chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 153732871 153732872 C T 20 GENIC homozygous 108314037 1 153733082 153733083 T A 39 GENIC homozygous 108314039 1 153734772 153734773 T C 22 GENIC homozygous 108314041 1 153734838 153734839 A G 16 GENIC homozygous 108314043 1 153735543 153735544 T C 31 GENIC homozygous 108314045 1 153736357 153736358 A G 29 GENIC homozygous 108314047 1 153736402 153736403 T C 34 GENIC homozygous 108314049 1 153736674 153736675 C T 23 GENIC homozygous 108314051 1 153736727 153736728 C T 32 GENIC homozygous 108314053 1 153736810 153736811 A G 20 GENIC homozygous 108314055 1 153737190 153737191 C T 36 GENIC homozygous 108314057 1 153737441 153737442 A G 27 GENIC homozygous 108314059 1 153737513 153737514 A G 40 GENIC homozygous 108314061 1 153737835 153737836 G T 17 GENIC homozygous 108314063 1 153737900 153737901 T C 20 GENIC homozygous 108314065 1 153737993 153737994 C G 23 GENIC homozygous 108314067 1 153738959 153738960 T A 23 GENIC homozygous 108314069 1 153739438 153739439 G A 30 GENIC homozygous 108314071 1 153740013 153740014 T A 32 GENIC homozygous 108314073 1 153740048 153740049 C G 32 GENIC homozygous 108314075 1 153740478 153740479 C T 25 GENIC homozygous 108314077 1 153740675 153740676 A G 26 GENIC homozygous 108314079 1 153741458 153741459 T C 53 GENIC homozygous 108314081