chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 17968143 17968144 G A 33 GENIC homozygous 805095300 17 17968418 17968419 C T 13 GENIC homozygous 805095301 17 17970531 17970532 T C 12 GENIC homozygous 805095302 17 17973250 17973251 A G 23 GENIC homozygous 805095303 17 17973650 17973651 C T 13 GENIC homozygous 805095304 17 17974779 17974780 T C 14 GENIC homozygous 805095305 17 17974868 17974869 A C 15 GENIC homozygous 805095306 17 17975208 17975209 A T 14 GENIC homozygous 805095307 17 17975962 17975963 C T 27 GENIC homozygous 805095308 17 17976744 17976745 C T 18 GENIC homozygous 805095309 17 17977294 17977295 G A 23 GENIC homozygous 805095310 17 17979545 17979546 G A 19 GENIC homozygous 805095311 17 17980422 17980423 A G 20 GENIC homozygous 805095312 17 17980455 17980456 C T 22 GENIC homozygous 805095313 17 17981521 17981522 C T 13 GENIC homozygous 805095314 17 17982574 17982575 A G 15 GENIC homozygous 805095315 17 17983069 17983070 A G 15 GENIC possibly homozygous 805095316 17 17984201 17984202 A G 17 GENIC homozygous 805095317 17 17984402 17984403 G A 25 GENIC homozygous 805095318 17 17984629 17984630 A T 11 GENIC homozygous 805095319 17 17985000 17985001 G A 24 GENIC homozygous 805095320 17 17985691 17985692 A G 8 GENIC homozygous 805095321 17 17986707 17986708 C T 20 GENIC possibly homozygous 805095322 17 17987759 17987760 G T 22 GENIC homozygous 805095323