chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 54606126 54606127 G T 23 GENIC homozygous 142248176 10 54606150 54606151 A G 26 GENIC possibly homozygous 142248177 10 54607018 54607019 T 19 GENIC homozygous 142203479 10 54607023 54607024 T C 19 GENIC homozygous 142248178 10 54607044 54607044 T 14 GENIC heterozygous 146936238 10 54607416 54607416 G 25 GENIC homozygous 142203480 10 54608302 54608318 GTCTGTTCCTCCCAAC 29 GENIC homozygous 142203481 10 54611799 54611800 A G 21 GENIC homozygous 142248179 10 54612246 54612247 G A 28 GENIC homozygous 142248180 10 54612718 54612719 C G 28 GENIC homozygous 142248181 10 54612872 54612873 A 21 GENIC possibly homozygous 142203482 10 54613220 54613220 T 10 GENIC homozygous 142203483 10 54614661 54614661 T 10 GENIC homozygous 142203484 10 54616200 54616201 A G 25 GENIC homozygous 142248182 10 54616367 54616368 A G 23 GENIC homozygous 142248183 10 54616993 54616994 T C 22 GENIC homozygous 142248184 10 54618504 54618505 T C 10 GENIC homozygous 142248185 10 54619077 54619078 G C 20 GENIC homozygous 142248186 10 54619204 54619205 C T 24 GENIC homozygous 142248187 10 54614282 54614283 A G 28 GENIC homozygous 148548439