chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 17239009 17239010 C T 24 GENIC homozygous 117682222 9 17239914 17239915 A G 15 GENIC homozygous 117270258 9 17240034 17240035 T C 15 GENIC homozygous 117270259 9 17241227 17241228 C G 15 GENIC homozygous 117682228 9 17242236 17242237 C T 17 GENIC homozygous 117682230 9 17243579 17243580 T G 20 GENIC homozygous 117682232 9 17244765 17244766 A C 41 GENIC homozygous 117682234 9 17247453 17247454 A C 24 GENIC homozygous 117768340 9 17247910 17247911 T C 16 GENIC homozygous 117682236 9 17252553 17252554 T G 29 GENIC homozygous 117682238 9 17252950 17252951 G T 32 GENIC homozygous 117682240 9 17252965 17252966 T C 38 GENIC homozygous 117682242 9 17253148 17253149 G C 33 GENIC homozygous 117682244 9 17253343 17253344 A G 40 GENIC homozygous 117682246 9 17253351 17253352 A G 37 GENIC homozygous 117682248 9 17253589 17253590 T A 14 GENIC homozygous 117682250 9 17254115 17254116 C T 28 GENIC homozygous 117682252 9 17254180 17254181 G T 31 GENIC homozygous 117682254 9 17254181 17254182 C T 30 GENIC homozygous 117682256