	116267086
11	71945209	71945210	A	G	14	GENIC	homozygous	116267088
11	71946516	71946517	T	G	20	GENIC	homozygous	115985548
11	71946991	71946992	A	T	16	GENIC	homozygous	115985550
11	71942451	71942452	C		17	GENIC	homozygous	131108409
11	71940725	71940725		G	9	GENIC	homozygous	132156526
11	71947085	71947091	ACACAG		19	GENIC	homozygous	132156527
11	71942447	71942449	CA		17	GENIC	homozygous	131108408
11	71943148	71943152	CTTT		13	GENIC	homozygous	131108410
11	71945422	71945423	C	A	2	GENIC	homozygous	118163941
11	71949144	71949145	G	A	16	GENIC	homozygous	116051498
11	71950604	71950605	G	A	21	GENIC	homozygous	116051500
11	71950629	71950629		CT	20	GENIC	homozygous	132156528
11	71950642	71950643	C	A	17	GENIC	homozygous	116051502
11	71950749	71950750	G	A	29	GENIC	homozygous	116051504
11	71950993	71950994	C	T	23	GENIC	homozygous	115985558
11	71951014	71951015	C	T	24	GENIC	homozygous	116051506
11	71953010	71953010		T	16	GENIC	possibly homozygous	132156529
11	71953608	71953612	CGTA		14	GENIC	homozygous	131108412
11	71953841	71953842	C	T	15	GENIC	homozygous	116051508
11	71952355	71952356	T	G	28	GENIC	homozygous	116247737