geneid | 26504 |
---|---|
ensemblid | ENSG00000158158.12 |
hgncid | 105 |
symbol | CNNM4 |
name | cyclin and CBS domain divalent metal cation transport mediator 4 |
refseq_nuc | NM_020184.4 |
refseq_prot | NP_064569.3 |
ensembl_nuc | ENST00000377075.3 |
ensembl_prot | ENSP00000366275.2 |
mane_status | MANE Select |
chr | chr2 |
start | 96760902 |
end | 96811874 |
strand | + |
ver | v1.2 |
region | chr2:96760902-96811874 |
region5000 | chr2:96755902-96816874 |
regionname0 | CNNM4_chr2_96760902_96811874 |
regionname5000 | CNNM4_chr2_96755902_96816874 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 775 | 265 | 84 | 55 | 94 | 12 | 18 | 68 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0002 | 0/0 | 775 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0003 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0004 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0005 | 0/0 | 775 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2328 | 252 | 74 | 53 | 93 | 12 | 18 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
c0002 | 0/0 | 2328 | 9 | 9 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
c0003 | 0/0 | 2328 | 2 | 0 | 2 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
c0004 | 0/0 | 2328 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
c0005 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
c0006 | 0/0 | 2328 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
c0007 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
c0008 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
c0009 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2456 | 149 | 10 | 43 | 69 | 11 | 14 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0002 | 0/0 | 2456 | 39 | 21 | 2 | 14 | 0 | 2 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0003 | 0/0 | 2456 | 29 | 10 | 9 | 9 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0004 | 0/0 | 2456 | 19 | 19 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0005 | 0/0 | 2456 | 13 | 13 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0006 | 0/0 | 2456 | 8 | 7 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0007 | 0/0 | 2456 | 4 | 4 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0008 | 0/0 | 2453 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0009 | 0/0 | 2456 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0010 | 0/0 | 2456 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0011 | 0/0 | 2456 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0012 | 0/0 | 2456 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0013 | 0/0 | 2456 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0014 | 0/0 | 2456 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
t0015 | 0/0 | 2456 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2328 | 252 | 74 | 53 | 93 | 12 | 18 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0002 | 0/0 | 2328 | 9 | 9 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0003 | 0/0 | 2328 | 2 | 0 | 2 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0008 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0009 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0002c0004 | 0/0 | 2328 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0003c0005 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0004c0007 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0005c0006 | 0/0 | 2328 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4783 | 146 | 10 | 40 | 69 | 11 | 14 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0002 | 0/0 | 4783 | 37 | 20 | 2 | 13 | 0 | 2 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0003 | 0/0 | 4783 | 27 | 8 | 9 | 9 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0004 | 0/0 | 4783 | 19 | 19 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0005 | 0/0 | 4783 | 4 | 4 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0006 | 0/0 | 4783 | 7 | 6 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0007 | 0/0 | 4783 | 3 | 3 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0008 | 0/0 | 4780 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0009 | 0/0 | 4783 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0010 | 0/0 | 4783 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0011 | 0/0 | 4783 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0012 | 0/0 | 4783 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0013 | 0/0 | 4783 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0014 | 0/0 | 4783 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0001t0015 | 0/0 | 4783 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0002t0005 | 0/0 | 4783 | 9 | 9 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0003t0001 | 0/0 | 4783 | 2 | 0 | 2 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0008t0002 | 0/0 | 4783 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0001c0009t0007 | 0/0 | 4783 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0002c0004t0003 | 0/0 | 4783 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0003c0005t0006 | 0/0 | 4783 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0004c0007t0002 | 0/0 | 4783 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
a0005c0006t0001 | 0/0 | 4783 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | copy fasta | chr2 | 96755902 | 96816874 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0006g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0008g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0009g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0010g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0011g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0012g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0013g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0014g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0001t0015g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0002t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0002t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0002t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0002t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0002t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0002t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0002t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0002t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0002t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0008t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0001c0009t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0002c0004t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0002c0004t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0003c0005t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0004c0007t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
a0005c0006t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | GBR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | GBR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | FIN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0078 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01074 | hp2 | a0005 | c0006 | t0001 | g0255 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01081 | hp1 | a0001 | c0003 | t0001 | g0250 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01175 | hp1 | a0001 | c0001 | t0015 | g0242 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | IBS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01884 | hp2 | a0001 | c0002 | t0005 | g0137 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0076 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02055 | hp1 | a0001 | c0001 | t0012 | g0116 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02145 | hp2 | a0001 | c0009 | t0007 | g0193 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | CDX | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CDX | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CDX | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02257 | hp1 | a0001 | c0002 | t0005 | g0139 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0265 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0188 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0126 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02809 | hp1 | a0002 | c0004 | t0003 | g0102 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02895 | hp2 | a0002 | c0004 | t0003 | g0103 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0029 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0168 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0167 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02922 | hp2 | a0004 | c0007 | t0002 | g0157 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02965 | hp2 | a0001 | c0002 | t0005 | g0135 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0122 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03017 | hp1 | a0001 | c0001 | t0014 | g0098 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0121 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03130 | hp1 | a0001 | c0002 | t0005 | g0144 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03130 | hp2 | a0003 | c0005 | t0006 | g0233 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03139 | hp2 | a0001 | c0002 | t0005 | g0141 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03195 | hp2 | a0001 | c0002 | t0005 | g0074 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03516 | hp2 | a0001 | c0002 | t0005 | g0140 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03579 | hp2 | a0001 | c0002 | t0005 | g0268 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | BEB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0100 | SAS | BEB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | STU | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | STU | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | STU | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | YRI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | YRI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0166 | AFR | YRI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18951 | hp1 | a0001 | c0001 | t0010 | g0127 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18983 | hp2 | a0001 | c0008 | t0002 | g0027 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19030 | hp1 | a0001 | c0001 | t0008 | g0239 | AFR | LWK | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0234 | AFR | LWK | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | LWK | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | LWK | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19064 | hp2 | a0001 | c0001 | t0013 | g0108 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | YRI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0077 | AFR | ASW | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | ASW | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA20752 | hp1 | a0001 | c0001 | t0009 | g0049 | EUR | TSI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | TSI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | TSI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02109 | hp2 | a0001 | c0002 | t0005 | g0136 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | USA | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | USA | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | USA | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | USA | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | LWK | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0192 | REF | REF | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0262 | REF | REF | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:96761547
|
G | C | 1 | a0003 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.548G>C | p.Trp183Ser | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/7 | 646/4783 | 548/2328 | 183/775 | chr2 | 96761547 | ||
chr2:96761787
|
A | G | 1 | a0002 | 2 | HG02809.hp1 HG02895.hp2 |
missense_variant | MODERATE | c.788A>G | p.Asn263Ser | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/7 | 886/4783 | 788/2328 | 263/775 | chr2 | 96761787 | ||
chr2:96799603
|
G | A | 1 | a0005 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.1903G>A | p.Ala635Thr | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/7 | 2001/4783 | 1903/2328 | 635/775 | chr2 | 96799603 | ||
chr2:96809330
|
A | T | 1 | a0004 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.2141A>T | p.Gln714Leu | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 2239/4783 | 2141/2328 | 714/775 | chr2 | 96809330 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:96761962
|
C | T | 1 | a0001c0009 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.963C>T | p.Ser321Ser | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/7 | 1061/4783 | 963/2328 | 321/775 | chr2 | 96761962 | ||
chr2:96762340
|
C | T | 1 | a0001c0009 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1341C>T | p.His447His | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/7 | 1439/4783 | 1341/2328 | 447/775 | chr2 | 96762340 | ||
chr2:96799199
|
G | A | 1 | a0001c0002 | 9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
synonymous_variant | LOW | c.1824G>A | p.Pro608Pro | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 4/7 | 1922/4783 | 1824/2328 | 608/775 | chr2 | 96799199 | ||
chr2:96799602
|
C | T | 1 | a0001c0008 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.1902C>T | p.Gly634Gly | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/7 | 2000/4783 | 1902/2328 | 634/775 | chr2 | 96799602 | ||
chr2:96799647
|
C | T | 1 | a0001c0003 | 2 | HG01081.hp1 HG02300.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1947C>T | p.Ser649Ser | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/7 | 2045/4783 | 1947/2328 | 649/775 | chr2 | 96799647 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:96760946
|
C | T | 1 | a0001c0001t0015 | 1 | HG01175.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-54C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/7 | chr2 | 96760946 | ||||||
chr2:96809608
|
C | T | 3 | a0001c0001t0004a0001c0001t0005a0001c0002t0005 | 32 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*91C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 91 | chr2 | 96809608 | |||||
chr2:96809612
|
T | C | 1 | a0001c0001t0009 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*95T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 95 | chr2 | 96809612 | |||||
