geneid | 79585 |
---|---|
ensemblid | ENSG00000262246.6 |
hgncid | 26161 |
symbol | CORO7 |
name | coronin 7 |
refseq_nuc | NM_024535.5 |
refseq_prot | NP_078811.3 |
ensembl_nuc | ENST00000251166.9 |
ensembl_prot | ENSP00000251166.4 |
mane_status | MANE Select |
chr | chr16 |
start | 4354542 |
end | 4416596 |
strand | - |
ver | v1.2 |
region | chr16:4354542-4416596 |
region5000 | chr16:4349542-4421596 |
regionname0 | CORO7_chr16_4354542_4416596 |
regionname5000 | CORO7_chr16_4349542_4421596 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 925 | 133 | 53 | 26 | 34 | 5 | 14 | 23 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0002 | 0/0 | 925 | 127 | 14 | 32 | 54 | 7 | 20 | 37 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0003 | 0/0 | 925 | 17 | 17 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0004 | 0/0 | 925 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0005 | 0/0 | 925 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0006 | 0/0 | 925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0007 | 0/0 | 925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0008 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0009 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0010 | 0/0 | 925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0011 | 0/0 | 925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0012 | 0/0 | 925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0013 | 0/0 | 925 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0014 | 0/0 | 925 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0015 | 0/0 | 925 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0016 | 0/0 | 925 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0017 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0018 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0019 | 0/0 | 925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2778 | 123 | 14 | 29 | 53 | 7 | 20 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0002 | 0/1 | 2778 | 118 | 38 | 26 | 34 | 5 | 14 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0003 | 0/0 | 2778 | 15 | 15 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0004 | 0/0 | 2778 | 13 | 13 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0005 | 0/0 | 2778 | 4 | 4 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0006 | 0/0 | 2778 | 3 | 0 | 3 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0007 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0008 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0009 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0010 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0011 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0012 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0013 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0014 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0015 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0016 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0017 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0018 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0019 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0020 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0021 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0022 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0023 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0024 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0025 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
c0026 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 695 | 244 | 70 | 55 | 74 | 10 | 34 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
t0002 | 0/0 | 695 | 50 | 22 | 6 | 16 | 2 | 4 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
t0003 | 0/0 | 695 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
t0004 | 0/0 | 695 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
t0005 | 0/0 | 695 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0025 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/1 | 2778 | 118 | 38 | 26 | 34 | 5 | 14 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0001c0004 | 0/0 | 2778 | 13 | 13 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0001c0014 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0001c0023 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0002c0001 | 0/0 | 2778 | 123 | 14 | 29 | 53 | 7 | 20 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0002c0006 | 0/0 | 2778 | 3 | 0 | 3 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0002c0013 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0003c0003 | 0/0 | 2778 | 15 | 15 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0003c0018 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0003c0019 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0004c0005 | 0/0 | 2778 | 4 | 4 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0005c0007 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0006c0026 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0007c0025 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0008c0024 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0009c0008 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0010c0012 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0011c0011 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0012c0010 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0013c0009 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0014c0017 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0015c0021 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0016c0022 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0017c0020 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0018c0016 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0019c0015 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/1 | 3472 | 72 | 19 | 20 | 19 | 3 | 10 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0001c0002t0002 | 0/0 | 3472 | 46 | 19 | 6 | 15 | 2 | 4 