chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 127093103 127093104 A G 8 GENIC homozygous 142766282 X 127095791 127095792 T C 9 GENIC homozygous 140702743 X 127102241 127102242 T A 13 GENIC homozygous 142766283 X 127100163 127100163 T 12 GENIC homozygous 142746625 X 127100586 127100587 A 9 GENIC homozygous 142746626 X 127102333 127102333 TT 10 GENIC homozygous 142746627 X 127103385 127103386 G A 12 GENIC homozygous 142766284 X 127102391 127102391 TTGTTGTT 8 GENIC homozygous 140597184 X 127102371 127102372 T 7 GENIC homozygous 140597183 X 127105777 127105779 AA 7 GENIC homozygous 142746628 X 127106565 127106565 TA 12 GENIC homozygous 142746629 X 127108982 127108983 A G 10 GENIC homozygous 142766286 X 127109880 127109881 A G 14 GENIC homozygous 142766287 X 127110928 127110928 AGTC 13 GENIC homozygous 140597186 X 127112602 127112602 TA 8 GENIC homozygous 142746630 X 127112606 127112607 G T 7 GENIC homozygous 142766288 X 127114447 127114448 A T 10 GENIC homozygous 140702748 X 127115029 127115030 C G 10 GENIC homozygous 140702749 X 127115143 127115144 T C 12 GENIC homozygous 140702750 X 127115696 127115697 A T 16 GENIC homozygous 140702751 X 127116439 127116440 A C 13 GENIC homozygous 140702753 X 127117147 127117148 C T 6 GENIC homozygous 140702755 X 127117604 127117605 C T 13 GENIC homozygous 140702756 X 127117828 127117832 TTTC 7 GENIC homozygous 142746631 X 127121643 127121644 T G 11 GENIC possibly homozygous 140702760 X 127128376 127128378 CT 14 GENIC homozygous 142746632 X 127128479 127128480 G A 11 GENIC homozygous 140702762 X 127132623 127132623 T 8 GENIC homozygous 140597187 X 127138814 127138815 A G 11 GENIC homozygous 140702766 X 127139427 127139428 G A 11 GENIC homozygous 140702767