chr2:96809975
|
TTCC | T | 1 | a0001c0001t0008 | 2 | HG02970.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*477_*479delTCC | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 477 | INFO_REALIGN_3_PRIME | chr2 | 96809975 | ||||
chr2:96810270
|
G | A | 1 | a0001c0001t0010 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*753G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 753 | chr2 | 96810270 | |||||
chr2:96810482
|
A | G | 4 | a0001c0001t0003a0001c0001t0013a0001c0001t0014others(1): Show | 31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*965A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 965 | chr2 | 96810482 | |||||
chr2:96810576
|
T | C | 1 | a0001c0001t0010 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 1059 | chr2 | 96810576 | |||||
chr2:96810761
|
C | T | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0012others(1): Show | 33 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1244C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 1244 | chr2 | 96810761 | |||||
chr2:96810999
|
C | T | 2 | a0001c0001t0006a0003c0005t0006 | 8 | HG00642.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1482C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 1482 | chr2 | 96810999 | |||||
chr2:96811033
|
C | T | 2 | a0001c0001t0007a0001c0009t0007 | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1516C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 1516 | chr2 | 96811033 | |||||
chr2:96811210
|
G | A | 3 | a0001c0001t0004a0001c0001t0005a0001c0002t0005 | 32 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1693G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 1693 | chr2 | 96811210 | |||||
chr2:96811507
|
T | A | 2 | a0001c0001t0005a0001c0002t0005 | 13 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1990T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 1990 | chr2 | 96811507 | |||||
chr2:96811637
|
C | T | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(11): Show | 113 | HG00609.hp1 HG00642.hp1 HG01070.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2120C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 2120 | chr2 | 96811637 | |||||
chr2:96811842
|
T | C | 1 | a0001c0001t0011 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2325T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 2325 | chr2 | 96811842 | |||||
chr2:96811847
|
T | G | 1 | a0001c0001t0014 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2330T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 2330 | chr2 | 96811847 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:96762583
|
G | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(69): Show | 72 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1402+182G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96762583 | ||||||
chr2:96762638
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1402+237C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96762638 | ||||||
chr2:96762725
|
G | A | 1 | a0001c0002t0005g0074 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1402+324G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96762725 | ||||||
chr2:96762971
|
C | T | 1 | a0001c0002t0005g0268 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1402+570C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96762971 | ||||||
chr2:96763183
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1402+782C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96763183 | ||||||
chr2:96763258
|
G | T | 1 | a0001c0001t0001g0266 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1402+857G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96763258 | ||||||
chr2:96763539
|
G | C | 1 | a0001c0001t0003g0075 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1402+1138G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96763539 | ||||||
chr2:96763549
|
G | A | 2 | a0001c0001t0006g0076a0001c0001t0006g0077 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1402+1148G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96763549 | ||||||
chr2:96763647
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1402+1246C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96763647 | ||||||
chr2:96764196
|
G | C | 3 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0006g0078 | 3 | HG00642.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1402+1795G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96764196 | ||||||
chr2:96764214
|
T | G | 252 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(249): Show | 253 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.1402+1813T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96764214 | ||||||
chr2:96764483
|
CT | C | 9 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1402+2083delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96764483 | ||||||
chr2:96764589
|
G | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG02145.hp1 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402+2188G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96764589 | ||||||
chr2:96764717
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02523.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1402+2316G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96764717 | ||||||
chr2:96765014
|
G | T | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG02071.hp2 HG02165.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1402+2613G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765014 | ||||||
chr2:96765024
|
G | GTT | 6 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0243others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+2664_1402+266 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0006g0246 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1402+2656_1402+266 others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GT | G | 20 | a0001c0001t0001g0071a0001c0001t0001g0220a0001c0001t0001g0221others(17): Show | 20 | HG00280.hp2 HG00673.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1402+2665delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTT | G | 34 | a0001c0001t0001g0008a0001c0001t0001g0191a0001c0001t0001g0192others(31): Show | 34 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.1402+2664_1402+266 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTT | G | 44 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0059others(41): Show | 44 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1402+2663_1402+266 others(7): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTT | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(36): Show | 40 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.1402+2662_1402+266 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTT | G | 22 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(19): Show | 22 | HG00741.hp2 HG01496.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1402+2661_1402+266 others(9): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTTT | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG01123.hp2 HG01975.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+2660_1402+266 others(10): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTTTT others(3): Show |
G | 2 | a0001c0001t0005g0143a0001c0002t0005g0144 | 2 | HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1402+2656_1402+266 others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTTTT others(4): Show |
G | 6 | a0001c0001t0004g0138a0001c0001t0005g0142a0001c0002t0005g0139others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+2655_1402+266 others(15): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTTTT others(5): Show |
G | 13 | a0001c0001t0004g0080a0001c0001t0004g0128a0001c0001t0004g0129others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1402+2654_1402+266 others(16): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTTTT others(6): Show |
G | 8 | a0001c0001t0001g0251a0001c0001t0004g0079a0001c0001t0004g0123others(5): Show | 8 | HG00642.hp1 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1402+2653_1402+266 others(17): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTTTT others(7): Show |
G | 3 | a0001c0001t0004g0119a0001c0001t0004g0120a0001c0001t0004g0121 | 3 | HG02486.hp1 HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1402+2652_1402+266 others(18): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTTTT others(8): Show |
G | 2 | a0001c0001t0004g0117a0001c0001t0004g0118 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1402+2651_1402+266 others(19): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTTTT others(9): Show |
G | 2 | a0001c0001t0001g0009a0001c0001t0012g0116 | 2 | HG00642.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1402+2650_1402+266 others(20): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTTTT others(11): Show |
G | 1 | a0001c0003t0001g0250 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1402+2648_1402+266 others(22): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTTTT others(12): Show |
G | 8 | a0001c0001t0002g0115a0001c0001t0003g0089a0001c0001t0003g0109others(5): Show | 8 | HG01071.hp2 HG01981.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1402+2647_1402+266 others(23): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTTTT others(13): Show |
G | 24 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(21): Show | 24 | HG01070.hp2 HG01099.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1402+2646_1402+266 others(24): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTTTT others(14): Show |
G | 1 | a0001c0001t0001g0093 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1402+2645_1402+266 others(25): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765024
|
GTTTTTTT others(19): Show |
G | 3 | a0001c0001t0005g0092a0001c0001t0006g0076a0001c0001t0006g0077 | 3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1402+2640_1402+266 others(30): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | |||||
chr2:96765032
|
T | G | 1 | a0001c0001t0001g0090 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1402+2631T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765032 | ||||||
chr2:96765037
|
T | G | 1 | a0001c0001t0001g0007 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1402+2636T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765037 | ||||||
chr2:96765038
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1402+2637T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765038 | ||||||
chr2:96765100
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1402+2699C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765100 | ||||||
chr2:96765134
|
T | G | 2 | a0001c0001t0006g0076a0001c0001t0006g0077 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1402+2733T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765134 | ||||||
chr2:96765146
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0191 | 2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1402+2745G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765146 | ||||||
chr2:96765221
|
G | T | 1 | a0001c0001t0013g0108 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1402+2820G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765221 | ||||||
chr2:96765332
|
G | A | 4 | a0001c0001t0006g0234a0001c0001t0006g0235a0001c0001t0006g0246others(1): Show | 4 | HG03130.hp2 HG03195.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402+2931G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765332 | ||||||
chr2:96765372
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1402+2971C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765372 | ||||||
chr2:96765424
|
C | A | 31 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1402+3023C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765424 | ||||||
chr2:96765489
|
C | T | 1 | a0001c0001t0005g0142 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1402+3088C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765489 | ||||||
chr2:96765662
|
A | G | 12 | a0001c0001t0005g0126a0001c0001t0005g0142a0001c0001t0005g0143others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1402+3261A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765662 | ||||||
chr2:96765777
|
TTTTC | T | 44 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(41): Show | 44 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.1402+3396_1402+339 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765777 | |||||
chr2:96766053
|
G | A | 1 | a0001c0001t0008g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1402+3652G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96766053 | ||||||
chr2:96766090
|
T | A | 1 | a0001c0001t0008g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1402+3689T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96766090 | ||||||
chr2:96766144
|
G | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG02145.hp1 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402+3743G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96766144 | ||||||
chr2:96766364
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1402+3963C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96766364 | ||||||
chr2:96766580
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0012g0116 | 3 | HG00280.hp1 HG00323.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1402+4179G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96766580 | ||||||
chr2:96767390
|
G | C | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1402+4989G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96767390 | ||||||
chr2:96767425
|
A | C | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1402+5024A>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96767425 | ||||||
chr2:96767986
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1402+5585C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96767986 | ||||||
chr2:96768098
|
A | G | 1 | a0001c0001t0004g0134 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1402+5697A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96768098 | ||||||
chr2:96768324
|
C | G | 60 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(57): Show | 60 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1402+5923C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96768324 | ||||||
chr2:96768357
|
