chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 97531408 97531409 G A 54 GENIC homozygous 112790102 4 97531936 97531939 AGA 56 GENIC homozygous 128062092 4 97532303 97532304 G T 58 GENIC homozygous 112790106 4 97532406 97532407 T C 72 GENIC homozygous 112790108 4 97533283 97533284 T A 46 GENIC homozygous 112790110 4 97534750 97534751 T C 52 GENIC homozygous 112790116 4 97535066 97535067 A G 55 GENIC homozygous 112790118 4 97536163 97536164 G A 45 GENIC homozygous 112790122 4 97536997 97536998 A G 68 GENIC homozygous 112790124 4 97537716 97537717 G T 52 GENIC homozygous 112790126 4 97538150 97538151 G 47 GENIC homozygous 128062094 4 97538666 97538667 T C 51 GENIC homozygous 112790128 4 97540908 97540909 T C 44 GENIC homozygous 112790134 4 97542181 97542182 T 55 GENIC homozygous 128062095 4 97539350 97539351 T G 40 GENIC possibly homozygous 113534464 4 97540461 97540462 C T 48 GENIC homozygous 113534466 4 97541526 97541527 C T 60 GENIC homozygous 113534468 4 97542469 97542470 A G 56 GENIC homozygous 113534470 4 97543149 97543150 T C 39 GENIC homozygous 113534472 4 97539376 97539379 TTG 35 GENIC homozygous 132058159