geneid | 9125 |
---|---|
ensemblid | ENSG00000144580.15 |
hgncid | 10445 |
symbol | CNOT9 |
name | CCR4-NOT transcription complex subunit 9 |
refseq_nuc | NM_005444.3 |
refseq_prot | NP_005435.1 |
ensembl_nuc | ENST00000273064.11 |
ensembl_prot | ENSP00000273064.6 |
mane_status | MANE Select |
chr | chr2 |
start | 218568839 |
end | 218597080 |
strand | + |
ver | v1.2 |
region | chr2:218568839-218597080 |
region5000 | chr2:218563839-218602080 |
regionname0 | CNOT9_chr2_218568839_218597080 |
regionname5000 | CNOT9_chr2_218563839_218602080 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 299 | 322 | 88 | 42 | 136 | 12 | 42 | 108 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 900 | 322 | 88 | 42 | 136 | 12 | 42 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2918 | 55 | 7 | 15 | 17 | 5 | 11 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0002 | 0/1 | 2925 | 54 | 3 | 5 | 34 | 2 | 9 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0003 | 0/0 | 2926 | 46 | 4 | 10 | 19 | 2 | 11 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0004 | 0/0 | 2921 | 36 | 3 | 0 | 31 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0005 | 0/0 | 2927 | 14 | 3 | 3 | 5 | 1 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0006 | 0/0 | 2904 | 12 | 12 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0007 | 0/0 | 2919 | 9 | 2 | 2 | 4 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0008 | 0/0 | 2928 | 8 | 0 | 2 | 3 | 1 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0009 | 0/0 | 2921 | 6 | 6 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0010 | 0/0 | 2922 | 6 | 1 | 0 | 5 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0011 | 1/0 | 2921 | 6 | 1 | 2 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0012 | 0/0 | 2925 | 5 | 5 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0013 | 0/0 | 2922 | 5 | 5 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0014 | 0/0 | 2918 | 4 | 4 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0015 | 0/0 | 2923 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0016 | 0/0 | 2924 | 3 | 1 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0017 | 0/0 | 2918 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0018 | 0/0 | 2924 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0019 | 0/0 | 2917 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0020 | 0/0 | 2920 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0021 | 0/0 | 2926 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0022 | 0/0 | 2931 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0023 | 0/0 | 2922 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0024 | 0/0 | 2925 | 2 | 1 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0025 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0026 | 0/0 | 2904 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0027 | 0/0 | 2921 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0028 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0029 | 0/0 | 2927 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0030 | 0/0 | 2919 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0031 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0032 | 0/0 | 2926 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0033 | 0/0 | 2926 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0034 | 0/0 | 2926 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0035 | 0/0 | 2926 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0036 | 0/0 | 2929 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0037 | 0/0 | 2927 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0038 | 0/0 | 2921 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0039 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0040 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0041 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0042 | 0/0 | 2923 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0043 | 0/0 | 2920 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0044 | 0/0 | 2921 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0045 | 0/0 | 2925 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0046 | 0/0 | 2919 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0047 | 0/0 | 2920 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0048 | 0/0 | 2921 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0049 | 0/0 | 2924 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0050 | 0/0 | 2918 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0051 | 0/0 | 2906 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0052 | 0/0 | 2919 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0053 | 0/0 | 2920 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0054 | 0/0 | 2927 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0055 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
t0056 | 0/0 | 2918 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 15 | 0 | 4 | 7 | 1 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0002 | 0/0 | 11 | 0 | 3 | 6 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0003 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0004 | 0/0 | 8 | 0 | 3 | 0 | 2 | 3 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0005 | 0/0 | 6 | 0 | 1 | 4 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 900 | 322 | 88 | 42 | 136 | 12 | 42 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3817 | 55 | 7 | 15 | 17 | 5 | 11 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0002 | 0/1 | 3824 | 54 | 3 | 5 | 34 | 2 | 9 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0003 | 0/0 | 3825 | 46 | 4 | 10 | 19 | 2 | 11 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0004 | 0/0 | 3820 | 36 | 3 | 0 | 31 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0005 | 0/0 | 3826 | 14 | 3 | 3 | 5 | 1 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0006 | 0/0 | 3803 | 12 | 12 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0007 | 0/0 | 3818 | 9 | 2 | 2 | 4 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0008 | 0/0 | 3827 | 8 | 0 | 2 | 3 | 1 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0009 | 0/0 | 3820 | 6 | 6 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0010 | 0/0 | 3821 | 6 | 1 | 0 | 5 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0011 | 1/0 | 3820 | 6 | 1 | 2 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0012 | 0/0 | 3824 | 5 | 5 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0013 | 0/0 | 3821 | 5 | 5 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0014 | 0/0 | 3817 | 4 | 4 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0015 | 0/0 | 3822 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0016 | 0/0 | 3823 | 3 | 1 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0017 | 0/0 | 3817 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0018 | 0/0 | 3823 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0019 | 0/0 | 3816 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0020 | 0/0 | 3819 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0021 | 0/0 | 3825 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0022 | 0/0 | 3830 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0023 | 0/0 | 3821 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0024 | 0/0 | 3824 | 2 | 1 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0025 | 0/0 | 3824 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0026 | 0/0 | 3803 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0027 | 0/0 | 3820 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0028 | 0/0 | 3824 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0029 | 0/0 | 3826 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0030 | 0/0 | 3818 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0031 | 0/0 | 3824 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0032 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0033 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0034 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0035 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0036 | 0/0 | 3828 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0037 | 0/0 | 3826 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0038 | 0/0 | 3820 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0039 | 0/0 | 3827 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0040 | 0/0 | 3831 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0041 | 0/0 | 3831 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0042 | 0/0 | 3822 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0043 | 0/0 | 3819 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0044 | 0/0 | 3820 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0045 | 0/0 | 3824 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0046 | 0/0 | 3818 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0047 | 0/0 | 3819 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0048 | 0/0 | 3820 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0049 | 0/0 | 3823 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0050 | 0/0 | 3817 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0051 | 0/0 | 3805 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0052 | 0/0 | 3818 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0053 | 0/0 | 3819 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0054 | 0/0 | 3826 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0055 | 0/0 | 3824 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
a0001c0001t0056 | 0/0 | 3817 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | copy fasta | chr2 | 218563839 | 218602080 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 11 | 0 | 3 | 6 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 2 | 0 | 2 | 3 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0001 | 0/1 | 7 | 0 | 0 | 5 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0005 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0005g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0005g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0006g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0006g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0007g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0007g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0007g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0008g0001 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0008g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0008g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0009g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0010g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0010g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0010g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0010g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0010g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0010g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0011g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0011g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0011g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0011g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0011g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0012g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0013g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0013g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0013g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0013g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0014g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0014g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0014g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0015g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0015g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0015g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0016g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0016g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0016g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0017g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0018g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0018g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0018g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0019g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0019g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0020g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0020g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0021g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0022g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0022g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0023g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0024g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0024g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0025g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0026g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0027g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0028g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0029g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0030g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0031g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0032g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0033g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0034g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0035g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0036g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0037g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0038g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0039g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0040g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0041g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0042g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0043g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0044g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0045g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0046g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0047g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0048g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0049g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0050g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0051g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0052g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0053g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0054g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0055g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