AG | A | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1402+5957delG | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96768357 | ||||||
chr2:96768548
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1402+6147C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96768548 | ||||||
chr2:96768877
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1402+6476G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96768877 | ||||||
chr2:96769078
|
T | C | 1 | a0001c0001t0008g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1402+6677T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769078 | ||||||
chr2:96769397
|
C | T | 8 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0130others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1402+6996C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769397 | ||||||
chr2:96769457
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1402+7056G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769457 | ||||||
chr2:96769458
|
C | A | 1 | a0001c0001t0001g0165 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1402+7057C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769458 | ||||||
chr2:96769563
|
CA | C | 20 | a0001c0001t0001g0162a0001c0001t0001g0218a0001c0001t0004g0079others(17): Show | 20 | HG00639.hp2 HG00642.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1402+7179delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96769563 | |||||
chr2:96769760
|
TG | T | 11 | a0001c0001t0005g0126a0001c0001t0005g0143a0001c0002t0005g0074others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+7360delG | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769760 | ||||||
chr2:96769782
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1402+7381A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769782 | ||||||
chr2:96769788
|
G | A | 1 | a0001c0001t0001g0192 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1402+7387G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769788 | ||||||
chr2:96769813
|
G | A | 2 | a0001c0001t0006g0246a0003c0005t0006g0233 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1402+7412G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769813 | ||||||
chr2:96769820
|
G | A | 31 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1402+7419G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769820 | ||||||
chr2:96770149
|
A | T | 1 | a0001c0001t0012g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1402+7748A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770149 | ||||||
chr2:96770310
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1402+7909C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770310 | ||||||
chr2:96770471
|
G | A | 3 | a0001c0001t0004g0123a0001c0001t0004g0128a0001c0001t0004g0129 | 3 | HG01891.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1402+8070G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770471 | ||||||
chr2:96770532
|
G | A | 2 | a0001c0001t0002g0002a0001c0001t0002g0003 | 2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1402+8131G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770532 | ||||||
chr2:96770555
|
C | G | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1402+8154C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770555 | ||||||
chr2:96770653
|
C | T | 12 | a0001c0001t0005g0126a0001c0001t0005g0142a0001c0001t0005g0143others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1402+8252C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770653 | ||||||
chr2:96770871
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1402+8470C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770871 | ||||||
chr2:96771091
|
A | T | 1 | a0001c0001t0001g0217 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1402+8690A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771091 | ||||||
chr2:96771144
|
C | A | 1 | a0001c0001t0008g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1402+8743C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771144 | ||||||
chr2:96771193
|
G | A | 4 | a0001c0001t0007g0166a0001c0001t0007g0167a0001c0001t0007g0168others(1): Show | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1402+8792G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771193 | ||||||
chr2:96771272
|
ATT | A | 27 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0123others(24): Show | 27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1402+8872_1402+887 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771272 | ||||||
chr2:96771275
|
C | A | 27 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0123others(24): Show | 27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1402+8874C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771275 | ||||||
chr2:96771292
|
T | C | 1 | a0005c0006t0001g0255 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1402+8891T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771292 | ||||||
chr2:96771293
|
CT | C | 8 | a0001c0001t0001g0169a0001c0001t0004g0117a0001c0001t0004g0118others(5): Show | 8 | HG00323.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1402+8907delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96771293 | |||||
chr2:96771475
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1402+9074C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771475 | ||||||
chr2:96771610
|
A | G | 1 | a0001c0001t0002g0067 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1402+9209A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771610 | ||||||
chr2:96771713
|
C | CA | 41 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0194others(38): Show | 41 | HG00423.hp2 HG01070.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1402+9326dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96771713 | |||||
chr2:96772059
|
C | T | 1 | a0001c0001t0006g0188 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1402+9658C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772059 | ||||||
chr2:96772253
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(162): Show | 166 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.1402+9852T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772253 | ||||||
chr2:96772341
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1402+9940C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772341 | ||||||
chr2:96772375
|
GTGCGCAC others(48): Show |
G | 1 | a0001c0001t0010g0127 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1402+9992_1402+100 others(60): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96772375 | |||||
chr2:96772379
|
G | A | 5 | a0001c0001t0001g0170a0001c0001t0001g0194a0001c0001t0001g0195others(2): Show | 5 | HG00423.hp2 NA18612.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1402+9978G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772379 | ||||||
chr2:96772427
|
C | G | 1 | a0001c0001t0008g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1402+10026C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772427 | ||||||
chr2:96772474
|
G | A | 27 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0123others(24): Show | 27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1402+10073G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772474 | ||||||
chr2:96772549
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1402+10148G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772549 | ||||||
chr2:96772609
|
GCACACAC others(57): Show |
G | 3 | a0001c0001t0001g0169a0001c0001t0001g0198a0001c0001t0001g0240 | 3 | HG00323.hp1 HG01106.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1402+10327_1402+10 others(70): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96772609 | |||||
chr2:96772624
|
C | A | 1 | a0001c0001t0012g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1402+10223C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772624 | ||||||
chr2:96772659
|
A | G | 5 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402+10258A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772659 | ||||||
chr2:96772726
|
CGTGCACA others(55): Show |
C | 1 | a0001c0001t0001g0197 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1402+10327_1402+10 others(68): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96772726 | |||||
chr2:96772745
|
A | T | 1 | a0001c0001t0001g0008 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1402+10344A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772745 | ||||||
chr2:96772791
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1402+10390G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772791 | ||||||
chr2:96772815
|
G | C | 60 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(57): Show | 60 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1402+10414G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772815 | ||||||
chr2:96773062
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1402+10661C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773062 | ||||||
chr2:96773261
|
T | G | 1 | a0001c0001t0001g0236 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1402+10860T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773261 | ||||||
chr2:96773264
|
A | T | 156 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(153): Show | 156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1402+10863A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773264 | ||||||
chr2:96773338
|
G | A | 4 | a0001c0001t0001g0252a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG00733.hp1 HG01192.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1402+10937G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773338 | ||||||
chr2:96773488
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1402+11087T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773488 | ||||||
chr2:96773653
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1402+11252G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773653 | ||||||
chr2:96773658
|
C | G | 1 | a0001c0003t0001g0265 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1402+11257C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773658 | ||||||
chr2:96773796
|
TCATGCCA others(8): Show |
T | 1 | a0001c0001t0002g0068 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1402+11398_1402+11 others(21): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96773796 | |||||
chr2:96773819
|
G | T | 1 | a0001c0001t0002g0070 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1402+11418G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773819 | ||||||
chr2:96773841
|
T | TA | 6 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0199others(3): Show | 6 | HG01123.hp2 HG01255.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+11458dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96773841 | |||||
chr2:96773841
|
TA | T | 62 | a0001c0001t0001g0031a0001c0001t0001g0173a0001c0001t0001g0187others(59): Show | 62 | HG00558.hp2 HG00642.hp1 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.1402+11458delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96773841 | |||||
chr2:96773899
|
AAAT | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.1402+11501_1402+11 others(9): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96773899 | |||||
chr2:96774090
|
C | T | 12 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0124others(9): Show | 12 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1402+11689C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774090 | ||||||
chr2:96774400
|
C | T | 3 | a0001c0001t0004g0123a0001c0001t0004g0128a0001c0001t0004g0129 | 3 | HG01891.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1402+11999C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774400 | ||||||
chr2:96774428
|
A | T | 3 | a0001c0001t0004g0123a0001c0001t0004g0128a0001c0001t0004g0129 | 3 | HG01891.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1402+12027A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774428 | ||||||
chr2:96774477
|
G | T | 2 | a0001c0001t0002g0005a0001c0001t0002g0006 | 2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1402+12076G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774477 | ||||||
chr2:96774683
|
G | A | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1402+12282G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774683 | ||||||
chr2:96774830
|
G | A | 31 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1402+12429G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774830 | ||||||
chr2:96774960
|
C | CA | 11 | a0001c0001t0001g0038a0001c0001t0001g0171a0001c0001t0001g0174others(8): Show | 11 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+12597dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CA | C | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(61): Show | 64 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1402+12597delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAA | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0018others(49): Show | 53 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1402+12596_1402+12 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAAA | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | NA18612.hp2 NA18957.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+12595_1402+12 others(9): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAAAAA | C | 7 | a0001c0001t0001g0054a0001c0001t0001g0066a0001c0001t0001g0186others(4): Show | 7 | HG02056.hp1 HG02056.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1402+12593_1402+12 others(11): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAAAAAAA | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0192a0001c0001t0001g0216others(15): Show | 18 | HG01123.hp2 HG01261.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1402+12591_1402+12 others(13): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0215a0001c0001t0002g0002a0001c0001t0002g0003others(3): Show | 6 | HG00099.hp1 HG02630.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402+12590_1402+12 others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0003g0081a0001c0001t0003g0094a0001c0001t0003g0095others(6): Show | 9 | HG01123.hp1 HG02257.hp2 NA18906.hp1 others(6): Show |
intron_variant | MODIFIER | c.1402+12589_1402+12 others(15): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAAAAAAA others(3): Show |
