chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 11693775 11693776 C T 27 GENIC possibly homozygous 142035403 8 11693968 11693969 C T 13 GENIC homozygous 142035404 8 11694302 11694303 T C 31 GENIC homozygous 142035405 8 11695172 11695176 CACT 16 GENIC homozygous 142017194 8 11696436 11696437 T C 21 GENIC homozygous 142035406 8 11696449 11696450 G A 18 GENIC homozygous 142035407 8 11697243 11697245 CA 18 GENIC homozygous 142017195 8 11698395 11698396 G A 19 GENIC homozygous 142035408 8 11698605 11698606 C T 21 GENIC homozygous 142035409 8 11698965 11698966 A G 22 GENIC homozygous 142035410 8 11699578 11699579 T G 14 GENIC homozygous 142035411 8 11699582 11699583 T C 15 GENIC homozygous 142035412 8 11699711 11699731 CTTGGAACTTCTAGGAGGCA 13 GENIC homozygous 142017196 8 11699764 11699765 G A 18 GENIC homozygous 142035413 8 11700266 11700267 T C 14 GENIC homozygous 142035414 8 11700602 11700602 CACT 20 GENIC homozygous 142017197 8 11701708 11701709 C T 26 GENIC homozygous 142035418 8 11700782 11700783 G C 17 GENIC homozygous 142035415 8 11701031 11701032 G A 33 GENIC homozygous 142035416 8 11701432 11701433 T C 28 GENIC homozygous 142035417 8 11702426 11702427 C T 16 GENIC homozygous 142035419 8 11703082 11703083 T A 29 GENIC homozygous 142035420 8 11703134 11703135 T A 17 GENIC homozygous 142035421 8 11703219 11703220 T C 19 GENIC homozygous 142035422