chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 121351511 121351512 A C 24 GENIC homozygous 790188403 7 121351659 121351660 A G 20 GENIC homozygous 790188404 7 121351666 121351667 G A 20 GENIC homozygous 790188405 7 121352112 121352113 A G 26 GENIC homozygous 790188406 7 121352821 121352822 A G 23 GENIC homozygous 790188407 7 121353851 121353852 A T 20 GENIC homozygous 790188408 7 121355445 121355446 T A 18 GENIC possibly homozygous 790188409 7 121357005 121357006 T G 40 GENIC homozygous 790188410 7 121357109 121357110 G A 27 GENIC possibly homozygous 790188411 7 121357662 121357663 C T 31 GENIC homozygous 790188412 7 121361246 121361247 G A 18 GENIC heterozygous 790188413 7 121361280 121361281 C T 10 GENIC possibly homozygous 790188414 7 121364262 121364263 T C 10 GENIC homozygous 790188415 7 121370431 121370432 T C 34 GENIC homozygous 790188416 7 121370670 121370671 G A 20 GENIC homozygous 790188417 7 121372869 121372870 T C 28 GENIC homozygous 790188418 7 121374131 121374132 A G 44 GENIC homozygous 790188419 7 121376034 121376035 G A 39 GENIC homozygous 790188420 7 121376233 121376234 T C 22 GENIC homozygous 790188421 7 121377012 121377013 G A 26 GENIC homozygous 790188422 7 121377413 121377414 A G 26 GENIC homozygous 790188423 7 121378332 121378333 T C 28 GENIC homozygous 790188424 7 121378486 121378487 G A 39 GENIC homozygous 790188425 7 121378756 121378757 T C 28 GENIC homozygous 790188426 7 121380634 121380635 T C 42 GENIC homozygous 790188427 7 121381943 121381944 T C 46 GENIC homozygous 790188428