C | 23 | a0001c0001t0003g0075a0001c0001t0003g0082a0001c0001t0003g0083others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1402+12588_1402+12 others(16): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAAAAAAA others(4): Show |
C | 11 | a0001c0001t0003g0088a0001c0001t0004g0125a0001c0001t0004g0130others(8): Show | 11 | HG01256.hp2 HG01884.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+12587_1402+12 others(17): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAAAAAAA others(5): Show |
C | 15 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0123others(12): Show | 15 | HG00642.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1402+12586_1402+12 others(18): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0006g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1402+12585_1402+12 others(19): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0267 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1402+12583_1402+12 others(21): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0001g0161a0001c0001t0006g0076 | 2 | HG01891.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1402+12581_1402+12 others(23): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0005g0092a0001c0001t0006g0077 | 2 | HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1402+12580_1402+12 others(24): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774960
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0001g0254 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1402+12579_1402+12 others(25): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | |||||
chr2:96774998
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1402+12597A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774998 | ||||||
chr2:96775529
|
G | A | 252 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(249): Show | 253 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.1402+13128G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96775529 | ||||||
chr2:96775559
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1402+13158C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96775559 | ||||||
chr2:96775592
|
G | C | 1 | a0001c0001t0004g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1402+13191G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96775592 | ||||||
chr2:96775719
|
GTGTTTTG others(4): Show |
G | 1 | a0001c0001t0001g0190 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1402+13336_1402+13 others(17): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96775719 | |||||
chr2:96775721
|
G | GTTTTGTT others(10): Show |
1 | a0005c0006t0001g0255 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1402+13338_1402+13 others(23): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96775721 | |||||
chr2:96775788
|
T | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG00558.hp1 NA18747.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+13387T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96775788 | ||||||
chr2:96775906
|
A | G | 156 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(153): Show | 156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1402+13505A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96775906 | ||||||
chr2:96776027
|
G | GT | 24 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0061others(21): Show | 24 | HG00423.hp2 HG00673.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.1402+13645dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96776027 | |||||
chr2:96776027
|
GT | G | 5 | a0001c0001t0001g0177a0001c0001t0001g0182a0001c0001t0001g0196others(2): Show | 5 | HG00544.hp1 HG03017.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402+13645delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96776027 | |||||
chr2:96776107
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1402+13706C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96776107 | ||||||
chr2:96776177
|
A | G | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1402+13776A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96776177 | ||||||
chr2:96776307
|
C | T | 2 | a0001c0001t0002g0062a0001c0001t0002g0115 | 2 | HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1402+13906C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96776307 | ||||||
chr2:96776345
|
T | A | 1 | a0001c0001t0008g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1402+13944T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96776345 | ||||||
chr2:96776653
|
G | A | 32 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(29): Show | 32 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1402+14252G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96776653 | ||||||
chr2:96776992
|
A | G | 1 | a0001c0001t0002g0057 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1402+14591A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96776992 | ||||||
chr2:96777042
|
C | T | 1 | a0001c0001t0012g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1402+14641C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777042 | ||||||
chr2:96777081
|
C | T | 31 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1402+14680C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777081 | ||||||
chr2:96777107
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0223 | 2 | NA18962.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1402+14706G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777107 | ||||||
chr2:96777169
|
C | T | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1402+14768C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777169 | ||||||
chr2:96777246
|
C | G | 1 | a0001c0001t0006g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1402+14845C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777246 | ||||||
chr2:96777265
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1402+14864C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777265 | ||||||
chr2:96777387
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1402+14986C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777387 | ||||||
chr2:96777661
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1402+15260C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777661 | ||||||
chr2:96777662
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 5 | HG03225.hp2 NA18522.hp2 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1402+15261G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777662 | ||||||
chr2:96777807
|
T | C | 2 | a0001c0001t0004g0130a0001c0001t0004g0138 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1402+15406T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777807 | ||||||
chr2:96778176
|
T | G | 11 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0124others(8): Show | 11 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+15775T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96778176 | ||||||
chr2:96778556
|
CA | C | 30 | a0001c0001t0001g0257a0001c0001t0002g0159a0001c0001t0004g0079others(27): Show | 30 | HG00642.hp1 HG01261.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1402+16171delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96778556 | |||||
chr2:96778695
|
T | TC | 88 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(85): Show | 88 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1402+16296dupC | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96778695 | |||||
chr2:96778801
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1402+16400C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96778801 | ||||||
chr2:96778837
|
T | C | 11 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0124others(8): Show | 11 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+16436T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96778837 | ||||||
chr2:96778863
|
A | G | 1 | a0001c0001t0005g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1402+16462A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96778863 | ||||||
chr2:96778987
|
C | T | 3 | a0001c0001t0005g0092a0001c0001t0006g0076a0001c0001t0006g0077 | 3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1402+16586C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96778987 | ||||||
chr2:96779236
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1402+16835G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96779236 | ||||||
chr2:96779352
|
T | C | 2 | a0001c0001t0003g0082a0001c0001t0003g0089 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1402+16951T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96779352 | ||||||
chr2:96779508
|
C | CA | 38 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0059others(35): Show | 38 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1402+17129dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96779508 | |||||
chr2:96779508
|
C | CAA | 23 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0085others(20): Show | 23 | HG01099.hp1 HG01168.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1402+17128_1402+17 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96779508 | |||||
chr2:96779508
|
C | CAAA | 11 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(8): Show | 11 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+17127_1402+17 others(9): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96779508 | |||||
chr2:96779508
|
CA | C | 13 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0001t0001g0249others(10): Show | 13 | HG00323.hp1 HG02630.hp2 HG03453.hp2 others(10): Show |
intron_variant | MODIFIER | c.1402+17129delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96779508 | |||||
chr2:96779806
|
AT | A | 32 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(29): Show | 32 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1403-17190delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96779806 | |||||
chr2:96779917
|
C | G | 3 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006 | 3 | HG02145.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1403-17095C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96779917 | ||||||
chr2:96779949
|
C | T | 5 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-17063C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96779949 | ||||||
chr2:96779990
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1403-17022C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96779990 | ||||||
chr2:96780137
|
T | C | 1 | a0001c0001t0002g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1403-16875T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96780137 | ||||||
chr2:96780419
|
CT | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0174others(3): Show | 6 | HG02897.hp1 HG03017.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1403-16576delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96780419 | |||||
chr2:96780506
|
C | T | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-16506C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96780506 | ||||||
chr2:96780905
|
A | AT | 13 | a0001c0001t0001g0269a0001c0001t0002g0145a0001c0001t0002g0146others(10): Show | 13 | HG01261.hp2 HG01358.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.1403-16094dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96780905 | |||||
chr2:96780966
|
C | T | 15 | a0001c0001t0004g0123a0001c0001t0004g0128a0001c0001t0004g0129others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1403-16046C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96780966 | ||||||
chr2:96780972
|
C | CT | 28 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0050others(25): Show | 28 | HG00423.hp1 HG00423.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1403-16016dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96780972 | |||||
chr2:96780972
|
CT | C | 10 | a0001c0001t0001g0045a0001c0001t0001g0060a0001c0001t0001g0093others(7): Show | 10 | HG00558.hp1 HG01070.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1403-16016delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96780972 | |||||
chr2:96781022
|
A | G | 1 | a0004c0007t0002g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1403-15990A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96781022 | ||||||
chr2:96781118
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0223 | 2 | NA18962.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1403-15894A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96781118 | ||||||
chr2:96781269
|
G | A | 5 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-15743G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96781269 | ||||||
chr2:96781356
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1403-15656A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96781356 | ||||||
chr2:96781384
|
C | G | 31 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1403-15628C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96781384 | ||||||
chr2:96781566
|
C | A | 2 | a0001c0001t0001g0253a0005c0006t0001g0255 | 2 | HG00280.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1403-15446C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96781566 | ||||||
chr2:96782094
|
T | A | 157 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(154): Show | 157 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.1403-14918T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782094 | ||||||
chr2:96782318
|
G | A | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-14694G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782318 | ||||||
chr2:96782336
|
T | C | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-14676T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782336 | ||||||
chr2:96782390
|
C | T | 60 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(57): Show | 60 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1403-14622C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782390 | ||||||
chr2:96782411
|
C | CA | 29 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0171others(26): Show | 29 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1403-14585dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96782411 | |||||
chr2:96782545
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 5 | HG03225.hp2 NA18522.hp2 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1403-14467G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782545 | ||||||
chr2:96782640
|
A | G | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-14372A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782640 | ||||||
