chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 139633457 139633458 G A 69 GENIC homozygous 113056186 4 139633534 139633535 C A 50 GENIC homozygous 113056188 4 139634593 139634594 G T 69 GENIC possibly homozygous 112853986 4 139634793 139634794 A C 65 GENIC homozygous 112853988 4 139634845 139634846 A G 63 GENIC homozygous 112853990 4 139635066 139635067 G A 71 GENIC homozygous 113056190 4 139635106 139635107 C T 74 GENIC homozygous 112853992 4 139635679 139635680 G A 62 GENIC homozygous 112853994 4 139635691 139635692 G A 66 GENIC homozygous 113056192 4 139635773 139635774 G A 59 GENIC homozygous 112853996 4 139636407 139636408 A C 49 GENIC homozygous 112854000 4 139636493 139636494 C T 43 GENIC homozygous 113056194 4 139636693 139636694 G A 60 GENIC homozygous 113056196 4 139636961 139636962 T C 54 GENIC homozygous 113056198 4 139637482 139637483 C T 51 GENIC homozygous 112854002 4 139637580 139637581 T G 57 GENIC homozygous 113056200 4 139639468 139639469 G T 52 GENIC possibly homozygous 113056202 4 139633771 139633771 GCTGCC 39 GENIC homozygous 128084367 4 139634990 139634991 T 62 GENIC homozygous 130938103 4 139641222 139641223 C A 51 GENIC homozygous 113056204 4 139641628 139641629 C T 62 GENIC homozygous 113056206 4 139643716 139643717 G A 60 GENIC homozygous 112854042 4 139646425 139646426 G A 49 GENIC homozygous 113056208 4 139646503 139646504 G A 55 GENIC homozygous 113056210 4 139646795 139646796 T C 76 GENIC homozygous 112854052 4 139647780 139647781 C T 66 GENIC homozygous 113056212 4 139650010 139650011 T C 50 GENIC homozygous 112854066 4 139652442 139652443 T C 58 GENIC homozygous 112854076 4 139653576 139653577 C 25 GENIC homozygous 130938104 4 139655707 139655709 AG 56 GENIC homozygous 130938105 4 139656723 139656724 C G 48 GENIC homozygous 113056216 4 139657033 139657033 GAT 52 GENIC homozygous 130938106