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0001c0004t0001 | 0/0 | 3472 | 13 | 13 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0001c0014t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0001c0023t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0002c0001t0001 | 0/0 | 3472 | 121 | 14 | 28 | 52 | 7 | 20 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0002c0001t0002 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0002c0001t0004 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0002c0006t0001 | 0/0 | 3472 | 3 | 0 | 3 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0002c0013t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0003c0003t0001 | 0/0 | 3472 | 15 | 15 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0003c0018t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0003c0019t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0004c0005t0001 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0004c0005t0002 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0005c0007t0001 | 0/0 | 3472 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0006c0026t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0007c0025t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0008c0024t0005 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0009c0008t0002 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0010c0012t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0011c0011t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0012c0010t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0013c0009t0001 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0014c0017t0001 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0015c0021t0001 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0016c0022t0001 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0017c0020t0002 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0018c0016t0003 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
a0019c0015t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | copy fasta | chr16 | 4349542 | 4421596 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0025 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0002t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0004t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0004t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0014t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0001c0023t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0006t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0006t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0002c0013t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0018t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0003c0019t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0004c0005t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0004c0005t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0004c0005t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0004c0005t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0005c0007t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0005c0007t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0006c0026t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0007c0025t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0008c0024t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0009c0008t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0010c0012t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0011c0011t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0012c0010t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0013c0009t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0014c0017t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0015c0021t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0016c0022t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0017c0020t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0018c0016t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
a0019c0015t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0087 | EUR | GBR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00099 | hp2 | a0002 | c0001 | t0001 | g0176 | EUR | GBR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00140 | hp1 | a0002 | c0001 | t0001 | g0045 | EUR | GBR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0104 | EUR | GBR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00280 | hp1 | a0002 | c0001 | t0001 | g0010 | EUR | FIN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00280 | hp2 | a0002 | c0001 | t0001 | g0226 | EUR | FIN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00423 | hp2 | a0002 | c0001 | t0001 | g0214 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00544 | hp2 | a0002 | c0001 | t0001 | g0249 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00597 | hp1 | a0002 | c0001 | t0001 | g0195 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00639 | hp1 | a0002 | c0001 | t0001 | g0175 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00639 | hp2 | a0002 | c0001 | t0001 | g0194 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00642 | hp2 | a0002 | c0001 | t0001 | g0202 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00673 | hp2 | a0002 | c0001 | t0001 | g0180 | EAS | CHS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00733 | hp1 | a0013 | c0009 | t0001 | g0247 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00738 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00741 | hp1 | a0002 | c0001 | t0001 | g0187 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01069 | hp2 | a0002 | c0001 | t0001 | g0182 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01070 | hp2 | a0002 | c0001 | t0001 | g0213 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01081 | hp1 | a0002 | c0001 | t0001 | g0211 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01099 | hp1 | a0015 | c0021 | t0001 | g0032 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01099 | hp2 | a0016 | c0022 | t0001 | g0123 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01106 | hp1 | a0002 | c0006 | t0001 | g0248 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01106 | hp2 | a0002 | c0001 | t0001 | g0165 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01109 | hp1 | a0002 | c0001 | t0001 | g0205 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01168 | hp1 | a0002 | c0001 | t0001 | g0011 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01168 | hp2 | a0002 | c0001 | t0001 | g0164 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01243 | hp1 | a0002 | c0001 | t0001 | g0168 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | PUR | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01255 | hp1 | a0002 | c0001 | t0001 | g0033 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01257 | hp1 | a0002 | c0001 | t0001 | g0166 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01257 | hp2 | a0002 | c0006 | t0001 | g0013 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01258 | hp1 | a0002 | c0006 | t0001 | g0013 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01258 | hp2 | a0002 | c0001 | t0001 | g0204 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01261 | hp1 | a0002 | c0001 | t0004 | g0192 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01346 | hp1 | a0002 | c0001 | t0001 | g0156 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01361 | hp1 | a0002 | c0001 | t0001 | g0155 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01496 | hp1 | a0014 | c0017 | t0001 | g0077 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01496 | hp2 | a0002 | c0001 | t0001 | g0179 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0076 | EUR | IBS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0092 | EUR | IBS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01516 | hp1 | a0002 | c0001 | t0001 | g0167 | EUR | IBS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0070 | EUR | IBS | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01884 | hp1 | a0002 | c0001 | t0001 | g0252 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0137 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01928 | hp1 | a0002 | c0001 | t0001 | g0209 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0118 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01934 | hp1 | a0002 | c0001 | t0001 | g0160 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0055 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01943 | hp1 | a0002 | c0001 | t0001 | g0208 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0075 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01952 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0117 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01975 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02015 | hp1 | a0002 | c0001 | t0001 | g0235 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02015 | hp2 | a0002 | c0001 | t0001 | g0200 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02027 | hp2 | a0002 | c0001 | t0001 | g0016 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02040 | hp1 | a0002 | c0001 | t0001 | g0221 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02040 | hp2 | a0002 | c0001 | t0001 | g0061 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0089 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02055 | hp2 | a0002 | c0001 | t0001 | g0119 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0227 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02056 | hp2 | a0002 | c0001 | t0001 | g0234 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02071 | hp1 | a0002 | c0001 | t0001 | g0222 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02080 | hp1 | a0002 | c0001 | t0001 | g0236 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02080 | hp2 | a0002 | c0001 | t0001 | g0154 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02083 | hp2 | a0002 | c0001 | t0001 | g0199 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02145 | hp1 | a0002 | c0001 | t0001 | g0210 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02145 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02148 | hp1 | a0002 | c0001 | t0001 | g0095 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02148 | hp2 | a0002 | c0001 | t0001 | g0188 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | CDX | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02155 | hp2 | a0002 | c0001 | t0001 | g0223 | EAS | CDX | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02258 | hp1 | a0002 | c0001 | t0001 | g0120 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02273 | hp2 | a0002 | c0001 | t0001 | g0190 | AMR | PEL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02280 | hp1 | a0003 | c0003 | t0001 | g0262 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02280 | hp2 | a0001 | c0004 | t0001 | g0136 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02451 | hp1 | a0003 | c0003 | t0001 | g0014 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0267 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | KHV | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0245 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02602 | hp1 | a0002 | c0001 | t0001 | g0171 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02602 | hp2 | a0010 | c0012 | t0001 | g0197 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02615 | hp1 | a0003 | c0003 | t0001 | g0265 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02622 | hp1 | a0002 | c0001 | t0001 | g0132 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02622 | hp2 | a0001 | c0004 | t0001 | g0244 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0122 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02698 | hp1 | a0002 | c0001 | t0001 | g0163 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02698 | hp2 | a0002 | c0001 | t0001 | g0186 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02723 | hp1 | a0002 | c0001 | t0001 | g0206 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02723 | hp2 | a0001 | c0014 | t0001 | g0026 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02735 | hp1 | a0002 | c0001 | t0001 | g0193 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0096 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02738 | hp1 | a0002 | c0001 | t0001 | g0170 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02738 | hp2 | a0011 | c0011 | t0001 | g0225 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02809 | hp1 | a0003 | c0003 | t0001 | g0274 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02809 | hp2 | a0002 | c0001 | t0001 | g0036 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0246 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02818 | hp2 | a0002 | c0001 | t0001 | g0144 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02886 | hp2 | a0003 | c0003 | t0001 | g0014 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02895 | hp1 | a0002 | c0001 | t0001 | g0141 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02895 | hp2 | a0004 | c0005 | t0001 | g0258 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02896 | hp1 | a0002 | c0001 | t0001 | g0149 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02896 | hp2 | a0003 | c0003 | t0001 | g0276 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02897 | hp1 | a0004 | c0005 | t0001 | g0256 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02897 | hp2 | a0003 | c0018 | t0001 | g0277 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02922 | hp1 | a0008 | c0024 | t0005 | g0279 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02922 | hp2 | a0001 | c0023 | t0001 | g0040 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0150 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0041 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02970 | hp1 | a0003 | c0003 | t0001 | g0264 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02970 | hp2 | a0002 | c0001 | t0001 | g0212 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0161 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02976 | hp2 | a0003 | c0003 | t0001 | g0273 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03017 | hp2 | a0002 | c0001 | t0001 | g0232 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03041 | hp1 | a0005 | c0007 | t0001 | g0042 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03041 | hp2 | a0003 | c0003 | t0001 | g0266 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03098 | hp1 | a0003 | c0003 | t0001 | g0263 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03130 | hp2 | a0004 | c0005 | t0002 | g0260 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03139 | hp2 | a0004 | c0005 | t0001 | g0257 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0056 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03209 | hp1 | a0003 | c0003 | t0001 | g0268 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0094 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03239 | hp2 | a0002 | c0001 | t0001 | g0162 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03453 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03486 | hp1 | a0005 | c0007 | t0001 | g0043 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0121 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03490 | hp1 | a0002 | c0001 | t0001 | g0142 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0106 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03491 | hp2 | a0002 | c0001 | t0001 | g0189 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03516 | hp2 | a0003 | c0019 | t0001 | g0272 | AFR | ESN | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03540 | hp1 | a0003 | c0003 | t0001 | g0270 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0085 | AFR | GWD | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0152 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03654 | hp2 | a0002 | c0001 | t0001 | g0110 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03688 | hp1 | a0002 | c0001 | t0001 | g0012 | SAS | STU | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0126 | SAS | STU | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03704 | hp1 | a0002 | c0001 | t0001 | g0012 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03704 | hp2 | a0002 | c0001 | t0001 | g0253 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03710 | hp1 | a0002 | c0001 | t0001 | g0158 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0084 | SAS | PJL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03834 | hp1 | a0019 | c0015 | t0001 | g0124 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03834 | hp2 | a0002 | c0001 | t0001 | g0230 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03927 | hp1 | a0002 | c0001 | t0001 | g0159 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03942 | hp1 | a0002 | c0001 | t0001 | g0233 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0250 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG04184 | hp1 | a0002 | c0001 | t0001 | g0172 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG04184 | hp2 | a0007 | c0025 | t0001 | g0243 | SAS | BEB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0029 | SAS | STU | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG04199 | hp2 | a0002 | c0001 | t0001 | g0174 | SAS | STU | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0083 | SAS | STU | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0169 | SAS | STU | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18522 | hp1 | a0002 | c0001 | t0001 | g0183 | AFR | YRI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18522 | hp2 | a0003 | c0003 | t0001 | g0269 | AFR | YRI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18612 | hp1 | a0002 | c0001 | t0001 | g0191 | EAS | CHB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | CHB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18906 | hp1 | a0001 | c0004 | t0001 | g0133 | AFR | YRI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0116 | AFR | YRI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18939 | hp1 | a0012 | c0010 | t0001 | g0181 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18939 | hp2 | a0002 | c0001 | t0001 | g0219 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18942 | hp2 | a0002 | c0001 | t0001 | g0239 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18943 | hp1 | a0006 | c0026 | t0001 | g0129 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18943 | hp2 | a0002 | c0001 | t0002 | g0278 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18944 | hp1 | a0002 | c0001 | t0001 | g0224 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18946 | hp2 | a0002 | c0001 | t0001 | g0063 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18948 | hp2 | a0002 | c0001 | t0001 | g0177 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18960 | hp1 | a0002 | c0001 | t0001 | g0242 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18960 | hp2 | a0002 | c0001 | t0001 | g0143 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18962 | hp2 | a0002 | c0013 | t0001 | g0207 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18966 | hp1 | a0002 | c0001 | t0001 | g0218 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0064 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18969 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18969 | hp2 | a0002 | c0001 | t0001 | g0184 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18977 | hp2 | a0002 | c0001 | t0001 | g0185 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18978 | hp1 | a0002 | c0001 | t0001 | g0229 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18979 | hp1 | a0002 | c0001 | t0001 | g0217 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18980 | hp2 | a0002 | c0001 | t0001 | g0240 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18981 | hp1 | a0002 | c0001 | t0001 | g0196 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18982 | hp1 | a0002 | c0001 | t0001 | g0255 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18997 | hp2 | a0002 | c0001 | t0001 | g0173 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA18998 | hp2 | a0002 | c0001 | t0001 | g0140 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19000 | hp1 | a0002 | c0001 | t0001 | g0237 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19000 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19007 | hp1 | a0002 | c0001 | t0001 | g0215 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19007 | hp2 | a0002 | c0001 | t0001 | g0228 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19010 | hp2 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19030 | hp1 | a0009 | c0008 | t0002 | g0059 | AFR | LWK | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | LWK | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19043 | hp1 | a0001 | c0004 | t0001 | g0001 | AFR | LWK | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19043 | hp2 | a0003 | c0003 | t0001 | g0261 | AFR | LWK | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19054 | hp2 | a0002 | c0001 | t0001 | g0241 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19055 | hp1 | a0002 | c0001 | t0001 | g0178 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19066 | hp2 | a0002 | c0001 | t0001 | g0238 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19068 | hp1 | a0002 | c0001 | t0001 | g0069 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19068 | hp2 | a0002 | c0001 | t0001 | g0254 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19079 | hp1 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19080 | hp2 | a0002 | c0001 | t0001 | g0157 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19084 | hp2 | a0002 | c0001 | t0001 | g0128 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19087 | hp1 | a0002 | c0001 | t0001 | g0216 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19088 | hp1 | a0002 | c0001 | t0001 | g0015 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19089 | hp1 | a0002 | c0001 | t0001 | g0220 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19089 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | YRI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | YRI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | ASW | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA20129 | hp2 | a0018 | c0016 | t0003 | g0259 | AFR | ASW | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0020 | EUR | TSI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA20805 | hp2 | a0002 | c0001 | t0001 | g0071 | EUR | TSI | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA20905 | hp1 | a0002 | c0001 | t0001 | g0010 | SAS | GIH | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0060 | SAS | GIH | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG01123 | hp2 | a0002 | c0001 | t0001 | g0198 | AMR | CLM | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0148 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02486 | hp1 | a0001 | c0004 | t0001 | g0001 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02486 | hp2 | a0001 | c0004 | t0001 | g0134 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0074 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG02559 | hp2 | a0003 | c0003 | t0001 | g0271 | AFR | ACB | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0275 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG03471 | hp2 | a0001 | c0004 | t0001 | g0001 | AFR | MSL | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0135 | AFR | USA | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
HG06807 | hp2 | a0002 | c0001 | t0001 | g0139 | AFR | USA | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | USA | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA20300 | hp2 | a0002 | c0001 | t0001 | g0011 | AFR | USA | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA21309 | hp1 | a0017 | c0020 | t0002 | g0046 | AFR | LWK | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0091 | AFR | LWK | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0025 | REF | REF | CORO7_chr16_4349542_4421596 | CORO7 | chr16 | 4349542 | 4421596 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:4355303
|
