chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 155682235 155682236 C 44 GENIC homozygous 128094660 4 155682479 155682479 TT 30 GENIC homozygous 128094661 4 155682881 155682882 T G 53 GENIC homozygous 112896524 4 155686300 155686301 A C 25 GENIC homozygous 112896528 4 155686301 155686302 A G 26 GENIC homozygous 112896530 4 155686396 155686397 T G 31 GENIC possibly homozygous 112896532 4 155686780 155686781 G C 33 GENIC homozygous 112896534 4 155686834 155686834 A 22 GENIC homozygous 128094664 4 155686907 155686907 A 15 GENIC homozygous 128094665 4 155686943 155686943 C 14 GENIC homozygous 128094666 4 155686959 155686960 G A 15 GENIC homozygous 112896536 4 155686967 155686967 A 16 GENIC homozygous 128094667 4 155687362 155687363 T A 45 GENIC homozygous 112896538 4 155687387 155687388 G A 47 GENIC homozygous 112896540 4 155687673 155687674 G A 56 GENIC homozygous 112896542 4 155688889 155688889 T 37 GENIC heterozygous 128094668 4 155688906 155688910 ATTT 31 GENIC homozygous 128094669 4 155689093 155689094 C G 51 GENIC homozygous 112896548 4 155689531 155689532 C T 47 GENIC homozygous 112896550 4 155690460 155690460 A 50 GENIC homozygous 128094670 4 155686830 155686830 T 24 GENIC homozygous 130939443 4 155691113 155691114 T 40 GENIC homozygous 130939444