a0001c0001t0056g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0056 | g0119 | EUR | GBR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0070 | EUR | GBR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00280 | hp2 | a0001 | c0001 | t0008 | g0057 | EUR | FIN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0095 | EUR | FIN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0058 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00673 | hp1 | a0001 | c0001 | t0016 | g0086 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00673 | hp2 | a0001 | c0001 | t0016 | g0064 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01070 | hp2 | a0001 | c0001 | t0011 | g0034 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01081 | hp1 | a0001 | c0001 | t0011 | g0032 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01081 | hp2 | a0001 | c0001 | t0045 | g0096 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01109 | hp1 | a0001 | c0001 | t0042 | g0190 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01256 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01258 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0089 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0046 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01884 | hp2 | a0001 | c0001 | t0040 | g0018 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01975 | hp1 | a0001 | c0001 | t0024 | g0115 | AMR | PEL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | PEL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02015 | hp1 | a0001 | c0001 | t0035 | g0062 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02015 | hp2 | a0001 | c0001 | t0021 | g0011 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02027 | hp1 | a0001 | c0001 | t0008 | g0069 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02055 | hp1 | a0001 | c0001 | t0041 | g0181 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0172 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02071 | hp2 | a0001 | c0001 | t0021 | g0011 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02074 | hp2 | a0001 | c0001 | t0010 | g0203 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0128 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0188 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02145 | hp2 | a0001 | c0001 | t0052 | g0140 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02155 | hp1 | a0001 | c0001 | t0029 | g0082 | EAS | CDX | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | CDX | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | CDX | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02257 | hp1 | a0001 | c0001 | t0009 | g0037 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02257 | hp2 | a0001 | c0001 | t0044 | g0180 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0170 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0174 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02451 | hp1 | a0001 | c0001 | t0011 | g0220 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02451 | hp2 | a0001 | c0001 | t0043 | g0191 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02572 | hp1 | a0001 | c0001 | t0022 | g0018 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02615 | hp2 | a0001 | c0001 | t0014 | g0017 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02622 | hp1 | a0001 | c0001 | t0030 | g0017 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02630 | hp1 | a0001 | c0001 | t0014 | g0167 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02630 | hp2 | a0001 | c0001 | t0053 | g0157 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0171 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0183 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02717 | hp1 | a0001 | c0001 | t0020 | g0177 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02717 | hp2 | a0001 | c0001 | t0012 | g0009 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02723 | hp1 | a0001 | c0001 | t0018 | g0150 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0101 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02818 | hp1 | a0001 | c0001 | t0027 | g0018 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02886 | hp1 | a0001 | c0001 | t0023 | g0035 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02886 | hp2 | a0001 | c0001 | t0012 | g0009 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02896 | hp2 | a0001 | c0001 | t0018 | g0151 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0193 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02897 | hp2 | a0001 | c0001 | t0013 | g0154 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02922 | hp1 | a0001 | c0001 | t0013 | g0155 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02970 | hp1 | a0001 | c0001 | t0017 | g0006 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02970 | hp2 | a0001 | c0001 | t0009 | g0185 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02976 | hp1 | a0001 | c0001 | t0012 | g0009 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02976 | hp2 | a0001 | c0001 | t0046 | g0210 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0038 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03041 | hp1 | a0001 | c0001 | t0012 | g0009 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03041 | hp2 | a0001 | c0001 | t0038 | g0175 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03098 | hp1 | a0001 | c0001 | t0024 | g0153 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03098 | hp2 | a0001 | c0001 | t0012 | g0161 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0173 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03195 | hp1 | a0001 | c0001 | t0054 | g0117 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03195 | hp2 | a0001 | c0001 | t0019 | g0169 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03209 | hp1 | a0001 | c0001 | t0019 | g0168 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03239 | hp2 | a0001 | c0001 | t0036 | g0112 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03453 | hp1 | a0001 | c0001 | t0023 | g0035 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03453 | hp2 | a0001 | c0001 | t0022 | g0189 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03486 | hp1 | a0001 | c0001 | t0018 | g0152 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0159 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0166 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03516 | hp2 | a0001 | c0001 | t0016 | g0165 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03540 | hp1 | a0001 | c0001 | t0013 | g0036 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03579 | hp1 | a0001 | c0001 | t0010 | g0211 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03579 | hp2 | a0001 | c0001 | t0020 | g0017 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0031 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03654 | hp2 | a0001 | c0001 | t0047 | g0204 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0031 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03688 | hp2 | a0001 | c0001 | t0049 | g0212 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0098 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0059 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG04184 | hp1 | a0001 | c0001 | t0008 | g0001 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG04184 | hp2 | a0001 | c0001 | t0007 | g0130 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0087 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG04199 | hp2 | a0001 | c0001 | t0008 | g0001 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG04228 | hp1 | a0001 | c0001 | t0050 | g0143 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | YRI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | YRI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | CHB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | CHB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18951 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18951 | hp2 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18957 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18959 | hp1 | a0001 | c0001 | t0025 | g0109 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18963 | hp1 | a0001 | c0001 | t0011 | g0008 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18964 | hp2 | a0001 | c0001 | t0037 | g0023 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18967 | hp2 | a0001 | c0001 | t0008 | g0106 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18968 | hp2 | a0001 | c0001 | t0033 | g0052 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18971 | hp2 | a0001 | c0001 | t0031 | g0081 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18977 | hp1 | a0001 | c0001 | t0028 | g0085 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18978 | hp1 | a0001 | c0001 | t0051 | g0013 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18981 | hp2 | a0001 | c0001 | t0039 | g0011 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18984 | hp1 | a0001 | c0001 | t0011 | g0008 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19002 | hp2 | a0001 | c0001 | t0034 | g0023 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19011 | hp2 | a0001 | c0001 | t0010 | g0214 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19012 | hp1 | a0001 | c0001 | t0010 | g0209 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19043 | hp1 | a0001 | c0001 | t0009 | g0071 | AFR | LWK | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19056 | hp1 | a0001 | c0001 | t0048 | g0216 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19056 | hp2 | a0001 | c0001 | t0032 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19065 | hp1 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19077 | hp1 | a0001 | c0001 | t0008 | g0065 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19078 | hp2 | a0001 | c0001 | t0007 | g0121 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19079 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19081 | hp2 | a0001 | c0001 | t0010 | g0194 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19087 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19088 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19089 | hp2 | a0001 | c0001 | t0010 | g0207 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19090 | hp2 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19240 | hp1 | a0001 | c0001 | t0015 | g0163 | AFR | YRI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0160 | AFR | YRI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA20129 | hp1 | a0001 | c0001 | t0013 | g0156 | AFR | ASW | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA20129 | hp2 | a0001 | c0001 | t0015 | g0162 | AFR | ASW | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | TSI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0093 | EUR | TSI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0218 | SAS | GIH | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01123 | hp1 | a0001 | c0001 | t0007 | g0133 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02109 | hp1 | a0001 | c0001 | t0009 | g0164 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02109 | hp2 | a0001 | c0001 | t0017 | g0006 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02486 | hp2 | a0001 | c0001 | t0014 | g0178 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02559 | hp1 | a0001 | c0001 | t0026 | g0179 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03471 | hp1 | a0001 | c0001 | t0017 | g0006 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG03471 | hp2 | a0001 | c0001 | t0055 | g0116 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG06807 | hp1 | a0001 | c0001 | t0014 | g0176 | AFR | USA | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
HG06807 | hp2 | a0001 | c0001 | t0015 | g0037 | AFR | USA | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | USA | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA20300 | hp2 | a0001 | c0001 | t0013 | g0036 | AFR | USA | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | LWK | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
NA21309 | hp2 | a0001 | c0001 | t0009 | g0072 | AFR | LWK | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0001 | REF | REF | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0011 | g0158 | REF | REF | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:218568874
|
