chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 99137057 99137058 C T 16 GENIC homozygous 126111613 13 99137133 99137133 G 12 GENIC homozygous 131136069 13 99137243 99137244 A C 19 GENIC homozygous 114651401 13 99137505 99137506 T C 16 GENIC homozygous 114651403 13 99138359 99138359 C 21 GENIC homozygous 131136070 13 99138744 99138745 C G 13 GENIC homozygous 114651405 13 99139246 99139246 CTG 16 GENIC homozygous 131136071 13 99140337 99140338 T C 21 GENIC homozygous 114651407 13 99140939 99140940 G A 9 GENIC homozygous 126105644 13 99141836 99141837 T G 16 GENIC homozygous 114651409 13 99142019 99142020 G A 21 GENIC homozygous 114651411 13 99142349 99142350 A G 19 GENIC homozygous 114651413 13 99142370 99142371 C T 18 GENIC homozygous 114651415 13 99145597 99145609 TCCCTCCCTCCT 7 GENIC homozygous 131136072 13 99148446 99148447 G A 5 GENIC heterozygous 126105646 13 99148623 99148625 TC 12 GENIC possibly homozygous 131136073 13 99137902 99137902 ATTT 12 GENIC homozygous 132173353 13 99139377 99139378 T G 13 GENIC homozygous 118548022 13 99148537 99148538 T C 5 GENIC heterozygous 118548026 13 99148676 99148677 C G 9 GENIC homozygous 118548027 13 99139410 99139411 C T 10 GENIC homozygous 131140621 13 99145672 99145673 G C 10 GENIC homozygous 114437310 13 99149031 99149031 GTCCTCATGACAGAGCAGGGGGT 9 GENIC homozygous 131136074 13 99149182 99149186 TGTT 14 GENIC homozygous 131136075 13 99149473 99149474 C T 12 GENIC homozygous 131140622 13 99149626 99149627 C T 7 GENIC homozygous 131140623 13 99152061 99152062 G T 8 GENIC homozygous 115155224 13 99152435 99152436 G T 13 GENIC homozygous 114651417 13 99152611 99152612 T C 19 GENIC homozygous 114651419 13 99152906 99152907 C A 14 GENIC homozygous 114651421 13 99153116 99153117 C T 21 GENIC homozygous 114651423 13 99138808 99138809 G T 8 GENIC homozygous 115102276 13 99140687 99140688 G T 14 GENIC homozygous 114791259