chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 2530910 2530910 T 4 GENIC homozygous 130339065 7 2532462 2532463 G T 27 GENIC homozygous 115545354 7 2540639 2540639 G 34 GENIC homozygous 128432187 7 2540654 2540654 G 36 GENIC homozygous 128432188 7 2540710 2540710 C 31 GENIC homozygous 128432189 7 2540748 2540749 C T 35 GENIC homozygous 115976668 7 2540786 2540786 T 32 GENIC homozygous 128432190 7 2540803 2540803 T 26 GENIC heterozygous 128432191 7 2540807 2540808 C T 30 GENIC heterozygous 115976670 7 2540847 2540847 T 32 GENIC homozygous 128432192 7 2540858 2540858 CTGT 34 GENIC homozygous 128432193 7 2547011 2547012 G 31 GENIC homozygous 128432194 7 2547021 2547022 G 31 GENIC homozygous 128432195 7 2547026 2547027 T 34 GENIC homozygous 128432196 7 2547035 2547036 G 34 GENIC homozygous 128432197 7 2547041 2547042 T 35 GENIC homozygous 128432198 7 2543465 2543466 G A 51 GENIC homozygous 134704414 7 2540650 2540651 T G 36 GENIC homozygous 128537812 7 2540651 2540652 G T 36 GENIC homozygous 128537813 7 2540813 2540814 T C 31 GENIC heterozygous 128537814 7 2540747 2540748 A C 35 GENIC homozygous 116268489 7 2540808 2540809 T C 31 GENIC heterozygous 118452554 7 2541023 2541023 T 22 GENIC heterozygous 131430432