chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 39302956 39302957 C T 18 GENIC homozygous 139141947 12 39304574 39304575 G A 19 GENIC homozygous 139141950 12 39305069 39305070 C T 8 GENIC homozygous 142340400 12 39305441 39305442 C A 26 GENIC possibly homozygous 139141953 12 39305553 39305554 A G 25 GENIC homozygous 139141954 12 39305583 39305584 T C 26 GENIC possibly homozygous 139141955 12 39305776 39305777 C A 21 GENIC homozygous 142340401 12 39305964 39305965 T C 15 GENIC homozygous 139141956 12 39306623 39306624 T C 24 GENIC homozygous 139141957 12 39307001 39307002 G A 16 GENIC homozygous 139141958