chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 31647989 31647990 T C 67 GENIC homozygous 116547180 10 31650451 31650452 G T 45 GENIC homozygous 116547182 10 31651684 31651685 T G 38 GENIC homozygous 116547184 10 31651994 31651995 T G 29 GENIC homozygous 116547186 10 31651997 31651998 T G 26 GENIC homozygous 116547188 10 31652538 31652539 T G 15 GENIC homozygous 116547190 10 31653509 31653510 T C 60 GENIC homozygous 116547192 10 31654788 31654789 T A 26 GENIC homozygous 116547194 10 31657153 31657154 T A 42 GENIC homozygous 116547196 10 31658003 31658004 T C 60 GENIC homozygous 117409178 10 31658263 31658264 C G 39 GENIC possibly homozygous 117002194 10 31658774 31658775 A G 44 GENIC homozygous 116547198 10 31658776 31658777 G A 47 GENIC possibly homozygous 116547200 10 31658905 31658906 T C 49 GENIC homozygous 116547202 10 31659038 31659039 T A 29 GENIC homozygous 116547204 10 31659389 31659390 C T 34 GENIC possibly homozygous 116547206 10 31659433 31659434 T G 31 GENIC homozygous 116547208