G | A | 41 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(38): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
5_prime_UTR_variant | MODIFIER | c.-81G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/8 | 81 | chr2 | 218568874 | |||||
chr2:218594723
|
C | A | 1 | a0001c0001t0025 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*447C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 447 | chr2 | 218594723 | |||||
chr2:218594741
|
G | C | 1 | a0001c0001t0050 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*465G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 465 | chr2 | 218594741 | |||||
chr2:218594982
|
A | G | 7 | a0001c0001t0004a0001c0001t0010a0001c0001t0012others(4): Show | 51 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*706A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 706 | chr2 | 218594982 | |||||
chr2:218595214
|
A | G | 1 | a0001c0001t0045 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*938A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 938 | chr2 | 218595214 | |||||
chr2:218595216
|
A | T | 1 | a0001c0001t0013 | 5 | HG02897.hp2 HG02922.hp1 HG03540.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*940A>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 940 | chr2 | 218595216 | |||||
chr2:218595310
|
C | T | 2 | a0001c0001t0043a0001c0001t0044 | 2 | HG02257.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1034C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1034 | chr2 | 218595310 | |||||
chr2:218595330
|
A | C | 1 | a0001c0001t0056 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1054A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1054 | chr2 | 218595330 | |||||
chr2:218595336
|
G | T | 1 | a0001c0001t0042 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1060G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1060 | chr2 | 218595336 | |||||
chr2:218595404
|
C | CTT | 4 | a0001c0001t0015a0001c0001t0019a0001c0001t0054others(1): Show | 7 | HG03195.hp1 HG03195.hp2 HG03209.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1155_*1156dupTT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | ||||
chr2:218595404
|
C | CTTT | 2 | a0001c0001t0014a0001c0001t0016 | 7 | HG00673.hp1 HG00673.hp2 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1154_*1156dupTTT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | ||||
chr2:218595404
|
C | CTTTT | 7 | a0001c0001t0002a0001c0001t0025a0001c0001t0028others(4): Show | 60 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1153_*1156dupTTTT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | ||||
chr2:218595404
|
C | CTTTTT | 7 | a0001c0001t0003a0001c0001t0020a0001c0001t0021others(4): Show | 54 | HG00438.hp2 HG00621.hp2 HG00642.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1152_*1156dupTTTT others(1): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | ||||
chr2:218595404
|
C | CTTTTTT | 4 | a0001c0001t0005a0001c0001t0036a0001c0001t0037others(1): Show | 17 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1151_*1156dupTTTT others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | ||||
chr2:218595404
|
C | CTTTTTTT | 2 | a0001c0001t0008a0001c0001t0039 | 9 | HG00280.hp2 HG01256.hp2 HG01258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1150_*1156dupTTTT others(3): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | ||||
chr2:218595404
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0022 | 2 | HG02572.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1147_*1156dupTTTT others(6): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | ||||
chr2:218595404
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0040a0001c0001t0041 | 2 | HG01884.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1146_*1156dupTTTT others(7): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | ||||
chr2:218595404
|
CT | C | 8 | a0001c0001t0004a0001c0001t0013a0001c0001t0018others(5): Show | 50 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1156delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1156 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | ||||
chr2:218595404
|
CTT | C | 3 | a0001c0001t0007a0001c0001t0046a0001c0001t0052 | 11 | HG00741.hp1 HG01123.hp1 HG02080.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1155_*1156delTT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1155 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | ||||
chr2:218595404
|
CTTT | C | 6 | a0001c0001t0001a0001c0001t0012a0001c0001t0017others(3): Show | 66 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1154_*1156delTTT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1154 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | ||||
chr2:218595404
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0026 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1146_*1156delTTTT others(7): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1146 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | ||||
chr2:218595404
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0006 | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1144_*1156delTTTT others(9): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1144 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | ||||
chr2:218595469
|
GCCGCTAA others(5): Show |
G | 1 | a0001c0001t0051 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1194_*1205delCCGC others(8): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1194 | chr2 | 218595469 | |||||
chr2:218595680
|
C | T | 1 | a0001c0001t0048 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1404C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1404 | chr2 | 218595680 | |||||
chr2:218595701
|
C | T | 1 | a0001c0001t0035 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1425C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1425 | chr2 | 218595701 | |||||
chr2:218595912
|
C | G | 2 | a0001c0001t0017a0001c0001t0052 | 4 | HG02109.hp2 HG02145.hp2 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1636C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1636 | chr2 | 218595912 | |||||
chr2:218596098
|
G | T | 3 | a0001c0001t0021a0001c0001t0031a0001c0001t0039 | 4 | HG02015.hp2 HG02071.hp2 NA18971.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1822G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1822 | chr2 | 218596098 | |||||
chr2:218596201
|
T | A | 2 | a0001c0001t0028a0001c0001t0032 | 2 | NA18977.hp1 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1925T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1925 | chr2 | 218596201 | |||||
chr2:218596357
|
C | T | 3 | a0001c0001t0022a0001c0001t0027a0001c0001t0041 | 4 | HG02055.hp1 HG02572.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2081C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2081 | chr2 | 218596357 | |||||
chr2:218596538
|
A | AAC | 7 | a0001c0001t0013a0001c0001t0023a0001c0001t0029others(4): Show | 12 | HG01109.hp1 HG02155.hp1 HG02886.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2284_*2285dupCA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2286 | INFO_REALIGN_3_PRIME | chr2 | 218596538 | ||||
chr2:218596538
|
A | AACAC | 3 | a0001c0001t0018a0001c0001t0024a0001c0001t0054 | 6 | HG01975.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2282_*2285dupCACA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2286 | INFO_REALIGN_3_PRIME | chr2 | 218596538 | ||||
chr2:218596538
|
A | AACACAC | 1 | a0001c0001t0012 | 5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2280_*2285dupCACA others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2286 | INFO_REALIGN_3_PRIME | chr2 | 218596538 | ||||
chr2:218596538
|
AACAC | A | 1 | a0001c0001t0006 | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2282_*2285delCACA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2282 | INFO_REALIGN_3_PRIME | chr2 | 218596538 | ||||
chr2:218596538
|
AACACAC | A | 6 | a0001c0001t0014a0001c0001t0019a0001c0001t0020others(3): Show | 11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2280_*2285delCACA others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2280 | INFO_REALIGN_3_PRIME | chr2 | 218596538 | ||||
chr2:218596614
|
A | G | 1 | a0001c0001t0026 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2338A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2338 | chr2 | 218596614 | |||||
chr2:218596736
|
C | G | 2 | a0001c0001t0034a0001c0001t0037 | 2 | NA18964.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2460C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2460 | chr2 | 218596736 | |||||
chr2:218596805
|
T | G | 1 | a0001c0001t0033 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2529T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2529 | chr2 | 218596805 | |||||
chr2:218597036
|
A | AG | 5 | a0001c0001t0004a0001c0001t0010a0001c0001t0012others(2): Show | 49 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2765dupG | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2766 | INFO_REALIGN_3_PRIME | chr2 | 218597036 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:218569065
|
C | G | 1 | a0001c0001t0011g0220 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.24+87C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569065 | ||||||
chr2:218569073
|
T | G | 1 | a0001c0001t0003g0043 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.24+95T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569073 | ||||||
chr2:218569165
|
C | A | 102 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(99): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.24+187C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569165 | ||||||
chr2:218569322
|
A | G | 34 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(31): Show | 46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+344A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569322 | ||||||
chr2:218569341
|
C | T | 1 | a0001c0001t0003g0113 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.24+363C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569341 | ||||||
chr2:218569413
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.24+435T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569413 | ||||||
chr2:218569471
|
A | G | 180 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(177): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.24+493A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569471 | ||||||
chr2:218569485
|
C | T | 144 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(141): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.24+507C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569485 | ||||||
chr2:218569537
|
T | C | 3 | a0001c0001t0024g0115a0001c0001t0054g0117a0001c0001t0055g0116 | 3 | HG01975.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.24+559T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569537 | ||||||
chr2:218569889
|
T | C | 3 | a0001c0001t0024g0115a0001c0001t0054g0117a0001c0001t0055g0116 | 3 | HG01975.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.24+911T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569889 | ||||||
chr2:218570094
|
A | G | 3 | a0001c0001t0024g0115a0001c0001t0054g0117a0001c0001t0055g0116 | 3 | HG01975.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.24+1116A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218570094 | ||||||
chr2:218570262
|
T | C | 4 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(1): Show | 4 | HG00642.hp2 HG00741.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+1284T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218570262 | ||||||
chr2:218570565
|
G | A | 102 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(99): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.24+1587G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218570565 | ||||||
chr2:218570730
|
C | T | 1 | a0001c0001t0036g0112 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.24+1752C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218570730 | ||||||
chr2:218571119
|
C | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(239): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.24+2141C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571119 | ||||||
chr2:218571203
|
T | G | 1 | a0001c0001t0003g0048 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.24+2225T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571203 | ||||||
chr2:218571278
|
C | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(241): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.24+2300C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571278 | ||||||
chr2:218571574
|
C | CT | 95 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(92): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.24+2610dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218571574 | |||||
chr2:218571574
|
C | CTT | 7 | a0001c0001t0002g0030a0001c0001t0002g0107a0001c0001t0002g0111others(4): Show | 9 | HG01261.hp2 HG03490.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.24+2609_24+2610dup others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218571574 | |||||
chr2:218571574
|
CT | C | 4 | a0001c0001t0010g0194a0001c0001t0012g0009a0001c0001t0012g0161others(1): Show | 7 | HG01975.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+2610delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218571574 | |||||
chr2:218571586
|
T | C | 6 | a0001c0001t0009g0037a0001c0001t0009g0164a0001c0001t0015g0037others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.24+2608T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571586 | ||||||
