chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 155682235 155682236 C 47 GENIC homozygous 128094660 4 155682479 155682479 TT 42 GENIC homozygous 128094661 4 155682881 155682882 T G 52 GENIC homozygous 112896524 4 155683727 155683728 G A 52 GENIC possibly homozygous 112896526 4 155686203 155686203 C 29 GENIC heterozygous 128094662 4 155686300 155686301 A C 39 GENIC homozygous 112896528 4 155686301 155686302 A G 39 GENIC homozygous 112896530 4 155686396 155686397 T G 39 GENIC possibly homozygous 112896532 4 155686780 155686781 G C 13 GENIC homozygous 112896534 4 155686827 155686827 C 8 GENIC homozygous 128094663 4 155686834 155686834 A 10 GENIC homozygous 128094664 4 155686907 155686907 A 27 GENIC homozygous 128094665 4 155686943 155686943 C 32 GENIC homozygous 128094666 4 155686959 155686960 G A 34 GENIC homozygous 112896536 4 155686967 155686967 A 32 GENIC possibly homozygous 128094667 4 155687362 155687363 T A 42 GENIC homozygous 112896538 4 155687387 155687388 G A 40 GENIC homozygous 112896540 4 155687673 155687674 G A 41 GENIC homozygous 112896542 4 155688889 155688889 T 43 GENIC heterozygous 128094668 4 155688906 155688910 ATTT 42 GENIC heterozygous 128094669 4 155689066 155689067 G A 40 GENIC homozygous 112896546 4 155689093 155689094 C G 37 GENIC homozygous 112896548 4 155689531 155689532 C T 48 GENIC homozygous 112896550 4 155690256 155690257 A C 41 GENIC homozygous 112896552 4 155690460 155690460 A 42 GENIC homozygous 128094670 4 155686203 155686204 T C 32 GENIC heterozygous 128137163