chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 34617082 34617083 T C 72 GENIC homozygous 506562410 4 34617847 34617848 T C 84 GENIC possibly homozygous 510177606 4 34617899 34617900 T C 85 GENIC possibly homozygous 510177607 4 34618085 34618086 C CAT 55 GENIC homozygous 685520416 4 34618279 34618280 G A 58 GENIC homozygous 510177608 4 34618317 34618318 T C 51 GENIC homozygous 506562411 4 34618717 34618718 T - 69 GENIC homozygous 685520417 4 34619204 34619205 C T 93 GENIC homozygous 510177609 4 34619215 34619216 A - 86 GENIC homozygous 685520418 4 34619379 34619380 T C 70 GENIC homozygous 510177610 4 34619476 34619477 G T 59 GENIC homozygous 506562412 4 34619754 34619755 G A 78 GENIC homozygous 510177611 4 34620301 34620302 A G 56 GENIC homozygous 506562413 4 34620345 34620346 G A 66 GENIC possibly homozygous 510177612 4 34620551 34620552 T - 57 GENIC homozygous 685520419 4 34620737 34620738 C T 52 GENIC homozygous 506562414 4 34621519 34621520 G GA 52 GENIC homozygous 685520420 4 34621528 34621529 T G 58 GENIC possibly homozygous 510177613 4 34622272 34622273 G A 43 GENIC homozygous 510177614 4 34622438 34622439 C T 51 GENIC homozygous 506562415 4 34622716 34622717 A AGTT 31 GENIC homozygous 685520421 4 34622718 34622719 T TTG 36 GENIC homozygous 685520422 4 34622768 34622769 G A 50 GENIC homozygous 506562416 4 34622887 34622888 C T 55 GENIC possibly homozygous 510177615 4 34622915 34622916 T C 47 GENIC homozygous 506562417 4 34623082 34623083 A - 50 GENIC homozygous 685520423 4 34623090 34623091 G A 54 GENIC homozygous 510177616 4 34623287 34623288 G A 48 GENIC possibly homozygous 510177617 4 34623565 34623566 A G 56 GENIC homozygous 506562418 4 34624035 34624036 G A 57 GENIC homozygous 506562419 4 34624232 34624233 T C 65 GENIC homozygous 506562420