chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	28260143	28260144	T	C	36	GENIC	homozygous	119023545
15	28260179	28260180	C	T	37	GENIC	heterozygous	119023546
15	28260181	28260182	G	C	38	GENIC	homozygous	119023547
15	28260318	28260319	A	G	35	GENIC	homozygous	119023548
15	28260322	28260324	CA		35	GENIC	heterozygous	131158344
15	28260324	28260325	C	T	36	GENIC	heterozygous	131166924
15	28260355	28260356	A	G	35	GENIC	heterozygous	119023549
15	28260376	28260377	G	A	26	GENIC	heterozygous	119023550
15	28260379	28260380	G	A	27	GENIC	heterozygous	119023551
15	28260385	28260386	A	T	24	GENIC	heterozygous	119023552
15	28260403	28260404	T	C	24	GENIC	homozygous	119023553
15	28260429	28260430	G	A	18	GENIC	homozygous	119023554
15	28260441	28260442	T	A	15	GENIC	heterozygous	119023555
15	28260447	28260450	CTT		15	GENIC	heterozygous	131158345
15	28260455	28260456	T	G	15	GENIC	homozygous	119023556
15	28260467	28260467		AATGATTGC	17	GENIC	heterozygous	131158346
15	28260468	28260468		CT	17	GENIC	possibly homozygous	131158347
15	28260525	28260526	T	G	24	GENIC	homozygous	119023558
15	28260871	28260872	G	A	31	GENIC	heterozygous	119023560
15	28260937	28260938	C	T	30	GENIC	heterozygous	119069694
15	28260952	28260953	A	G	28	GENIC	heterozygous	119023561
15	28260991	28260992	T	C	31	GENIC	heterozygous	119023562
15	28260996	28260997	G	A	28	GENIC	heterozygous	119023563
15	28260663	28260664	A	G	27	GENIC	homozygous	112667957