chr2:96782737
|
G | T | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-14275G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782737 | ||||||
chr2:96782864
|
G | A | 2 | a0001c0001t0002g0222a0001c0001t0002g0237 | 2 | HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1403-14148G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782864 | ||||||
chr2:96782871
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1403-14141G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782871 | ||||||
chr2:96783197
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1403-13815C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96783197 | ||||||
chr2:96783438
|
C | T | 1 | a0001c0001t0006g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1403-13574C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96783438 | ||||||
chr2:96783785
|
A | G | 5 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-13227A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96783785 | ||||||
chr2:96784025
|
A | C | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-12987A>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96784025 | ||||||
chr2:96784597
|
T | G | 3 | a0001c0001t0004g0118a0001c0001t0004g0119a0001c0001t0004g0121 | 3 | HG02486.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1403-12415T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96784597 | ||||||
chr2:96784615
|
C | G | 3 | a0001c0001t0005g0092a0001c0001t0006g0076a0001c0001t0006g0077 | 3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1403-12397C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96784615 | ||||||
chr2:96784772
|
T | C | 28 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0118others(25): Show | 28 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1403-12240T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96784772 | ||||||
chr2:96785227
|
A | G | 2 | a0001c0001t0004g0130a0001c0001t0004g0138 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1403-11785A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96785227 | ||||||
chr2:96785237
|
CT | C | 27 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0123others(24): Show | 27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1403-11766delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96785237 | |||||
chr2:96785630
|
T | C | 1 | a0001c0001t0004g0124 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1403-11382T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96785630 | ||||||
chr2:96785663
|
G | T | 1 | a0001c0001t0006g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1403-11349G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96785663 | ||||||
chr2:96785708
|
G | A | 1 | a0001c0001t0005g0142 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1403-11304G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96785708 | ||||||
chr2:96786255
|
A | G | 2 | a0001c0001t0003g0106a0001c0001t0013g0108 | 2 | HG02155.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1403-10757A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96786255 | ||||||
chr2:96786363
|
A | G | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-10649A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96786363 | ||||||
chr2:96786374
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1403-10638A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96786374 | ||||||
chr2:96786413
|
C | CA | 37 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0172others(34): Show | 37 | HG00609.hp2 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1403-10584dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96786413 | |||||
chr2:96786413
|
CA | C | 17 | a0001c0001t0001g0058a0001c0001t0001g0169a0001c0001t0001g0232others(14): Show | 17 | HG00323.hp1 HG01496.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1403-10584delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96786413 | |||||
chr2:96786507
|
G | A | 3 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0088 | 3 | HG01099.hp1 HG01256.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1403-10505G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96786507 | ||||||
chr2:96786679
|
C | T | 8 | a0001c0001t0002g0062a0001c0001t0002g0064a0001c0001t0002g0067others(5): Show | 8 | HG00609.hp1 HG02056.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1403-10333C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96786679 | ||||||
chr2:96786778
|
C | CA | 24 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0198others(21): Show | 24 | HG00741.hp1 HG01106.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1403-10208dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96786778 | |||||
chr2:96786778
|
CA | C | 78 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(75): Show | 78 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1403-10208delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96786778 | |||||
chr2:96787003
|
T | C | 1 | a0001c0001t0004g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1403-10009T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96787003 | ||||||
chr2:96787100
|
A | G | 2 | a0001c0001t0002g0222a0001c0001t0002g0237 | 2 | HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1403-9912A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96787100 | ||||||
chr2:96787248
|
A | G | 1 | a0001c0001t0002g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1403-9764A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96787248 | ||||||
chr2:96787579
|
C | T | 3 | a0001c0001t0005g0092a0001c0001t0006g0076a0001c0001t0006g0077 | 3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1403-9433C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96787579 | ||||||
chr2:96787659
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1403-9353A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96787659 | ||||||
chr2:96788166
|
G | T | 1 | a0001c0001t0012g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1403-8846G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96788166 | ||||||
chr2:96788252
|
C | CT | 11 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0248others(8): Show | 11 | HG02071.hp2 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1403-8743dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96788252 | |||||
chr2:96788386
|
C | T | 5 | a0001c0001t0001g0170a0001c0001t0001g0194a0001c0001t0001g0195others(2): Show | 5 | HG00423.hp2 NA18612.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1403-8626C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96788386 | ||||||
chr2:96788718
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1403-8294C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96788718 | ||||||
chr2:96788818
|
CCTT | C | 5 | a0001c0001t0003g0095a0001c0001t0003g0097a0001c0001t0003g0105others(2): Show | 5 | NA18950.hp2 NA19054.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1403-8190_1403-818 others(7): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96788818 | |||||
chr2:96788913
|
T | G | 156 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(153): Show | 156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1403-8099T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96788913 | ||||||
chr2:96788968
|
C | T | 156 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(153): Show | 156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1403-8044C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96788968 | ||||||
chr2:96788984
|
CT | C | 60 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(57): Show | 60 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1403-8021delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96788984 | |||||
chr2:96789333
|
G | A | 1 | a0001c0001t0003g0109 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1403-7679G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789333 | ||||||
chr2:96789452
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1403-7560C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789452 | ||||||
chr2:96789479
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | HG00642.hp2 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1403-7533C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789479 | ||||||
chr2:96789539
|
G | A | 2 | a0001c0003t0001g0250a0001c0003t0001g0265 | 2 | HG01081.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1403-7473G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789539 | ||||||
chr2:96789574
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1403-7438C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789574 | ||||||
chr2:96789700
|
A | AT | 7 | a0001c0001t0003g0075a0001c0001t0003g0104a0001c0001t0003g0111others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1403-7298dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96789700 | |||||
chr2:96789841
|
C | T | 1 | a0001c0001t0008g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1403-7171C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789841 | ||||||
chr2:96789877
|
G | C | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG02071.hp2 HG02165.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1403-7135G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789877 | ||||||
chr2:96789881
|
C | T | 14 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0003g0097others(11): Show | 14 | HG01981.hp2 HG02155.hp2 HG03017.hp1 others(11): Show |
intron_variant | MODIFIER | c.1403-7131C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789881 | ||||||
chr2:96789913
|
G | C | 1 | a0001c0001t0005g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1403-7099G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789913 | ||||||
chr2:96789978
|
C | T | 50 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.1403-7034C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789978 | ||||||
chr2:96790003
|
A | AT | 30 | a0001c0001t0001g0010a0001c0001t0001g0066a0001c0001t0001g0164others(27): Show | 30 | HG00639.hp2 HG00673.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1403-6986dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96790003 | |||||
chr2:96790003
|
AT | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0045others(6): Show | 9 | HG00558.hp1 HG01256.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1403-6986delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96790003 | |||||
chr2:96790031
|
C | T | 1 | a0001c0001t0004g0121 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1403-6981C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790031 | ||||||
chr2:96790250
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1403-6762C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790250 | ||||||
chr2:96790285
|
C | T | 32 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(29): Show | 32 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1403-6727C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790285 | ||||||
chr2:96790290
|
G | A | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG02071.hp2 HG02165.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1403-6722G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790290 | ||||||
chr2:96790297
|
C | T | 12 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(9): Show | 12 | HG01261.hp2 HG01358.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1403-6715C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790297 | ||||||
chr2:96790423
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1403-6589C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790423 | ||||||
chr2:96790500
|
A | G | 2 | a0001c0001t0003g0084a0001c0001t0003g0088 | 2 | HG01256.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1403-6512A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790500 | ||||||
chr2:96790675
|
C | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0058 | 3 | HG00544.hp2 NA19000.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1403-6337C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790675 | ||||||
chr2:96790749
|
G | A | 1 | a0001c0001t0006g0234 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1403-6263G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790749 | ||||||
chr2:96790841
|
T | C | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-6171T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790841 | ||||||
chr2:96791013
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1403-5999G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791013 | ||||||
chr2:96791119
|
C | CA | 7 | a0001c0001t0001g0043a0001c0001t0001g0172a0001c0001t0001g0176others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1403-5874dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96791119 | |||||
chr2:96791119
|
CA | C | 17 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0041others(14): Show | 17 | HG00558.hp1 HG00642.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1403-5874delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96791119 | |||||
chr2:96791277
|
G | T | 9 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1403-5735G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791277 | ||||||
chr2:96791305
|
A | G | 1 | a0001c0001t0002g0156 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1403-5707A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791305 | ||||||
chr2:96791382
|
G | A | 27 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0123others(24): Show | 27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1403-5630G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791382 | ||||||
chr2:96791483
|
AT | A | 3 | a0001c0001t0005g0092a0001c0001t0006g0076a0001c0001t0006g0077 | 3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1403-5527delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96791483 | |||||
chr2:96791505
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1403-5507C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791505 | ||||||
chr2:96791550
|
C | T | 1 | a0001c0001t0004g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1403-5462C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791550 | ||||||
chr2:96791588
|
C | CA | 15 | a0001c0001t0001g0038a0001c0001t0001g0210a0001c0001t0001g0238others(12): Show | 15 | HG00639.hp1 HG02055.hp1 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.1403-5410dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96791588 | |||||