chr2:218571729
|
G | A | 34 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(31): Show | 46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+2751G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571729 | ||||||
chr2:218571738
|
A | AT | 102 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(99): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.24+2778dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218571738 | |||||
chr2:218571738
|
A | ATT | 51 | a0001c0001t0002g0029a0001c0001t0002g0097a0001c0001t0002g0103others(48): Show | 57 | HG00741.hp2 HG01081.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.24+2777_24+2778dup others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218571738 | |||||
chr2:218571738
|
AT | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(47): Show | 74 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.24+2778delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218571738 | |||||
chr2:218571739
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.24+2761T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571739 | ||||||
chr2:218571816
|
C | T | 2 | a0001c0001t0003g0192a0001c0001t0005g0193 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.24+2838C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571816 | ||||||
chr2:218572159
|
A | G | 1 | a0001c0001t0002g0095 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.24+3181A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572159 | ||||||
chr2:218572194
|
G | A | 8 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0166others(5): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.24+3216G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572194 | ||||||
chr2:218572227
|
G | A | 11 | a0001c0001t0014g0017a0001c0001t0014g0167a0001c0001t0014g0176others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.24+3249G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572227 | ||||||
chr2:218572249
|
A | T | 136 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(133): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.24+3271A>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572249 | ||||||
chr2:218572295
|
T | C | 8 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0166others(5): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.24+3317T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572295 | ||||||
chr2:218572520
|
A | G | 1 | a0001c0001t0004g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.24+3542A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572520 | ||||||
chr2:218572592
|
C | T | 12 | a0001c0001t0013g0036a0001c0001t0013g0154a0001c0001t0013g0155others(9): Show | 14 | HG01975.hp1 HG02723.hp1 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.24+3614C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572592 | ||||||
chr2:218572753
|
T | C | 102 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(99): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.24+3775T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572753 | ||||||
chr2:218572873
|
G | C | 180 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(177): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.24+3895G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572873 | ||||||
chr2:218572945
|
G | C | 2 | a0001c0001t0006g0015a0001c0001t0006g0166 | 4 | HG02723.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+3967G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572945 | ||||||
chr2:218573115
|
C | T | 1 | a0001c0001t0012g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.24+4137C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573115 | ||||||
chr2:218573223
|
C | T | 2 | a0001c0001t0012g0009a0001c0001t0012g0161 | 5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+4245C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573223 | ||||||
chr2:218573224
|
A | C | 144 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(141): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.24+4246A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573224 | ||||||
chr2:218573258
|
T | C | 1 | a0001c0001t0023g0035 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.24+4280T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573258 | ||||||
chr2:218573297
|
A | G | 12 | a0001c0001t0013g0036a0001c0001t0013g0154a0001c0001t0013g0155others(9): Show | 14 | HG01975.hp1 HG02723.hp1 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.24+4319A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573297 | ||||||
chr2:218573318
|
TA | T | 172 | a0001c0001t0001g0034a0001c0001t0001g0145a0001c0001t0001g0146others(169): Show | 218 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.24+4360delA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218573318 | |||||
chr2:218573318
|
TAAAAAAA others(1): Show |
T | 8 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0166others(5): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.24+4353_24+4360del others(8): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218573318 | |||||
chr2:218573438
|
A | G | 2 | a0001c0001t0012g0009a0001c0001t0012g0161 | 5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+4460A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573438 | ||||||
chr2:218573445
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.24+4467G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573445 | ||||||
chr2:218573543
|
A | G | 1 | a0001c0001t0002g0028 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.24+4565A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573543 | ||||||
chr2:218573627
|
TTTTC | T | 4 | a0001c0001t0002g0021a0001c0001t0002g0056a0001c0001t0003g0021others(1): Show | 4 | HG00280.hp2 HG01255.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+4653_24+4656del others(4): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218573627 | |||||
chr2:218573636
|
C | T | 144 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(141): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.24+4658C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573636 | ||||||
chr2:218573722
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.24+4744A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573722 | ||||||
chr2:218573767
|
A | G | 1 | a0001c0001t0004g0218 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.24+4789A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573767 | ||||||
chr2:218573826
|
G | A | 1 | a0001c0001t0041g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.24+4848G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573826 | ||||||
chr2:218573939
|
A | G | 1 | a0001c0001t0006g0166 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.24+4961A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573939 | ||||||
chr2:218573940
|
A | G | 11 | a0001c0001t0014g0017a0001c0001t0014g0167a0001c0001t0014g0176others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.24+4962A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573940 | ||||||
chr2:218574073
|
G | A | 1 | a0001c0001t0056g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.24+5095G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574073 | ||||||
chr2:218574081
|
C | T | 1 | a0001c0001t0003g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.24+5103C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574081 | ||||||
chr2:218574094
|
T | C | 245 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(242): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.24+5116T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574094 | ||||||
chr2:218574116
|
A | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(239): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.24+5138A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574116 | ||||||
chr2:218574592
|
G | A | 5 | a0001c0001t0006g0016a0001c0001t0006g0170a0001c0001t0006g0171others(2): Show | 7 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+5614G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574592 | ||||||
chr2:218574630
|
A | G | 2 | a0001c0001t0012g0009a0001c0001t0012g0161 | 5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+5652A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574630 | ||||||
chr2:218574814
|
T | G | 1 | a0001c0001t0014g0167 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.25-5747T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574814 | ||||||
chr2:218574915
|
G | A | 1 | a0001c0001t0006g0166 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.25-5646G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574915 | ||||||
chr2:218574973
|
C | A | 2 | a0001c0001t0015g0162a0001c0001t0015g0163 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.25-5588C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574973 | ||||||
chr2:218575123
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.25-5438A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575123 | ||||||
chr2:218575387
|
C | CT | 40 | a0001c0001t0001g0144a0001c0001t0004g0010a0001c0001t0004g0019others(37): Show | 55 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(52): Show |
intron_variant | MODIFIER | c.25-5157dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218575387 | |||||
chr2:218575424
|
A | AGCTCAGG others(33): Show |
2 | a0001c0001t0002g0095a0001c0001t0005g0058 | 2 | HG00323.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.25-5135_25-5096dup others(40): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218575424 | |||||
chr2:218575446
|
C | T | 15 | a0001c0001t0003g0182a0001c0001t0003g0184a0001c0001t0003g0187others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.25-5115C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575446 | ||||||
chr2:218575513
|
C | T | 8 | a0001c0001t0009g0037a0001c0001t0009g0164a0001c0001t0015g0037others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.25-5048C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575513 | ||||||
chr2:218575568
|
A | G | 2 | a0001c0001t0006g0015a0001c0001t0006g0166 | 4 | HG02723.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-4993A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575568 | ||||||
chr2:218575627
|
A | G | 8 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0166others(5): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.25-4934A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575627 | ||||||
chr2:218575697
|
C | T | 3 | a0001c0001t0004g0215a0001c0001t0004g0217a0001c0001t0048g0216 | 3 | NA19009.hp2 NA19056.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.25-4864C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575697 | ||||||
chr2:218575705
|
A | G | 34 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(31): Show | 46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-4856A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575705 | ||||||
chr2:218575727
|
G | A | 9 | a0001c0001t0003g0182a0001c0001t0003g0184a0001c0001t0003g0187others(6): Show | 9 | HG02145.hp1 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.25-4834G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575727 | ||||||
chr2:218575810
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(239): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.25-4751A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575810 | ||||||
chr2:218575843
|
G | A | 5 | a0001c0001t0022g0018a0001c0001t0022g0189a0001c0001t0027g0018others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-4718G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575843 | ||||||
chr2:218575868
|
T | C | 2 | a0001c0001t0001g0120a0001c0001t0007g0121 | 2 | NA18977.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.25-4693T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575868 | ||||||
chr2:218575920
|
A | C | 13 | a0001c0001t0004g0010a0001c0001t0004g0040a0001c0001t0004g0041others(10): Show | 19 | HG02135.hp2 HG02165.hp2 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.25-4641A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575920 | ||||||
chr2:218576184
|
G | T | 11 | a0001c0001t0014g0017a0001c0001t0014g0167a0001c0001t0014g0176others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.25-4377G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576184 | ||||||
chr2:218576442
|
G | A | 1 | a0001c0001t0003g0059 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.25-4119G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576442 | ||||||
chr2:218576457
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.25-4104G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576457 | ||||||
chr2:218576704
|
A | G | 1 | a0001c0001t0050g0143 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.25-3857A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576704 | ||||||
chr2:218576705
|
T | C | 180 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(177): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.25-3856T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576705 | ||||||
chr2:218576880
|
C | T | 180 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(177): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.25-3681C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576880 | ||||||
chr2:218576966
|
C | CA | 164 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(161): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.25-3580dupA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218576966 | |||||
chr2:218576970
|
