chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 40695537 40695538 A G 3 GENIC heterozygous 967715639 12 40696151 40696152 G A 36 GENIC homozygous 967715640 12 40696216 40696217 T C 37 GENIC homozygous 967715641 12 40696648 40696649 A T 19 GENIC homozygous 967715642 12 40696884 40696885 A T 22 GENIC homozygous 967715643 12 40697446 40697447 T C 25 GENIC homozygous 967715644 12 40697467 40697468 C T 28 GENIC homozygous 967715645 12 40698935 40698936 A G 31 GENIC homozygous 967715646 12 40705325 40705326 A G 24 GENIC homozygous 967715647 12 40707476 40707477 C T 42 GENIC homozygous 967715648 12 40709163 40709164 A G 24 GENIC homozygous 967715649