chr2:96791652
|
T | A | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-5360T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791652 | ||||||
chr2:96792019
|
C | T | 11 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0124others(8): Show | 11 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1403-4993C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792019 | ||||||
chr2:96792112
|
G | A | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-4900G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792112 | ||||||
chr2:96792208
|
T | G | 1 | a0001c0001t0007g0166 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1403-4804T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792208 | ||||||
chr2:96792245
|
C | CA | 30 | a0001c0001t0001g0040a0001c0001t0001g0046a0001c0001t0001g0058others(27): Show | 30 | HG00423.hp1 HG00642.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1403-4751dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96792245 | |||||
chr2:96792307
|
G | A | 3 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0006g0078 | 3 | HG00642.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1403-4705G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792307 | ||||||
chr2:96792416
|
C | A | 1 | a0001c0001t0001g0229 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1403-4596C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792416 | ||||||
chr2:96792448
|
G | A | 1 | a0001c0001t0003g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1403-4564G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792448 | ||||||
chr2:96792668
|
G | A | 3 | a0001c0001t0004g0123a0001c0001t0004g0128a0001c0001t0004g0129 | 3 | HG01891.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1403-4344G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792668 | ||||||
chr2:96792699
|
C | T | 156 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(153): Show | 156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1403-4313C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792699 | ||||||
chr2:96792794
|
C | A | 1 | a0001c0001t0002g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1403-4218C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792794 | ||||||
chr2:96792824
|
A | G | 68 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(65): Show | 68 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.1403-4188A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792824 | ||||||
chr2:96792855
|
G | C | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1403-4157G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792855 | ||||||
chr2:96793666
|
A | T | 33 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-3346A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96793666 | ||||||
chr2:96793793
|
G | A | 60 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(57): Show | 60 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1403-3219G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96793793 | ||||||
chr2:96793870
|
G | A | 1 | a0001c0001t0004g0117 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1403-3142G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96793870 | ||||||
chr2:96793905
|
A | G | 31 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1403-3107A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96793905 | ||||||
chr2:96794183
|
A | G | 156 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(153): Show | 156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1403-2829A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96794183 | ||||||
chr2:96794388
|
C | T | 1 | a0001c0001t0007g0166 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1403-2624C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96794388 | ||||||
chr2:96794677
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0036others(5): Show | 8 | HG00544.hp2 HG02523.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.1403-2335G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96794677 | ||||||
chr2:96794758
|
A | T | 1 | a0001c0001t0001g0177 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1403-2254A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96794758 | ||||||
chr2:96794857
|
A | G | 2 | a0001c0001t0002g0030a0001c0001t0002g0055 | 2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1403-2155A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96794857 | ||||||
chr2:96794910
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0224 | 2 | HG00609.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1403-2102G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96794910 | ||||||
chr2:96795037
|
G | A | 2 | a0001c0001t0002g0067a0001c0001t0002g0069 | 2 | HG00609.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1403-1975G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96795037 | ||||||
chr2:96795288
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1403-1724C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96795288 | ||||||
chr2:96795357
|
G | A | 1 | a0001c0002t0005g0074 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1403-1655G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96795357 | ||||||
chr2:96795487
|
A | AC | 21 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0054others(18): Show | 21 | HG00423.hp1 HG00733.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1403-1514dupC | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96795487 | |||||
chr2:96795487
|
AC | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0149others(104): Show | 108 | HG00558.hp2 HG01070.hp1 HG01070.hp2 others(105): Show |
intron_variant | MODIFIER | c.1403-1514delC | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96795487 | |||||
chr2:96795493
|
C | G | 1 | a0001c0001t0001g0267 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1403-1519C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96795493 | ||||||
chr2:96795933
|
C | T | 27 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0123others(24): Show | 27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1403-1079C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96795933 | ||||||
chr2:96796131
|
C | CT | 77 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 78 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1403-850dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | |||||
chr2:96796131
|
C | CTT | 21 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0041others(18): Show | 21 | HG01175.hp1 HG02080.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1403-851_1403-850d others(4): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | |||||
chr2:96796131
|
CT | C | 26 | a0001c0001t0001g0091a0001c0001t0001g0187a0001c0001t0001g0213others(23): Show | 26 | HG01099.hp1 HG01261.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.1403-850delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | |||||
chr2:96796131
|
CTT | C | 26 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0084others(23): Show | 26 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1403-851_1403-850d others(4): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | |||||
chr2:96796131
|
CTTT | C | 5 | a0001c0001t0003g0075a0001c0001t0003g0085a0001c0001t0003g0096others(2): Show | 5 | HG01168.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-852_1403-850d others(5): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | |||||
chr2:96796131
|
CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0001g0195a0001c0001t0004g0123a0001c0001t0004g0128others(12): Show | 15 | HG00423.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1403-861_1403-850d others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | |||||
chr2:96796131
|
CTTTTTTT others(6): Show |
C | 6 | a0001c0001t0001g0170a0001c0001t0001g0194a0001c0001t0001g0196others(3): Show | 6 | HG02965.hp2 HG04204.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.1403-862_1403-850d others(15): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | |||||
chr2:96796131
|
CTTTTTTT others(7): Show |
C | 7 | a0001c0001t0002g0014a0001c0001t0002g0028a0001c0001t0002g0056others(4): Show | 7 | NA18949.hp2 NA18951.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1403-863_1403-850d others(16): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | |||||
chr2:96796214
|
G | A | 5 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0190others(2): Show | 5 | HG01070.hp1 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-798G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96796214 | ||||||
chr2:96796269
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1403-743C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96796269 | ||||||
chr2:96796344
|
C | T | 1 | a0001c0001t0012g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1403-668C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96796344 | ||||||
chr2:96796491
|
G | A | 27 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0123others(24): Show | 27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1403-521G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96796491 | ||||||
chr2:96796633
|
C | T | 1 | a0001c0001t0006g0188 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1403-379C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96796633 | ||||||
chr2:96797291
|
C | G | 5 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546+136C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 2/6 | chr2 | 96797291 | ||||||
chr2:96797333
|
C | T | 6 | a0001c0001t0001g0169a0001c0001t0001g0197a0001c0001t0001g0198others(3): Show | 6 | HG00323.hp1 HG00733.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1546+178C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 2/6 | chr2 | 96797333 | ||||||
chr2:96797358
|
T | C | 156 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(153): Show | 156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1547-155T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 2/6 | chr2 | 96797358 | ||||||
chr2:96797441
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1547-72C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 2/6 | chr2 | 96797441 | ||||||
chr2:96797691
|
C | T | 1 | a0001c0001t0003g0109 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1681+44C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96797691 | ||||||
chr2:96797718
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1681+71G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96797718 | ||||||
chr2:96797791
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1681+144C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96797791 | ||||||
chr2:96797792
|
G | A | 154 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(151): Show | 154 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1681+145G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96797792 | ||||||
chr2:96797846
|
C | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(6): Show | 9 | HG00642.hp2 HG00741.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1681+199C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96797846 | ||||||
chr2:96797848
|
G | A | 3 | a0001c0001t0005g0092a0001c0001t0006g0076a0001c0001t0006g0077 | 3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1681+201G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96797848 | ||||||
chr2:96798095
|
G | T | 1 | a0001c0001t0003g0101 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1681+448G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96798095 | ||||||
chr2:96798320
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1681+673C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96798320 | ||||||
chr2:96798540
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG01192.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1682-517C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96798540 | ||||||
chr2:96798689
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1682-368C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96798689 | ||||||
chr2:96798831
|
A | G | 2 | a0001c0001t0003g0096a0001c0001t0003g0113 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1682-226A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96798831 | ||||||
chr2:96798909
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1682-148G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96798909 | ||||||
chr2:96799041
|
C | T | 1 | a0001c0001t0006g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1682-16C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96799041 | ||||||
chr2:96799285
|
A | G | 1 | a0001c0001t0006g0188 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1851+59A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 4/6 | chr2 | 96799285 | ||||||
chr2:96799327
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1851+101G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 4/6 | chr2 | 96799327 | ||||||
chr2:96799954
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1948+306A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96799954 | ||||||
chr2:96799988
|
C | T | 1 | a0001c0001t0003g0095 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1948+340C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96799988 | ||||||
chr2:96800097
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1948+449G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96800097 | ||||||
chr2:96800592
|
G | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0224 | 2 | HG00609.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1948+944G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96800592 | ||||||
chr2:96800873
|
GC | G | 33 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0117others(30): Show | 33 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1948+1227delC | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96800873 | |||||
chr2:96801001
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1948+1353C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801001 | ||||||
chr2:96801246
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1948+1598G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801246 | ||||||
chr2:96801507
|
G | GAGAGACC others(42): Show |
1 | a0001c0001t0001g0261 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1948+1908_1948+195 others(53): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801507 | |||||
