chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 4474837 4474838 C G 28 GENIC homozygous 113118797 15 4475110 4475111 C T 24 GENIC homozygous 113118799 15 4475786 4475787 C T 20 GENIC homozygous 113118801 15 4476629 4476630 A G 22 GENIC homozygous 112786509 15 4476705 4476706 C T 28 GENIC homozygous 113118803 15 4476747 4476748 C T 29 GENIC homozygous 113118805 15 4476758 4476759 A G 29 GENIC homozygous 112786513 15 4476939 4476941 AG 20 GENIC homozygous 134614629 15 4476942 4476943 G 20 GENIC homozygous 134614630 15 4477257 4477258 T G 23 GENIC homozygous 112786519 15 4477374 4477375 A G 19 GENIC homozygous 112786521 15 4477430 4477431 C T 18 GENIC homozygous 113118808 15 4477590 4477591 G A 19 GENIC homozygous 112786523 15 4477956 4477957 C T 23 GENIC homozygous 113118810 15 4478018 4478019 C T 21 GENIC homozygous 113118812 15 4478043 4478044 G A 28 GENIC homozygous 112786525 15 4478497 4478498 G A 11 GENIC possibly homozygous 134619095 15 4478866 4478867 C T 23 GENIC homozygous 113118814 15 4478550 4478550 GA 10 GENIC homozygous 134242963 15 4479545 4479546 G A 21 GENIC homozygous 112786529 15 4479638 4479639 C G 24 GENIC homozygous 112786531 15 4479661 4479662 C A 21 GENIC homozygous 113118816