C | G | 1 | a0011 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.2755G>C | p.Val919Leu | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 27/28 | 2833/3472 | 2755/2778 | 919/925 | chr16 | 4355303 | ||
chr16:4355347
|
A | G | 1 | a0012 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.2711T>C | p.Leu904Pro | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 27/28 | 2789/3472 | 2711/2778 | 904/925 | chr16 | 4355347 | ||
chr16:4357176
|
T | C | 1 | a0010 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.2677A>G | p.Lys893Glu | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/28 | 2755/3472 | 2677/2778 | 893/925 | chr16 | 4357176 | ||
chr16:4358001
|
G | A | 1 | a0015 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.2560C>T | p.Leu854Phe | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/28 | 2638/3472 | 2560/2778 | 854/925 | chr16 | 4358001 | ||
chr16:4359512
|
G | A | 1 | a0018 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.2218C>T | p.Pro740Ser | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 22/28 | 2296/3472 | 2218/2778 | 740/925 | chr16 | 4359512 | ||
chr16:4360314
|
C | T | 1 | a0016 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.2072G>A | p.Cys691Tyr | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/28 | 2150/3472 | 2072/2778 | 691/925 | chr16 | 4360314 | ||
chr16:4360356
|
G | C | 1 | a0005 | 2 | HG03041.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.2030C>G | p.Pro677Arg | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/28 | 2108/3472 | 2030/2778 | 677/925 | chr16 | 4360356 | ||
chr16:4360975
|
C | G | 1 | a0013 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.1885G>C | p.Asp629His | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/28 | 1963/3472 | 1885/2778 | 629/925 | chr16 | 4360975 | ||
chr16:4361382
|
C | T | 1 | a0017 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1666G>A | p.Asp556Asn | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 17/28 | 1744/3472 | 1666/2778 | 556/925 | chr16 | 4361382 | ||
chr16:4364344
|
C | T | 2 | a0003a0018 | 18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
missense_variant | MODERATE | c.1207G>A | p.Ala403Thr | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/28 | 1285/3472 | 1207/2778 | 403/925 | chr16 | 4364344 | ||
chr16:4364887
|
C | T | 1 | a0014 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.932G>A | p.Gly311Glu | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 12/28 | 1010/3472 | 932/2778 | 311/925 | chr16 | 4364887 | ||
chr16:4388001
|
A | G | 2 | a0004a0018 | 5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
missense_variant | MODERATE | c.770T>C | p.Leu257Ser | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/28 | 848/3472 | 770/2778 | 257/925 | chr16 | 4388001 | ||
chr16:4388056
|
C | T | 1 | a0019 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.715G>A | p.Glu239Lys | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/28 | 793/3472 | 715/2778 | 239/925 | chr16 | 4388056 | ||
chr16:4395326
|
C | T | 5 | a0002a0010a0011others(2): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
missense_variant | MODERATE | c.578G>A | p.Arg193Gln | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/28 | 656/3472 | 578/2778 | 193/925 | chr16 | 4395326 | ||
chr16:4405522
|
C | T | 1 | a0009 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.533G>A | p.Arg178Gln | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/28 | 611/3472 | 533/2778 | 178/925 | chr16 | 4405522 | ||
chr16:4405534
|
G | A | 1 | a0008 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.521C>T | p.Ala174Val | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/28 | 599/3472 | 521/2778 | 174/925 | chr16 | 4405534 | ||
chr16:4405552
|
C | G | 1 | a0008 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.503G>C | p.Gly168Ala | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/28 | 581/3472 | 503/2778 | 168/925 | chr16 | 4405552 | ||
chr16:4408182
|
G | A | 1 | a0007 | 1 | HG04184.hp2 | missense_variant&splice_region_variant | MODERATE | c.302C>T | p.Thr101Met | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/28 | 380/3472 | 302/2778 | 101/925 | chr16 | 4408182 | ||
chr16:4413314
|
G | A | 1 | a0006 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.151C>T | p.Arg51Cys | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/28 | 229/3472 | 151/2778 | 51/925 | chr16 | 4413314 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:4357186
|
G | A | 1 | a0002c0013 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.2667C>T | p.Asp889Asp | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/28 | 2745/3472 | 2667/2778 | 889/925 | chr16 | 4357186 | ||
chr16:4361223
|
C | T | 2 | a0001c0004a0015c0021 | 14 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
synonymous_variant | LOW | c.1713G>A | p.Leu571Leu | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 18/28 | 1791/3472 | 1713/2778 | 571/925 | chr16 | 4361223 | ||
chr16:4362006
|
C | T | 2 | a0002c0006a0013c0009 | 4 | HG00733.hp1 HG01106.hp1 HG01257.hp2 others(1): Show |
synonymous_variant | LOW | c.1557G>A | p.Gly519Gly | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/28 | 1635/3472 | 1557/2778 | 519/925 | chr16 | 4362006 | ||
chr16:4362018
|
C | G | 1 | a0003c0019 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1545G>C | p.Leu515Leu | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/28 | 1623/3472 | 1545/2778 | 515/925 | chr16 | 4362018 | ||
chr16:4362694
|
C | T | 1 | a0005c0007 | 2 | HG03041.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.1320G>A | p.Thr440Thr | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 15/28 | 1398/3472 | 1320/2778 | 440/925 | chr16 | 4362694 | ||
chr16:4364327
|
G | A | 1 | a0001c0023 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1224C>T | p.Asp408Asp | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/28 | 1302/3472 | 1224/2778 | 408/925 | chr16 | 4364327 | ||
chr16:4364372
|
