chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 3099087 3099088 T C 28 GENIC homozygous 530244604 7 3100116 3100117 C CTG 11 GENIC homozygous 694114323 7 3100139 3100140 G GT 10 GENIC homozygous 694114324 7 3100144 3100145 C CG 9 GENIC homozygous 694114325 7 3100150 3100151 C CG 8 GENIC homozygous 694114326 7 3100205 3100206 C CAACA 17 GENIC homozygous 694114327 7 3101946 3101947 G A 26 GENIC homozygous 531004995 7 3102010 3102011 C T 19 GENIC homozygous 531004996 7 3102037 3102038 C T 20 GENIC possibly homozygous 531004997 7 3102052 3102053 G GAA 16 GENIC homozygous 694114328 7 3103097 3103098 A T 28 GENIC homozygous 531004998 7 3104810 3104811 G - 20 GENIC homozygous 694114330 7 3105130 3105131 T C 23 GENIC homozygous 530244605