A | AC | 2 | a0001c0001t0012g0009a0001c0001t0012g0161 | 5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-3591_25-3590ins others(1): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576970 | ||||||
chr2:218577694
|
A | G | 1 | a0001c0001t0002g0088 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.25-2867A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218577694 | ||||||
chr2:218577702
|
C | T | 36 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(33): Show | 51 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(48): Show |
intron_variant | MODIFIER | c.25-2859C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218577702 | ||||||
chr2:218577776
|
A | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(47): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.25-2785A>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218577776 | ||||||
chr2:218577795
|
A | C | 1 | a0001c0001t0009g0164 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.25-2766A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218577795 | ||||||
chr2:218577917
|
G | A | 1 | a0001c0001t0038g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.25-2644G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218577917 | ||||||
chr2:218578056
|
G | C | 2 | a0001c0001t0007g0159a0001c0001t0007g0160 | 2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.25-2505G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218578056 | ||||||
chr2:218578278
|
A | C | 180 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(177): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.25-2283A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218578278 | ||||||
chr2:218578359
|
C | A | 2 | a0001c0001t0003g0192a0001c0001t0005g0193 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.25-2202C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218578359 | ||||||
chr2:218578406
|
A | G | 19 | a0001c0001t0009g0037a0001c0001t0009g0164a0001c0001t0014g0017others(16): Show | 19 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.25-2155A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218578406 | ||||||
chr2:218578514
|
A | G | 1 | a0001c0001t0007g0142 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.25-2047A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218578514 | ||||||
chr2:218578994
|
A | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(46): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.25-1567A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218578994 | ||||||
chr2:218579179
|
A | G | 1 | a0001c0001t0010g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.25-1382A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579179 | ||||||
chr2:218579337
|
A | G | 1 | a0001c0001t0049g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.25-1224A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579337 | ||||||
chr2:218579388
|
T | C | 2 | a0001c0001t0043g0191a0001c0001t0044g0180 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.25-1173T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579388 | ||||||
chr2:218579392
|
G | A | 11 | a0001c0001t0014g0017a0001c0001t0014g0167a0001c0001t0014g0176others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.25-1169G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579392 | ||||||
chr2:218579455
|
A | T | 34 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(31): Show | 46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-1106A>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579455 | ||||||
chr2:218579509
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.25-1052C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579509 | ||||||
chr2:218579520
|
A | G | 1 | a0001c0001t0024g0153 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.25-1041A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579520 | ||||||
chr2:218579609
|
C | G | 36 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(33): Show | 51 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(48): Show |
intron_variant | MODIFIER | c.25-952C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579609 | ||||||
chr2:218579631
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.25-930C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579631 | ||||||
chr2:218579663
|
T | G | 2 | a0001c0001t0002g0061a0001c0001t0002g0107 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.25-898T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579663 | ||||||
chr2:218579818
|
A | G | 3 | a0001c0001t0014g0178a0001c0001t0016g0086a0001c0001t0042g0190 | 3 | HG00673.hp1 HG01109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.25-743A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579818 | ||||||
chr2:218579871
|
T | G | 34 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(31): Show | 46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-690T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579871 | ||||||
chr2:218579922
|
G | A | 1 | a0001c0001t0035g0062 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.25-639G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579922 | ||||||
chr2:218579982
|
C | CT | 46 | a0001c0001t0001g0141a0001c0001t0002g0012a0001c0001t0002g0054others(43): Show | 58 | HG00558.hp2 HG00621.hp1 HG01175.hp1 others(55): Show |
intron_variant | MODIFIER | c.25-562dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218579982 | |||||
chr2:218580158
|
G | A | 1 | a0001c0001t0042g0190 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.25-403G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218580158 | ||||||
chr2:218580333
|
A | G | 2 | a0001c0001t0007g0159a0001c0001t0007g0160 | 2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.25-228A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218580333 | ||||||
chr2:218580402
|
T | G | 1 | a0001c0001t0049g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.25-159T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218580402 | ||||||
chr2:218580442
|
T | C | 144 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(141): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.25-119T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218580442 | ||||||
chr2:218581099
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.204+359G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581099 | ||||||
chr2:218581129
|
A | G | 5 | a0001c0001t0009g0037a0001c0001t0015g0037a0001c0001t0015g0162others(2): Show | 5 | HG02257.hp1 HG03516.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+389A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581129 | ||||||
chr2:218581137
|
GAA | G | 144 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(141): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.204+399_204+400del others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 218581137 | |||||
chr2:218581159
|
T | G | 1 | a0001c0001t0002g0092 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.204+419T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581159 | ||||||
chr2:218581170
|
C | CT | 8 | a0001c0001t0002g0088a0001c0001t0006g0015a0001c0001t0006g0016others(5): Show | 12 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.204+446dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 218581170 | |||||
chr2:218581170
|
CT | C | 35 | a0001c0001t0003g0192a0001c0001t0004g0010a0001c0001t0004g0019others(32): Show | 50 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(47): Show |
intron_variant | MODIFIER | c.204+446delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 218581170 | |||||
chr2:218581171
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.204+431T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581171 | ||||||
chr2:218581175
|
T | C | 1 | a0001c0001t0004g0196 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.204+435T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581175 | ||||||
chr2:218581191
|
C | T | 1 | a0001c0001t0006g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.204+451C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581191 | ||||||
chr2:218581192
|
G | A | 11 | a0001c0001t0014g0017a0001c0001t0014g0167a0001c0001t0014g0176others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+452G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581192 | ||||||
chr2:218581267
|
G | C | 245 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(242): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.204+527G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581267 | ||||||
chr2:218581402
|
C | T | 1 | a0001c0001t0049g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.204+662C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581402 | ||||||
chr2:218581418
|
C | T | 1 | a0001c0001t0002g0084 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.204+678C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581418 | ||||||
chr2:218581734
|
C | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0103a0001c0001t0003g0012others(1): Show | 4 | HG02083.hp2 NA18995.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+994C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581734 | ||||||
chr2:218581754
|
G | A | 144 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(141): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.204+1014G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581754 | ||||||
chr2:218581778
|
A | G | 11 | a0001c0001t0014g0017a0001c0001t0014g0167a0001c0001t0014g0176others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+1038A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581778 | ||||||
chr2:218581987
|
T | C | 8 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0166others(5): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.205-984T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581987 | ||||||
chr2:218582090
|
GA | G | 102 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(99): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.205-873delA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 218582090 | |||||
chr2:218582105
|
T | C | 1 | a0001c0001t0045g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.205-866T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582105 | ||||||
chr2:218582242
|
C | T | 2 | a0001c0001t0005g0188a0001c0001t0010g0211 | 2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.205-729C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582242 | ||||||
chr2:218582400
|
A | G | 8 | a0001c0001t0009g0037a0001c0001t0009g0164a0001c0001t0015g0037others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-571A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582400 | ||||||
chr2:218582456
|
C | T | 3 | a0001c0001t0003g0187a0001c0001t0005g0186a0001c0001t0009g0185 | 3 | HG02280.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.205-515C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582456 | ||||||
chr2:218582487
|
G | C | 1 | a0001c0001t0002g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-484G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582487 | ||||||
chr2:218582488
|
A | T | 1 | a0001c0001t0002g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-483A>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582488 | ||||||
chr2:218582490
|
A | G | 1 | a0001c0001t0002g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-481A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582490 | ||||||
chr2:218582492
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-479C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582492 | ||||||
chr2:218582494
|
T | A | 1 | a0001c0001t0002g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-477T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582494 | ||||||
chr2:218582496
|
C | A | 1 | a0001c0001t0002g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-475C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582496 | ||||||
chr2:218582498
|
G | T | 1 | a0001c0001t0002g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-473G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582498 | ||||||
chr2:218582590
|
T | G | 1 | a0001c0001t0050g0143 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.205-381T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582590 | ||||||
chr2:218582665
|
G | A | 36 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(33): Show | 51 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(48): Show |
intron_variant | MODIFIER | c.205-306G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582665 | ||||||
chr2:218582685
|
G | A | 34 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(31): Show | 46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.205-286G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582685 | ||||||
chr2:218582689
|
C | CA | 37 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(34): Show | 52 | HG00558.hp2 HG00621.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.205-271dupA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 218582689 | |||||
chr2:218582889
|
CT | C | 54 | a0001c0001t0001g0122a0001c0001t0001g0146a0001c0001t0003g0066others(51): Show | 62 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(59): Show |
intron_variant | MODIFIER | c.205-69delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 218582889 | |||||
chr2:218583189
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(241): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.320+103A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583189 | ||||||
chr2:218583219
|
G | C | 1 | a0001c0001t0004g0199 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.320+133G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583219 | ||||||