C | G | 1 | a0003c0018 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.1179G>C | p.Pro393Pro | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/28 | 1257/3472 | 1179/2778 | 393/925 | chr16 | 4364372 | ||
chr16:4395301
|
C | G | 1 | a0001c0014 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.603G>C | p.Pro201Pro | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/28 | 681/3472 | 603/2778 | 201/925 | chr16 | 4395301 | ||
chr16:4407594
|
G | A | 1 | a0008c0024 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.394C>T | p.Leu132Leu | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/28 | 472/3472 | 394/2778 | 132/925 | chr16 | 4407594 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:4354619
|
C | T | 6 | a0001c0002t0002a0002c0001t0002a0004c0005t0002others(3): Show | 51 | HG00544.hp1 HG00597.hp2 HG01074.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*539G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 28/28 | 539 | chr16 | 4354619 | |||||
chr16:4354728
|
G | A | 1 | a0018c0016t0003 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*430C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 28/28 | 430 | chr16 | 4354728 | |||||
chr16:4354856
|
G | A | 6 | a0001c0002t0002a0002c0001t0002a0004c0005t0002others(3): Show | 51 | HG00544.hp1 HG00597.hp2 HG01074.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*302C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 28/28 | 302 | chr16 | 4354856 | |||||
chr16:4355017
|
G | A | 1 | a0002c0001t0004 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*141C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 28/28 | 141 | chr16 | 4355017 | |||||
chr16:4416560
|
G | C | 1 | a0008c0024t0005 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/28 | 42 | chr16 | 4416560 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:4355237
|
T | G | 16 | a0003c0003t0001g0014a0003c0003t0001g0261a0003c0003t0001g0262others(13): Show | 17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.2772+49A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 27/27 | chr16 | 4355237 | ||||||
chr16:4355270
|
G | A | 3 | a0001c0002t0001g0088a0001c0002t0001g0090a0001c0002t0001g0130 | 3 | HG02258.hp2 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2772+16C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 27/27 | chr16 | 4355270 | ||||||
chr16:4355468
|
CT | C | 6 | a0002c0001t0001g0018a0002c0001t0001g0177a0002c0001t0001g0229others(3): Show | 6 | HG02897.hp2 HG03041.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2686-97delA | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355468 | ||||||
chr16:4355489
|
G | T | 39 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0029others(36): Show | 43 | HG00544.hp1 HG00597.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.2686-117C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355489 | ||||||
chr16:4355537
|
C | T | 1 | a0018c0016t0003g0259 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2686-165G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355537 | ||||||
chr16:4355538
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2686-166C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355538 | ||||||
chr16:4355606
|
T | C | 279 | a0001c0002t0001g0005a0001c0002t0001g0007a0001c0002t0001g0019others(276): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2686-234A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355606 | ||||||
chr16:4355636
|
T | G | 16 | a0003c0003t0001g0014a0003c0003t0001g0261a0003c0003t0001g0262others(13): Show | 17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.2686-264A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355636 | ||||||
chr16:4355659
|
G | C | 11 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(8): Show | 12 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2686-287C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355659 | ||||||
chr16:4355761
|
G | A | 3 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0023t0001g0040 | 3 | HG02922.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2686-389C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355761 | ||||||
chr16:4355778
|
G | A | 1 | a0001c0002t0001g0076 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2686-406C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355778 | ||||||
chr16:4355849
|
C | G | 1 | a0002c0001t0001g0141 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2686-477G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355849 | ||||||
chr16:4355858
|
G | A | 2 | a0002c0001t0001g0228a0002c0001t0001g0229 | 2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2686-486C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4355858 | ||||||
chr16:4356006
|
T | G | 1 | a0017c0020t0002g0046 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2686-634A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356006 | ||||||
chr16:4356223
|
G | A | 16 | a0003c0003t0001g0014a0003c0003t0001g0261a0003c0003t0001g0262others(13): Show | 17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.2686-851C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356223 | ||||||
chr16:4356273
|
A | T | 1 | a0002c0001t0001g0189 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2685+895T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356273 | ||||||
chr16:4356286
|
G | C | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2685+882C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356286 | ||||||
chr16:4356409
|
ATTTTATT others(5): Show |
A | 1 | a0002c0001t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2685+747_2685+758d others(14): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356409 | ||||||
chr16:4356501
|
C | T | 2 | a0002c0001t0001g0228a0002c0001t0001g0229 | 2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2685+667G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356501 | ||||||
chr16:4356502
|
G | A | 1 | a0001c0004t0001g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2685+666C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356502 | ||||||
chr16:4356622
|
