chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 20935744 20935745 T C 57 GENIC possibly homozygous 795646231 14 20936058 20936059 T G 51 GENIC homozygous 795646232 14 20936311 20936312 A G 21 GENIC possibly homozygous 795646233 14 20936543 20936544 G A 44 GENIC possibly homozygous 795646234 14 20937835 20937836 T G 33 GENIC possibly homozygous 795646235 14 20937855 20937856 T A 21 GENIC possibly homozygous 795646236 14 20941643 20941644 A G 16 GENIC homozygous 795646237 14 20941663 20941664 G C 16 GENIC homozygous 795646238 14 20941702 20941703 C A 12 GENIC homozygous 795646239 14 20941705 20941706 G A 12 GENIC homozygous 795646240 14 20942085 20942086 C A 20 GENIC homozygous 795646241 14 20942140 20942141 C G 31 GENIC homozygous 795646242 14 20942232 20942233 C A 28 GENIC homozygous 795646243 14 20946007 20946008 C T 43 GENIC homozygous 795646244 14 20948985 20948986 G C 32 GENIC homozygous 795646245 14 20948989 20948990 T A 31 GENIC homozygous 795646246 14 20948998 20948999 T A 35 GENIC homozygous 795646247 14 20949006 20949007 A T 34 GENIC homozygous 795646248 14 20949008 20949009 G C 31 GENIC homozygous 795646249 14 20951172 20951173 T A 64 GENIC heterozygous 795646250 14 20951648 20951649 A G 42 GENIC homozygous 795646251