chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 101365290 101365291 A G 17 GENIC homozygous 114585113 13 101374823 101374824 G T 18 GENIC homozygous 114585115 13 101376265 101376266 G A 15 GENIC homozygous 114585117 13 101378315 101378316 G A 21 GENIC homozygous 123794498 13 101378744 101378745 A G 23 GENIC homozygous 123794499 13 101378851 101378852 T C 19 GENIC homozygous 114585119 13 101378982 101378983 C T 21 GENIC homozygous 114585121 13 101379266 101379267 G A 21 GENIC homozygous 114585123 13 101379543 101379544 A G 20 GENIC homozygous 114585125 13 101379684 101379685 C T 19 GENIC homozygous 114585127 13 101380029 101380030 A T 22 GENIC homozygous 114585129 13 101380130 101380131 A G 20 GENIC homozygous 114585131 13 101380516 101380517 A C 22 GENIC homozygous 114585133 13 101381025 101381026 A G 16 GENIC homozygous 114585135 13 101381147 101381148 C T 27 GENIC homozygous 114585137 13 101381148 101381149 C T 28 GENIC homozygous 114585139 13 101381232 101381233 T C 25 GENIC homozygous 114585141 13 101381481 101381482 A G 14 GENIC homozygous 114585143 13 101381741 101381742 G C 14 GENIC homozygous 114585145 13 101381881 101381882 A T 25 GENIC homozygous 114585147 13 101381949 101381950 G A 23 GENIC homozygous 114585149 13 101382656 101382657 G A 16 GENIC homozygous 114585151 13 101383019 101383020 G A 18 GENIC homozygous 114585153 13 101383405 101383406 C T 17 GENIC homozygous 114585155 13 101383826 101383827 C T 17 GENIC homozygous 114585157 13 101383897 101383898 T C 13 GENIC homozygous 114585159 13 101384282 101384283 A G 18 GENIC homozygous 114585161 13 101384420 101384421 A G 18 GENIC homozygous 114585163 13 101384633 101384634 G A 18 GENIC homozygous 114585165 13 101385457 101385458 G T 18 GENIC homozygous 114585167 13 101381363 101381376 TGAGGCTTGCTTA 11 GENIC homozygous 131921625