chr2:218583219
|
GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0004g0213 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.320+135_320+158del others(24): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583219 | |||||
chr2:218583219
|
GTGTGTGT others(27): Show |
G | 1 | a0001c0001t0010g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.320+135_320+168del others(34): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583219 | |||||
chr2:218583221
|
GTGTGTGT others(13): Show |
G | 1 | a0001c0001t0004g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.320+137_320+156del others(20): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583221 | |||||
chr2:218583221
|
GTGTGTGT others(15): Show |
G | 6 | a0001c0001t0004g0041a0001c0001t0004g0195a0001c0001t0004g0198others(3): Show | 7 | HG02074.hp2 HG03654.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.320+137_320+158del others(22): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583221 | |||||
chr2:218583221
|
GTGTGTGT others(17): Show |
G | 13 | a0001c0001t0004g0010a0001c0001t0004g0038a0001c0001t0004g0040others(10): Show | 18 | HG00558.hp2 HG00621.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.320+137_320+160del others(24): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583221 | |||||
chr2:218583221
|
GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0004g0200 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.320+137_320+164del others(28): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583221 | |||||
chr2:218583223
|
GTGTGTGT others(11): Show |
G | 4 | a0001c0001t0004g0208a0001c0001t0010g0194a0001c0001t0010g0207others(1): Show | 4 | NA18968.hp1 NA19012.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.320+139_320+156del others(18): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583223 | |||||
chr2:218583223
|
GTGTGTGT others(13): Show |
G | 4 | a0001c0001t0004g0019a0001c0001t0004g0039a0001c0001t0004g0199others(1): Show | 7 | HG02083.hp1 NA18939.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.320+139_320+158del others(20): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583223 | |||||
chr2:218583223
|
GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0004g0042 | 2 | NA18612.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.320+139_320+160del others(22): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583223 | |||||
chr2:218583225
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0005g0188 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.320+141_320+152del others(12): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | |||||
chr2:218583225
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0001g0147 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.320+141_320+154del others(14): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | |||||
chr2:218583225
|
GTGTGTGT others(9): Show |
G | 2 | a0001c0001t0003g0187a0001c0001t0009g0183 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.320+141_320+156del others(16): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | |||||
chr2:218583225
|
GTGTGTGT others(11): Show |
G | 3 | a0001c0001t0003g0184a0001c0001t0005g0186a0001c0001t0009g0185 | 3 | HG02280.hp2 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.320+141_320+158del others(18): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | |||||
chr2:218583225
|
GTGTGTGT others(13): Show |
G | 1 | a0001c0001t0003g0182 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.320+141_320+160del others(20): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | |||||
chr2:218583225
|
GTGTGTGT others(21): Show |
G | 4 | a0001c0001t0002g0022a0001c0001t0003g0093a0001c0001t0005g0108others(1): Show | 5 | HG00733.hp2 HG00735.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.320+141_320+168del others(28): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | |||||
chr2:218583225
|
GTGTGTGT others(23): Show |
G | 1 | a0001c0001t0012g0009 | 4 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.320+141_320+170del others(30): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | |||||
chr2:218583227
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0001g0125 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.320+143_320+156del others(14): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | |||||
chr2:218583227
|
GTGTGTGT others(9): Show |
G | 2 | a0001c0001t0001g0032a0001c0001t0011g0032 | 2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.320+143_320+158del others(16): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | |||||
chr2:218583227
|
GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0041g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.320+143_320+160del others(18): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | |||||
chr2:218583227
|
GTGTGTGT others(13): Show |
G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.320+143_320+162del others(20): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | |||||
chr2:218583227
|
GTGTGTGT others(15): Show |
G | 6 | a0001c0001t0003g0192a0001c0001t0005g0193a0001c0001t0012g0161others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.320+143_320+164del others(22): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | |||||
chr2:218583227
|
GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0003g0076 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.320+143_320+166del others(24): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | |||||
chr2:218583227
|
GTGTGTGT others(19): Show |
G | 5 | a0001c0001t0002g0050a0001c0001t0002g0055a0001c0001t0002g0063others(2): Show | 5 | HG00639.hp2 HG02155.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+143_320+168del others(26): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | |||||
chr2:218583227
|
GTGTGTGT others(21): Show |
G | 63 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0007others(60): Show | 86 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.320+143_320+170del others(28): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | |||||
chr2:218583227
|
GTGTGTGT others(25): Show |
G | 1 | a0001c0001t0002g0067 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.320+143_320+174del others(32): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | |||||
chr2:218583229
|
GTGTGTCT others(3): Show |
G | 5 | a0001c0001t0001g0008a0001c0001t0001g0120a0001c0001t0001g0122others(2): Show | 7 | NA18950.hp2 NA18953.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.320+145_320+154del others(10): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | |||||
chr2:218583229
|
GTGTGTCT others(5): Show |
G | 8 | a0001c0001t0001g0013a0001c0001t0001g0118a0001c0001t0001g0131others(5): Show | 9 | HG00280.hp1 HG00639.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.320+145_320+156del others(12): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | |||||
chr2:218583229
|
GTGTGTCT others(7): Show |
G | 6 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0141others(3): Show | 16 | HG00558.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.320+145_320+158del others(14): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | |||||
chr2:218583229
|
GTGTGTCT others(9): Show |
G | 6 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0145others(3): Show | 12 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.320+145_320+160del others(16): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | |||||
chr2:218583229
|
GTGTGTCT others(11): Show |
G | 2 | a0001c0001t0001g0127a0001c0001t0042g0190 | 2 | HG01109.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.320+145_320+162del others(18): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | |||||
chr2:218583229
|
GTGTGTCT others(13): Show |
G | 2 | a0001c0001t0050g0143a0001c0001t0056g0119 | 2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.320+145_320+164del others(20): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | |||||
chr2:218583229
|
GTGTGTCT others(15): Show |
G | 1 | a0001c0001t0001g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.320+145_320+166del others(22): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | |||||
chr2:218583229
|
GTGTGTCT others(19): Show |
G | 40 | a0001c0001t0002g0005a0001c0001t0002g0053a0001c0001t0002g0061others(37): Show | 46 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.320+145_320+170del others(26): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | |||||
chr2:218583229
|
GTGTGTCT others(21): Show |
G | 1 | a0001c0001t0009g0164 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.320+145_320+172del others(28): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | |||||
chr2:218583231
|
GTGTCTCT others(3): Show |
G | 1 | a0001c0001t0007g0159 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.320+147_320+156del others(10): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583231 | |||||
chr2:218583231
|
GTGTCTCT others(5): Show |
G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA19076.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.320+147_320+158del others(12): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583231 | |||||
chr2:218583231
|
GTGTCTCT others(11): Show |
G | 2 | a0001c0001t0001g0134a0001c0001t0022g0189 | 2 | HG03453.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.320+147_320+164del others(18): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583231 | |||||
chr2:218583231
|
GTGTCTCT others(17): Show |
G | 4 | a0001c0001t0002g0026a0001c0001t0003g0026a0001c0001t0003g0027others(1): Show | 5 | HG02155.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+147_320+170del others(24): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583231 | |||||
chr2:218583231
|
GTGTCTCT others(27): Show |
G | 8 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0166others(5): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.320+147_320+180del others(34): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583231 | |||||
chr2:218583233
|
GTC | G | 2 | a0001c0001t0001g0033a0001c0001t0052g0140 | 3 | HG02145.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.320+200_320+201del others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | |||||
chr2:218583233
|
GTCTC | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0148a0001c0001t0017g0006 | 6 | HG02109.hp2 HG02486.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.320+198_320+201del others(4): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | |||||
chr2:218583233
|
GTCTCTCT others(1): Show |
G | 3 | a0001c0001t0001g0139a0001c0001t0013g0155a0001c0001t0053g0157 | 3 | HG02572.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.320+194_320+201del others(8): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | |||||
chr2:218583233
|
GTCTCTCT others(3): Show |
G | 3 | a0001c0001t0004g0020a0001c0001t0013g0156a0001c0001t0024g0115 | 5 | HG01975.hp1 HG02559.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+192_320+201del others(10): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | |||||
chr2:218583233
|
GTCTCTCT others(5): Show |
G | 4 | a0001c0001t0013g0036a0001c0001t0013g0154a0001c0001t0023g0035others(1): Show | 6 | HG02886.hp1 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.320+190_320+201del others(12): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | |||||
chr2:218583233
|
GTCTCTCT others(7): Show |
G | 3 | a0001c0001t0018g0151a0001c0001t0024g0153a0001c0001t0055g0116 | 3 | HG02896.hp2 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.320+188_320+201del others(14): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | |||||
chr2:218583233
|
GTCTCTCT others(11): Show |
G | 1 | a0001c0001t0018g0150 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.320+184_320+201del others(18): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | |||||
chr2:218583233
|
GTCTCTCT others(13): Show |
G | 1 | a0001c0001t0001g0137 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.320+182_320+201del others(20): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | |||||
chr2:218583233
|
GTCTCTCT others(15): Show |
G | 2 | a0001c0001t0002g0083a0001c0001t0016g0165 | 2 | HG03516.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.320+180_320+201del others(22): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | |||||
chr2:218583235
|
C | G | 1 | a0001c0001t0018g0152 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.320+149C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583235 | ||||||
chr2:218583237
|
C | G | 3 | a0001c0001t0001g0033a0001c0001t0018g0152a0001c0001t0052g0140 | 4 | HG02145.hp2 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.320+151C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583237 | ||||||
chr2:218583239
|
C | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0148others(3): Show | 10 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.320+153C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583239 | ||||||
chr2:218583241
|
C | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0148others(5): Show | 12 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.320+155C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583241 | ||||||
chr2:218583243
|
C | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0139others(8): Show | 15 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.320+157C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583243 | ||||||
chr2:218583245
|
C | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0139others(8): Show | 15 | HG01975.hp1 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.320+159C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583245 | ||||||
chr2:218583247
|
C | G | 10 | a0001c0001t0001g0139a0001c0001t0011g0220a0001c0001t0013g0036others(7): Show | 12 | HG01975.hp1 HG02451.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.320+161C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583247 | ||||||
chr2:218583249
|
C | G | 11 | a0001c0001t0001g0139a0001c0001t0011g0220a0001c0001t0013g0036others(8): Show | 13 | HG01975.hp1 HG02451.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.320+163C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583249 | ||||||
chr2:218583251
|
C | G | 8 | a0001c0001t0011g0220a0001c0001t0013g0156a0001c0001t0018g0151others(5): Show | 9 | HG01975.hp1 HG02451.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.320+165C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583251 | ||||||
chr2:218583253
|
C | G | 5 | a0001c0001t0018g0150a0001c0001t0018g0151a0001c0001t0024g0115others(2): Show | 5 | HG01975.hp1 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+167C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583253 | ||||||
chr2:218583255
|
C | G | 3 | a0001c0001t0018g0150a0001c0001t0018g0151a0001c0001t0024g0153 | 3 | HG02723.hp1 HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.320+169C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583255 | ||||||
chr2:218583257
|
C | G | 4 | a0001c0001t0002g0083a0001c0001t0018g0150a0001c0001t0018g0151others(1): Show | 4 | HG02723.hp1 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.320+171C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583257 | ||||||
chr2:218583265
|
C | T | 1 | a0001c0001t0013g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.320+179C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583265 | ||||||
chr2:218583286
|
TC | T | 3 | a0001c0001t0001g0141a0001c0001t0004g0205a0001c0001t0010g0209 | 3 | HG01175.hp1 NA19012.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.320+202delC | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583286 | |||||
chr2:218583842
|
G | A | 2 | a0001c0001t0012g0009a0001c0001t0012g0161 | 5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.320+756G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583842 | ||||||
chr2:218584139
|
G | T | 11 | a0001c0001t0014g0017a0001c0001t0014g0167a0001c0001t0014g0176others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.321-473G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218584139 | ||||||
chr2:218584294
|
G | A | 3 | a0001c0001t0004g0200a0001c0001t0004g0205a0001c0001t0010g0203 | 3 | HG02074.hp2 NA18981.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.321-318G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218584294 | ||||||
chr2:218584320
|
G | T | 9 | a0001c0001t0003g0182a0001c0001t0003g0184a0001c0001t0003g0187others(6): Show | 9 | HG02145.hp1 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.321-292G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218584320 | ||||||
chr2:218584370
|
C | G | 2 | a0001c0001t0007g0159a0001c0001t0007g0160 | 2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.321-242C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218584370 | ||||||
chr2:218584761
|
C | A | 8 | a0001c0001t0009g0037a0001c0001t0009g0164a0001c0001t0015g0037others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+40C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218584761 | ||||||
chr2:218585020
|
G | A | 1 | a0001c0001t0018g0152 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.430+299G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585020 | ||||||
chr2:218585059
|
C | T | 1 | a0001c0001t0003g0066 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.430+338C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585059 | ||||||
chr2:218585166
|
C | G | 1 | a0001c0001t0009g0164 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.430+445C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585166 | ||||||
chr2:218585236
|
GTCTTACT | G | 144 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(141): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.430+519_430+525del others(7): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 218585236 | |||||
chr2:218585366
|
C | T | 242 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(239): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.430+645C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585366 | ||||||
chr2:218585574
|
C | CA | 177 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(174): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.430+865dupA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 218585574 | |||||
chr2:218585641
|
T | TTA | 194 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0139others(191): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.430+921_430+922ins others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 218585641 | |||||
chr2:218585642
|
T | TTTA | 42 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(39): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.430+923_430+924ins others(3): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 218585642 | |||||
chr2:218585643
|
T | A | 2 | a0001c0001t0007g0159a0001c0001t0007g0160 | 2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.430+922T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585643 | ||||||
chr2:218585645
|
T | A | 2 | a0001c0001t0012g0009a0001c0001t0012g0161 | 5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+924T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585645 | ||||||
chr2:218585646
|
T | A | 144 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(141): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.430+925T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585646 | ||||||
chr2:218585647
|
T | A | 1 | a0001c0001t0002g0074 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.430+926T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585647 | ||||||
chr2:218585651
|
T | A | 2 | a0001c0001t0003g0090a0001c0001t0004g0200 | 2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.430+930T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585651 | ||||||
chr2:218585663
|
A | G | 1 | a0001c0001t0006g0172 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.430+942A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585663 | ||||||
chr2:218585824
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.430+1103G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585824 | ||||||
chr2:218585873
|
C | T | 34 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(31): Show | 46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.430+1152C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585873 | ||||||
chr2:218585892
|
T | G | 2 | a0001c0001t0043g0191a0001c0001t0044g0180 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.430+1171T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585892 | ||||||
chr2:218586164
|
A | G | 5 | a0001c0001t0018g0150a0001c0001t0018g0151a0001c0001t0018g0152others(2): Show | 6 | HG02723.hp1 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-1422A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218586164 | ||||||
chr2:218586292
|
T | G | 102 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(99): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.431-1294T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218586292 | ||||||
chr2:218586313
|
A | G | 2 | a0001c0001t0019g0168a0001c0001t0019g0169 | 2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.431-1273A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218586313 | ||||||
chr2:218586339
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.431-1247G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218586339 | ||||||
chr2:218586488
|
C | CT | 23 | a0001c0001t0001g0132a0001c0001t0002g0095a0001c0001t0003g0027others(20): Show | 24 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.431-1082dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 218586488 | |||||
chr2:218586650
|
G | A | 2 | a0001c0001t0012g0009a0001c0001t0012g0161 | 5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-936G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218586650 | ||||||
chr2:218586687
|
C | T | 7 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0073others(4): Show | 14 | HG01070.hp1 HG02071.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.431-899C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218586687 | ||||||
chr2:218587051
|
T | C | 11 | a0001c0001t0014g0017a0001c0001t0014g0167a0001c0001t0014g0176others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.431-535T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218587051 | ||||||
chr2:218587191
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(239): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.431-395A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218587191 | ||||||
chr2:218587311
|
C | T | 1 | a0001c0001t0018g0152 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.431-275C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218587311 | ||||||
chr2:218587427
|
CT | C | 18 | a0001c0001t0003g0048a0001c0001t0003g0068a0001c0001t0003g0182others(15): Show | 18 | HG01109.hp1 HG01884.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.431-148delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 218587427 | |||||
chr2:218587774
|
T | C | 6 | a0001c0001t0009g0037a0001c0001t0009g0164a0001c0001t0015g0037others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+79T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218587774 | ||||||
chr2:218588053
|
C | A | 1 | a0001c0001t0054g0117 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.540+358C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588053 | ||||||
chr2:218588202
|
T | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0134a0001c0001t0001g0137 | 3 | NA19055.hp2 NA19074.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.540+507T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588202 | ||||||
chr2:218588287
|
C | CTTTTTT | 33 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(30): Show | 45 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(42): Show |
intron_variant | MODIFIER | c.540+602_540+607dup others(6): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588287 | |||||
chr2:218588374
|
C | T | 102 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(99): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.540+679C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588374 | ||||||
chr2:218588407
|
G | C | 1 | a0001c0001t0001g0135 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.540+712G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588407 | ||||||
chr2:218588415
|
A | G | 15 | a0001c0001t0003g0182a0001c0001t0003g0184a0001c0001t0003g0187others(12): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.540+720A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588415 | ||||||
chr2:218588434
|
A | G | 102 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(99): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.540+739A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588434 | ||||||
chr2:218588512
|
C | A | 9 | a0001c0001t0013g0036a0001c0001t0013g0154a0001c0001t0013g0155others(6): Show | 11 | HG02723.hp1 HG02886.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.540+817C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588512 | ||||||
chr2:218588513
|
C | T | 180 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(177): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.540+818C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588513 | ||||||
chr2:218588588
|
C | CT | 10 | a0001c0001t0007g0159a0001c0001t0009g0037a0001c0001t0014g0167others(7): Show | 10 | HG02257.hp1 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.540+919dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | |||||
chr2:218588588
|
C | CTTT | 8 | a0001c0001t0002g0097a0001c0001t0003g0044a0001c0001t0005g0070others(5): Show | 11 | HG00099.hp2 HG02717.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.540+917_540+919dup others(3): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | |||||
chr2:218588588
|
C | CTTTT | 66 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(63): Show | 92 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.540+916_540+919dup others(4): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | |||||
chr2:218588588
|
C | CTTTTT | 36 | a0001c0001t0002g0007a0001c0001t0002g0026a0001c0001t0002g0063others(33): Show | 44 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.540+915_540+919dup others(5): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | |||||
chr2:218588588
|
C | CTTTTTT | 7 | a0001c0001t0002g0029a0001c0001t0006g0166a0001c0001t0006g0171others(4): Show | 8 | HG02257.hp2 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.540+914_540+919dup others(6): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | |||||
chr2:218588588
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0004g0199a0001c0001t0013g0154 | 2 | HG02083.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.540+909_540+919dup others(11): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | |||||
chr2:218588588
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0004g0201a0001c0001t0004g0206a0001c0001t0018g0151others(1): Show | 4 | HG00558.hp2 HG02896.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+908_540+919dup others(12): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | |||||
