chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 82739243 82739244 T G 38 GENIC homozygous 114411855 13 82739791 82739792 A G 36 GENIC homozygous 114411857 13 82741514 82741515 A T 30 GENIC homozygous 114567273 13 82741557 82741558 C T 39 GENIC homozygous 114567274 13 82741837 82741838 A G 34 GENIC homozygous 114411859 13 82741860 82741861 A G 31 GENIC homozygous 114567275 13 82742263 82742264 C T 27 GENIC homozygous 114567276 13 82742328 82742329 C T 33 GENIC homozygous 114567277 13 82742914 82742915 C T 26 GENIC homozygous 114567278 13 82743600 82743601 T C 41 GENIC homozygous 114411861 13 82743607 82743608 T A 39 GENIC homozygous 114411863 13 82746336 82746337 T C 37 GENIC homozygous 114567279 13 82747288 82747289 A G 39 GENIC homozygous 114567280 13 82747814 82747815 A G 33 GENIC homozygous 114411867 13 82748417 82748418 T C 34 GENIC homozygous 114567281 13 82750284 82750285 T A 39 GENIC homozygous 114567282 13 82751114 82751115 A T 36 GENIC homozygous 114567283 13 82751191 82751192 T C 32 GENIC homozygous 114567284 13 82751318 82751319 T G 33 GENIC homozygous 114411875 13 82751341 82751342 A G 31 GENIC homozygous 114411877 13 82752576 82752577 C T 40 GENIC homozygous 114567285 13 82753708 82753709 A C 29 GENIC homozygous 114411887