chr2:96801509
|
G | T | 5 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0190others(2): Show | 5 | HG01070.hp1 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1948+1861G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801509 | ||||||
chr2:96801512
|
A | C | 5 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0190others(2): Show | 5 | HG01070.hp1 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1948+1864A>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801512 | ||||||
chr2:96801513
|
C | A | 5 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0190others(2): Show | 5 | HG01070.hp1 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1948+1865C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801513 | ||||||
chr2:96801527
|
A | G | 2 | a0001c0001t0002g0067a0001c0001t0002g0069 | 2 | HG00609.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1948+1879A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801527 | ||||||
chr2:96801537
|
CAG | C | 3 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006 | 3 | HG02145.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1948+1895_1948+189 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801537 | |||||
chr2:96801585
|
ACAGAGAG others(55): Show |
A | 3 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006 | 3 | HG02145.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1948+1957_1948+201 others(66): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801585 | |||||
chr2:96801596
|
ACACACAC others(6): Show |
A | 1 | a0001c0001t0005g0142 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1948+1967_1948+197 others(17): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801596 | |||||
chr2:96801600
|
ACACAGAG others(49): Show |
A | 2 | a0001c0001t0002g0002a0001c0001t0002g0003 | 2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1948+1957_1948+201 others(60): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801600 | |||||
chr2:96801656
|
C | CCA | 6 | a0001c0001t0001g0032a0001c0001t0002g0014a0001c0001t0002g0028others(3): Show | 6 | NA18949.hp2 NA18951.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.1948+2025_1948+202 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801656 | |||||
chr2:96801656
|
C | CCACACA | 3 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006 | 3 | HG02145.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1948+2021_1948+202 others(10): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801656 | |||||
chr2:96801673
|
C | G | 2 | a0001c0001t0006g0076a0001c0001t0006g0077 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1948+2025C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801673 | ||||||
chr2:96801724
|
C | CAG | 30 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(27): Show | 30 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1948+2080_1948+208 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801724 | |||||
chr2:96801729
|
A | AGACC | 36 | a0001c0001t0002g0219a0001c0001t0004g0079a0001c0001t0004g0080others(33): Show | 36 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1948+2081_1948+208 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801729 | ||||||
chr2:96801730
|
C | A | 36 | a0001c0001t0002g0219a0001c0001t0004g0079a0001c0001t0004g0080others(33): Show | 36 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1948+2082C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801730 | ||||||
chr2:96801752
|
C | A | 9 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1948+2104C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801752 | ||||||
chr2:96801780
|
C | G | 10 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0124others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1948+2132C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801780 | ||||||
chr2:96801803
|
T | G | 33 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0117others(30): Show | 33 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1948+2155T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801803 | ||||||
chr2:96801832
|
C | T | 1 | a0001c0001t0003g0101 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1948+2184C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801832 | ||||||
chr2:96801917
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1948+2269C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801917 | ||||||
chr2:96802002
|
GAC | G | 5 | a0001c0001t0006g0078a0001c0001t0006g0234a0001c0001t0006g0235others(2): Show | 5 | HG00642.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1948+2368_1948+236 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96802002 | |||||
chr2:96802173
|
C | T | 33 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0117others(30): Show | 33 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1948+2525C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96802173 | ||||||
chr2:96802445
|
C | T | 1 | a0001c0001t0008g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1948+2797C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96802445 | ||||||
chr2:96802539
|
G | C | 66 | a0001c0001t0002g0219a0001c0001t0003g0075a0001c0001t0003g0081others(63): Show | 66 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(63): Show |
intron_variant | MODIFIER | c.1948+2891G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96802539 | ||||||
chr2:96803012
|
G | T | 1 | a0001c0001t0003g0105 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1948+3364G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803012 | ||||||
chr2:96803339
|
T | G | 1 | a0001c0001t0003g0088 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1948+3691T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803339 | ||||||
chr2:96803453
|
G | A | 1 | a0001c0001t0002g0073 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1948+3805G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803453 | ||||||
chr2:96803641
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0002g0219 | 2 | HG03453.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1948+3993G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803641 | ||||||
chr2:96803725
|
TA | T | 116 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0002g0002others(113): Show | 116 | HG00609.hp1 HG00642.hp1 HG01070.hp2 others(113): Show |
intron_variant | MODIFIER | c.1948+4090delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96803725 | |||||
chr2:96803739
|
C | G | 2 | a0001c0001t0002g0030a0001c0001t0002g0055 | 2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1948+4091C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803739 | ||||||
chr2:96803881
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1948+4233T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803881 | ||||||
chr2:96803897
|
T | C | 10 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0124others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1948+4249T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803897 | ||||||
chr2:96804074
|
T | A | 1 | a0001c0001t0005g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1948+4426T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96804074 | ||||||
chr2:96804226
|
A | AT | 5 | a0001c0001t0001g0171a0001c0001t0001g0202a0001c0001t0001g0218others(2): Show | 5 | HG00639.hp2 HG02886.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1949-4314dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96804226 | |||||
chr2:96804226
|
AT | A | 18 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0160others(15): Show | 18 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1949-4314delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96804226 | |||||
chr2:96804486
|
C | T | 32 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0082others(29): Show | 32 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1949-4075C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96804486 | ||||||
chr2:96804561
|
T | C | 1 | a0001c0001t0003g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1949-4000T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96804561 | ||||||
chr2:96804637
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0183 | 2 | NA18943.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1949-3924G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96804637 | ||||||
chr2:96804778
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0191 | 2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1949-3783C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96804778 | ||||||
chr2:96804782
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1949-3779C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96804782 | ||||||
chr2:96805170
|
G | A | 33 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0117others(30): Show | 33 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1949-3391G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805170 | ||||||
chr2:96805284
|
ACTATAAA others(32): Show |
A | 1 | a0001c0001t0005g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1949-3273_1949-323 others(43): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96805284 | |||||
chr2:96805418
|
G | GT | 76 | a0001c0001t0001g0021a0001c0001t0001g0066a0001c0001t0001g0071others(73): Show | 76 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1949-3122dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96805418 | |||||
chr2:96805418
|
G | GTT | 41 | a0001c0001t0001g0196a0001c0001t0001g0205a0001c0001t0002g0002others(38): Show | 41 | HG00609.hp1 HG00642.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.1949-3123_1949-312 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96805418 | |||||
chr2:96805418
|
G | GTTT | 28 | a0001c0001t0002g0057a0001c0001t0002g0152a0001c0001t0003g0075others(25): Show | 28 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1949-3124_1949-312 others(7): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96805418 | |||||
chr2:96805418
|
GT | G | 10 | a0001c0001t0001g0044a0001c0001t0001g0182a0001c0001t0001g0252others(7): Show | 10 | HG00280.hp2 HG01517.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1949-3122delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96805418 | |||||
chr2:96805426
|
T | A | 3 | a0001c0001t0007g0167a0001c0001t0007g0168a0001c0009t0007g0193 | 3 | HG02145.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1949-3135T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805426 | ||||||
chr2:96805432
|
T | A | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1949-3129T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805432 | ||||||
chr2:96805433
|
T | A | 3 | a0001c0001t0007g0167a0001c0001t0007g0168a0001c0009t0007g0193 | 3 | HG02145.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1949-3128T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805433 | ||||||
chr2:96805437
|
T | A | 15 | a0001c0001t0004g0123a0001c0001t0004g0151a0001c0001t0005g0092others(12): Show | 15 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1949-3124T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805437 | ||||||
chr2:96805437
|
T | TA | 7 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1949-3124_1949-312 others(5): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805437 | ||||||
chr2:96805438
|
T | A | 1 | a0001c0001t0001g0025 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1949-3123T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805438 | ||||||
chr2:96805439
|
TA | T | 9 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0035others(6): Show | 9 | HG00323.hp2 HG00558.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1949-3121delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805439 | ||||||
chr2:96805440
|
A | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(47): Show | 51 | HG00280.hp1 HG00639.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.1949-3121A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805440 | ||||||
chr2:96805443
|
A | T | 3 | a0001c0001t0001g0066a0001c0001t0007g0166a0001c0001t0012g0116 | 3 | HG02055.hp1 HG02056.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1949-3118A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805443 | ||||||
chr2:96805445
|
T | A | 1 | a0001c0001t0012g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1949-3116T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805445 | ||||||
chr2:96805445
|
T | TA | 29 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0117others(26): Show | 29 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.1949-3116_1949-311 others(5): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805445 | ||||||
chr2:96805454
|
A | C | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1949-3107A>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805454 | ||||||
chr2:96805500
|
T | G | 1 | a0001c0001t0005g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1949-3061T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805500 | ||||||
chr2:96805637
|
T | G | 2 | a0001c0001t0004g0079a0001c0001t0004g0080 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1949-2924T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805637 | ||||||
chr2:96805644
|
T | A | 1 | a0001c0001t0002g0237 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1949-2917T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805644 | ||||||
chr2:96805657
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1949-2904G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805657 | ||||||
chr2:96806025
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1949-2536C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806025 | ||||||
chr2:96806043
|
ACCTCCCG others(94): Show |
A | 10 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0124others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1949-2490_1949-239 others(4): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806043 | |||||
chr2:96806053
|
C | A | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1949-2508C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806053 | ||||||
chr2:96806080
|
G | A | 13 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0003g0097others(10): Show | 13 | HG01981.hp2 HG02155.hp2 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.1949-2481G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806080 | ||||||
chr2:96806081
|