chr2:218588588
|
C | CTTTTTTT others(6): Show |
18 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0038others(15): Show | 25 | HG00621.hp1 HG02165.hp2 HG02723.hp1 others(22): Show |
intron_variant | MODIFIER | c.540+907_540+919dup others(13): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | |||||
chr2:218588588
|
C | CTTTTTTT others(7): Show |
15 | a0001c0001t0004g0020a0001c0001t0004g0039a0001c0001t0004g0041others(12): Show | 20 | HG02027.hp2 HG02074.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.540+906_540+919dup others(14): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | |||||
chr2:218588588
|
C | CTTTTTTT others(8): Show |
3 | a0001c0001t0004g0040a0001c0001t0004g0213a0001c0001t0004g0217 | 4 | HG02135.hp2 NA18952.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+905_540+919dup others(15): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | |||||
chr2:218588588
|
CTT | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(42): Show | 69 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.540+918_540+919del others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | |||||
chr2:218588588
|
CTTTT | C | 14 | a0001c0001t0003g0182a0001c0001t0003g0184a0001c0001t0003g0187others(11): Show | 14 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.540+916_540+919del others(4): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | |||||
chr2:218588604
|
T | G | 1 | a0001c0001t0041g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.540+909T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588604 | ||||||
chr2:218588633
|
C | T | 36 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(33): Show | 51 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(48): Show |
intron_variant | MODIFIER | c.540+938C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588633 | ||||||
chr2:218588733
|
A | AT | 96 | a0001c0001t0001g0125a0001c0001t0002g0001a0001c0001t0002g0003others(93): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.540+1051dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588733 | |||||
chr2:218588733
|
A | ATT | 5 | a0001c0001t0002g0030a0001c0001t0002g0104a0001c0001t0003g0110others(2): Show | 6 | HG02698.hp2 NA18950.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+1050_540+1051d others(4): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588733 | |||||
chr2:218589156
|
T | C | 36 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(33): Show | 51 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(48): Show |
intron_variant | MODIFIER | c.540+1461T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589156 | ||||||
chr2:218589387
|
C | T | 2 | a0001c0001t0012g0009a0001c0001t0012g0161 | 5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+1692C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589387 | ||||||
chr2:218589565
|
G | A | 1 | a0001c0001t0011g0220 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.540+1870G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589565 | ||||||
chr2:218589688
|
G | GTAGCCAC others(10): Show |
1 | a0001c0001t0031g0081 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.540+1994_540+1995i others(19): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218589688 | |||||
chr2:218589763
|
C | G | 1 | a0001c0001t0002g0028 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.540+2068C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589763 | ||||||
chr2:218589806
|
T | C | 34 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(31): Show | 46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.540+2111T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589806 | ||||||
chr2:218589946
|
A | G | 1 | a0001c0001t0026g0179 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.540+2251A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589946 | ||||||
chr2:218589947
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.540+2252C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589947 | ||||||
chr2:218590051
|
T | A | 1 | a0001c0001t0005g0188 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.541-2253T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590051 | ||||||
chr2:218590054
|
GT | G | 141 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(138): Show | 176 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.541-2239delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218590054 | |||||
chr2:218590060
|
T | G | 6 | a0001c0001t0009g0037a0001c0001t0009g0164a0001c0001t0015g0037others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-2244T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590060 | ||||||
chr2:218590063
|
T | G | 15 | a0001c0001t0001g0125a0001c0001t0002g0028a0001c0001t0002g0077others(12): Show | 16 | HG01258.hp1 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.541-2241T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590063 | ||||||
chr2:218590063
|
T | TTG | 35 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(32): Show | 50 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(47): Show |
intron_variant | MODIFIER | c.541-2240_541-2239i others(4): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218590063 | |||||
chr2:218590078
|
T | G | 180 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(177): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.541-2226T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590078 | ||||||
chr2:218590234
|
A | T | 1 | a0001c0001t0009g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.541-2070A>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590234 | ||||||
chr2:218590448
|
G | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(239): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.541-1856G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590448 | ||||||
chr2:218590664
|
T | C | 11 | a0001c0001t0014g0017a0001c0001t0014g0167a0001c0001t0014g0176others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-1640T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590664 | ||||||
chr2:218590797
|
C | CTTG | 5 | a0001c0001t0004g0201a0001c0001t0012g0009a0001c0001t0012g0161others(2): Show | 8 | HG00558.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.541-1483_541-1481d others(5): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218590797 | |||||
chr2:218590797
|
C | CTTGTTG | 33 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0020others(30): Show | 45 | HG00621.hp1 HG02027.hp2 HG02074.hp2 others(42): Show |
intron_variant | MODIFIER | c.541-1486_541-1481d others(8): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218590797 | |||||
chr2:218590797
|
CTTG | C | 117 | a0001c0001t0001g0145a0001c0001t0002g0001a0001c0001t0002g0003others(114): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.541-1483_541-1481d others(5): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218590797 | |||||
chr2:218590797
|
CTTGTTG | C | 8 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0166others(5): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.541-1486_541-1481d others(8): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218590797 | |||||
chr2:218590811
|
T | C | 1 | a0001c0001t0022g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.541-1493T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590811 | ||||||
chr2:218590865
|
G | A | 1 | a0001c0001t0004g0202 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.541-1439G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590865 | ||||||
chr2:218591052
|
G | A | 11 | a0001c0001t0014g0017a0001c0001t0014g0167a0001c0001t0014g0176others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-1252G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591052 | ||||||
chr2:218591166
|
A | G | 1 | a0001c0001t0002g0067 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.541-1138A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591166 | ||||||
chr2:218591244
|
G | T | 102 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(99): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.541-1060G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591244 | ||||||
chr2:218591252
|
A | G | 2 | a0001c0001t0012g0009a0001c0001t0012g0161 | 5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-1052A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591252 | ||||||
chr2:218591549
|
C | A | 1 | a0001c0001t0007g0128 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.541-755C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591549 | ||||||
chr2:218591613
|
G | A | 2 | a0001c0001t0002g0061a0001c0001t0002g0107 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.541-691G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591613 | ||||||
chr2:218591618
|
C | T | 1 | a0001c0001t0048g0216 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.541-686C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591618 | ||||||
chr2:218591694
|
A | G | 180 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(177): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.541-610A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591694 | ||||||
chr2:218592006
|
C | T | 6 | a0001c0001t0009g0037a0001c0001t0009g0164a0001c0001t0015g0037others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-298C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592006 | ||||||
chr2:218592014
|
A | G | 144 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(141): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.541-290A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592014 | ||||||
chr2:218592047
|
C | T | 1 | a0001c0001t0048g0216 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.541-257C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592047 | ||||||
chr2:218592082
|
C | T | 2 | a0001c0001t0002g0079a0001c0001t0002g0080 | 2 | HG00438.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.541-222C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592082 | ||||||
chr2:218592122
|
G | A | 3 | a0001c0001t0014g0167a0001c0001t0019g0168a0001c0001t0019g0169 | 3 | HG02630.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.541-182G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592122 | ||||||
chr2:218592141
|
A | G | 2 | a0001c0001t0012g0009a0001c0001t0012g0161 | 5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-163A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592141 | ||||||
chr2:218592186
|
A | C | 1 | a0001c0001t0003g0078 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.541-118A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592186 | ||||||
chr2:218592226
|
T | G | 1 | a0001c0001t0003g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.541-78T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592226 | ||||||
chr2:218592471
|
A | G | 1 | a0001c0001t0005g0031 | 2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.639+69A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 6/7 | chr2 | 218592471 | ||||||
chr2:218592535
|
A | G | 1 | a0001c0001t0003g0027 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.640-81A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 6/7 | chr2 | 218592535 | ||||||
chr2:218592946
|
G | A | 1 | a0001c0001t0035g0062 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.731+239G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218592946 | ||||||
chr2:218593008
|
C | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(46): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.731+301C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593008 | ||||||
chr2:218593018
|
G | A | 180 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(177): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.731+311G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593018 | ||||||
chr2:218593152
|
TTC | T | 5 | a0001c0001t0022g0018a0001c0001t0022g0189a0001c0001t0027g0018others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.731+447_731+448del others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 218593152 | |||||
chr2:218593472
|
A | G | 1 | a0001c0001t0002g0073 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.732-636A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593472 | ||||||
chr2:218593631
|
C | T | 2 | a0001c0001t0002g0021a0001c0001t0003g0021 | 2 | HG01255.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.732-477C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593631 | ||||||
chr2:218593775
|
T | A | 4 | a0001c0001t0018g0150a0001c0001t0018g0151a0001c0001t0018g0152others(1): Show | 4 | HG02723.hp1 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.732-333T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593775 | ||||||
chr2:218593899
|
G | A | 1 | a0001c0001t0008g0065 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.732-209G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593899 | ||||||
chr2:218593933
|
T | C | 144 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(141): Show | 179 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.732-175T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593933 | ||||||
chr2:218593981
|
G | T | 2 | a0001c0001t0003g0192a0001c0001t0005g0193 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.732-127G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593981 | ||||||
chr2:218594084
|
T | C | 2 | a0001c0001t0003g0192a0001c0001t0005g0193 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.732-24T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218594084 |