chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 92579010 92579011 C T 66 GENIC homozygous 142416165 13 92579086 92579086 G 59 GENIC homozygous 142353694 13 92579196 92579197 A C 56 GENIC homozygous 142416166 13 92579458 92579459 T C 62 GENIC homozygous 142416167 13 92579855 92579855 ATTT 34 GENIC homozygous 144926280 13 92580312 92580312 C 49 GENIC homozygous 142353695 13 92580697 92580698 C G 41 GENIC homozygous 142416168 13 92581199 92581199 CTG 58 GENIC homozygous 142353696 13 92581330 92581331 T G 50 GENIC possibly homozygous 142416169 13 92581363 92581364 C T 55 GENIC homozygous 142416170 13 92582290 92582291 T C 44 GENIC homozygous 142416171 13 92582893 92582894 G A 14 GENIC homozygous 142416172 13 92583790 92583791 T G 67 GENIC possibly homozygous 142416173 13 92583973 92583974 G A 46 GENIC homozygous 142416174 13 92584303 92584304 A G 51 GENIC homozygous 142416175 13 92584324 92584325 C T 46 GENIC homozygous 142416176 13 92587551 92587563 TCCCTCCCTCCT 16 GENIC homozygous 142353697 13 92590401 92590402 G A 28 GENIC possibly homozygous 142416177 13 92590492 92590493 T C 12 GENIC possibly homozygous 142416178 13 92590578 92590580 TC 24 GENIC homozygous 142353698 13 92590631 92590632 C G 33 GENIC possibly homozygous 142416179 13 92590986 92590986 GTCCTCATGACAGAGCAGGGGGT 37 GENIC homozygous 142353699 13 92591137 92591141 TGTT 20 GENIC possibly homozygous 142353700 13 92591428 92591429 C T 38 GENIC homozygous 142416180 13 92591581 92591582 C T 30 GENIC homozygous 142416181 13 92593133 92593133 AGGGGGA 8 GENIC homozygous 142353701 13 92594390 92594391 G T 52 GENIC homozygous 142416182 13 92594566 92594567 T C 46 GENIC homozygous 142416183 13 92594861 92594862 C A 41 GENIC homozygous 142416184 13 92595071 92595072 C T 49 GENIC homozygous 142416185 13 92589677 92589678 A T 6 GENIC heterozygous 144934768 13 92587554 92587555 C 16 GENIC homozygous 403346232 13 92587554 92587555 C T 16 GENIC heterozygous 403346231