A | AC | 22 | a0001c0001t0002g0159a0001c0001t0004g0117a0001c0001t0004g0118others(19): Show | 22 | HG01261.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1949-2472dupC | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806081 | |||||
chr2:96806090
|
A | C | 23 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119others(20): Show | 23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1949-2471A>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806090 | ||||||
chr2:96806105
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1949-2456G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806105 | ||||||
chr2:96806105
|
GGGGGCGG others(42): Show |
G | 1 | a0001c0001t0001g0201 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1949-2427_1949-237 others(53): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806105 | |||||
chr2:96806126
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1949-2435G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806126 | ||||||
chr2:96806143
|
G | T | 23 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119others(20): Show | 23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1949-2418G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806143 | ||||||
chr2:96806154
|
C | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0229a0001c0001t0001g0231 | 3 | HG01361.hp1 HG01934.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1949-2407C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806154 | ||||||
chr2:96806317
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1949-2244A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806317 | ||||||
chr2:96806426
|
C | T | 80 | a0001c0001t0001g0021a0001c0001t0001g0090a0001c0001t0001g0091others(77): Show | 80 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1949-2135C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806426 | ||||||
chr2:96806506
|
A | AAC | 26 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0025others(23): Show | 26 | HG00609.hp1 HG00673.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1949-2026_1949-202 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | |||||
chr2:96806506
|
A | AACAC | 23 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0041others(20): Show | 23 | HG00558.hp1 HG01884.hp2 HG02080.hp1 others(20): Show |
intron_variant | MODIFIER | c.1949-2028_1949-202 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | |||||
chr2:96806506
|
A | AACACAC | 5 | a0001c0001t0002g0002a0001c0001t0004g0128a0001c0001t0004g0129others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1949-2030_1949-202 others(10): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | |||||
chr2:96806506
|
A | AACACACA others(3): Show |
1 | a0001c0001t0002g0155 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1949-2034_1949-202 others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | |||||
chr2:96806506
|
A | AACACACA others(7): Show |
1 | a0001c0001t0002g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1949-2038_1949-202 others(18): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | |||||
chr2:96806506
|
A | AACACACA others(9): Show |
2 | a0001c0001t0002g0145a0001c0001t0002g0158 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1949-2040_1949-202 others(20): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | |||||
chr2:96806506
|
AAC | A | 8 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0175others(5): Show | 8 | HG01168.hp2 HG02109.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.1949-2026_1949-202 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | |||||
chr2:96806506
|
AACAC | A | 3 | a0001c0001t0006g0076a0001c0001t0006g0077a0001c0001t0008g0239 | 3 | HG01891.hp2 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1949-2028_1949-202 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | |||||
chr2:96806528
|
C | A | 1 | a0001c0001t0012g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1949-2033C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806528 | ||||||
chr2:96806529
|
ACACACAC others(5): Show |
A | 1 | a0001c0001t0008g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1949-2030_1949-201 others(16): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806529 | |||||
chr2:96806529
|
ACACACAC others(13): Show |
A | 1 | a0001c0001t0001g0208 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1949-2030_1949-201 others(24): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806529 | |||||
chr2:96806531
|
A | ACG | 3 | a0001c0001t0001g0211a0001c0001t0001g0214a0001c0001t0001g0253 | 3 | HG00280.hp2 HG00423.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1949-2029_1949-202 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806531 | |||||
chr2:96806531
|
A | G | 1 | a0001c0001t0008g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1949-2030A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806531 | ||||||
chr2:96806533
|
A | ACG | 12 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0161others(9): Show | 12 | HG00544.hp2 HG00639.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.1949-2027_1949-202 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806533 | |||||
chr2:96806533
|
A | G | 9 | a0001c0001t0001g0184a0001c0001t0001g0211a0001c0001t0001g0214others(6): Show | 9 | HG00099.hp2 HG00423.hp1 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.1949-2028A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806533 | ||||||
chr2:96806533
|
ACACG | A | 6 | a0001c0001t0006g0078a0001c0001t0006g0188a0001c0001t0006g0234others(3): Show | 6 | HG00642.hp1 HG02572.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1949-2026_1949-202 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806533 | |||||
chr2:96806535
|
A | ACACACAC others(13): Show |
1 | a0001c0001t0002g0152 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1949-2025_1949-202 others(24): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
A | ACACACAC others(9): Show |
3 | a0001c0001t0002g0147a0001c0001t0002g0154a0001c0001t0002g0159 | 3 | HG01261.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(20): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
A | ACACACAC others(11): Show |
1 | a0001c0001t0002g0146 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1949-2025_1949-202 others(22): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
A | ACACACAC others(7): Show |
2 | a0001c0001t0002g0153a0001c0001t0002g0156 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(18): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
A | ACACACG | 7 | a0001c0001t0001g0012a0001c0001t0002g0003a0001c0001t0003g0075others(4): Show | 7 | HG01256.hp2 HG01993.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(10): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
A | ACACACGC others(1): Show |
5 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0099others(2): Show | 5 | HG01099.hp1 HG01261.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(12): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
A | ACACACGC others(5): Show |
1 | a0001c0001t0003g0100 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1949-2025_1949-202 others(16): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
A | ACACG | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0016others(12): Show | 15 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
A | ACACGCG | 8 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0197others(5): Show | 8 | HG00642.hp2 HG01169.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(10): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
A | ACACGCGC others(1): Show |
3 | a0001c0001t0003g0097a0001c0001t0003g0107a0001c0001t0013g0108 | 3 | NA19054.hp1 NA19064.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(12): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
A | ACACGCGC others(3): Show |
1 | a0001c0001t0003g0109 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1949-2025_1949-202 others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
A | ACACGCGC others(5): Show |
1 | a0001c0001t0003g0114 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1949-2025_1949-202 others(16): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
A | ACG | 22 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0024others(19): Show | 22 | HG00544.hp1 HG01255.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1949-2008_1949-200 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
A | G | 31 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0043others(28): Show | 31 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1949-2026A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806535 | ||||||
chr2:96806535
|
ACG | A | 4 | a0001c0001t0002g0028a0001c0001t0002g0057a0001c0001t0002g0062others(1): Show | 4 | HG02717.hp2 HG06807.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1949-2008_1949-200 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806535
|
ACGCGCGC others(3): Show |
A | 1 | a0001c0001t0007g0166 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1949-2016_1949-200 others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | |||||
chr2:96806537
|
G | A | 47 | a0001c0001t0001g0052a0001c0001t0001g0205a0001c0001t0002g0004others(44): Show | 47 | HG00609.hp1 HG00673.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.1949-2024G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806537 | ||||||
chr2:96806539
|
G | A | 24 | a0001c0001t0002g0062a0001c0001t0002g0115a0001c0001t0002g0155others(21): Show | 24 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1949-2022G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806539 | ||||||
chr2:96806541
|
G | A | 2 | a0001c0001t0002g0062a0001c0001t0002g0115 | 2 | HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1949-2020G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806541 | ||||||
chr2:96806546
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0015g0242 | 2 | HG00099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1949-2015C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806546 | ||||||
chr2:96806873
|
C | G | 1 | a0001c0001t0012g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1949-1688C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806873 | ||||||
chr2:96806993
|
T | A | 1 | a0001c0001t0006g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1949-1568T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806993 | ||||||
chr2:96807068
|
T | C | 6 | a0001c0001t0004g0117a0001c0001t0004g0118a0001c0001t0004g0119others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1949-1493T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807068 | ||||||
chr2:96807096
|
C | T | 1 | a0001c0001t0004g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1949-1465C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807096 | ||||||
chr2:96807261
|
G | A | 11 | a0001c0001t0005g0126a0001c0001t0005g0143a0001c0002t0005g0074others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1949-1300G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807261 | ||||||
chr2:96807286
|
G | A | 10 | a0001c0001t0004g0079a0001c0001t0004g0080a0001c0001t0004g0124others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1949-1275G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807286 | ||||||
chr2:96807381
|
G | T | 1 | a0001c0001t0001g0204 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1949-1180G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807381 | ||||||
chr2:96807559
|
C | A | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1949-1002C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807559 | ||||||
chr2:96807751
|
C | T | 1 | a0001c0001t0008g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1949-810C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807751 | ||||||
chr2:96807752
|
G | A | 8 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0130others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1949-809G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807752 | ||||||
chr2:96807872
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1949-689A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807872 | ||||||
chr2:96808029
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1949-532C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96808029 | ||||||
chr2:96808074
|
A | C | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1949-487A>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96808074 | ||||||
chr2:96808192
|
A | G | 114 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(111): Show | 114 | HG00609.hp1 HG00642.hp1 HG01070.hp2 others(111): Show |
intron_variant | MODIFIER | c.1949-369A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96808192 | ||||||
chr2:96808789
|
G | C | 1 | a0001c0002t0005g0137 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2130+47G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96808789 | ||||||
chr2:96808840
|
G | A | 1 | a0001c0001t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2130+98G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96808840 | ||||||
chr2:96809002
|
G | GT | 35 | a0001c0001t0001g0060a0001c0001t0002g0057a0001c0001t0002g0067others(32): Show | 35 | HG01884.hp1 HG01884.hp2 HG01981.hp2 others(32): Show |
intron_variant | MODIFIER | c.2130+274dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 96809002 | |||||
chr2:96809088
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2131-232C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96809088 | ||||||
chr2:96809102
|
G | C | 1 | a0001c0001t0001g0023 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2131-218G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96809102 | ||||||
chr2:96809143
|
T | A | 8 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0130others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2131-177T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96809143 | ||||||
chr2:96809150
|
C | T | 1 | a0001c0001t0003g0113 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2131-170C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96809150 | ||||||
chr2:96809165
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2131-155C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96809165 | ||||||
chr2:96809199
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2131-121C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96809199 |