G | A | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2685+546C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356622 | ||||||
chr16:4356633
|
G | A | 11 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(8): Show | 12 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2685+535C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356633 | ||||||
chr16:4356693
|
A | G | 1 | a0001c0002t0002g0035 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2685+475T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356693 | ||||||
chr16:4356784
|
G | A | 1 | a0001c0004t0001g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2685+384C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356784 | ||||||
chr16:4356984
|
C | A | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2685+184G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356984 | ||||||
chr16:4356984
|
C | T | 1 | a0004c0005t0002g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2685+184G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356984 | ||||||
chr16:4356992
|
G | A | 1 | a0001c0002t0001g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2685+176C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4356992 | ||||||
chr16:4357108
|
C | T | 1 | a0001c0004t0001g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2685+60G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 26/27 | chr16 | 4357108 | ||||||
chr16:4357292
|
C | A | 1 | a0001c0004t0001g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2594-33G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357292 | ||||||
chr16:4357346
|
T | C | 1 | a0001c0002t0002g0245 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2594-87A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357346 | ||||||
chr16:4357347
|
C | T | 1 | a0001c0002t0002g0245 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2594-88G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357347 | ||||||
chr16:4357351
|
CTTTCT | C | 48 | a0001c0002t0001g0039a0001c0002t0001g0086a0001c0002t0001g0275others(45): Show | 52 | HG00544.hp1 HG00597.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.2594-97_2594-93del others(5): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357351 | ||||||
chr16:4357355
|
CT | C | 89 | a0001c0002t0001g0005a0001c0002t0001g0007a0001c0002t0001g0020others(86): Show | 96 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.2594-97delA | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357355 | ||||||
chr16:4357355
|
CTT | C | 7 | a0001c0002t0001g0098a0001c0002t0001g0106a0001c0002t0001g0109others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2594-98_2594-97del others(2): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357355 | ||||||
chr16:4357360
|
T | C | 4 | a0003c0003t0001g0266a0003c0003t0001g0268a0003c0003t0001g0269others(1): Show | 4 | HG02809.hp1 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2594-101A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357360 | ||||||
chr16:4357463
|
G | A | 1 | a0001c0002t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2594-204C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357463 | ||||||
chr16:4357505
|
G | A | 1 | a0002c0001t0001g0195 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2594-246C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357505 | ||||||
chr16:4357513
|
C | T | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2594-254G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357513 | ||||||
chr16:4357602
|
C | T | 1 | a0002c0001t0001g0128 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2594-343G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357602 | ||||||
chr16:4357647
|
C | T | 3 | a0001c0002t0001g0108a0002c0001t0001g0221a0002c0001t0001g0242 | 3 | HG02040.hp1 NA18960.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.2593+321G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357647 | ||||||
chr16:4357743
|
C | G | 96 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(93): Show | 105 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.2593+225G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357743 | ||||||
chr16:4357752
|
C | CGT | 18 | a0001c0002t0002g0003a0003c0003t0001g0014a0003c0003t0001g0261others(15): Show | 21 | HG01074.hp1 HG01109.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.2593+214_2593+215d others(4): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357752 | ||||||
chr16:4357802
|
G | A | 1 | a0001c0004t0001g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2593+166C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 25/27 | chr16 | 4357802 | ||||||
chr16:4358266
|
A | G | 26 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(23): Show | 30 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.2457+101T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 24/27 | chr16 | 4358266 | ||||||
chr16:4358324
|
C | T | 7 | a0001c0004t0001g0001a0001c0004t0001g0008a0001c0004t0001g0041others(4): Show | 10 | HG02280.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2457+43G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 24/27 | chr16 | 4358324 | ||||||
chr16:4358587
|
C | T | 11 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(8): Show | 12 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2341-104G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4358587 | ||||||
chr16:4358590
|
G | A | 1 | a0001c0002t0002g0068 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2341-107C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4358590 | ||||||
chr16:4358591
|
G | A | 1 | a0001c0002t0002g0068 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2341-108C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4358591 | ||||||
chr16:4358940
|
C | T | 90 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(87): Show | 99 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.2340+356G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4358940 | ||||||
chr16:4359067
|
G | A | 3 | a0004c0005t0001g0256a0004c0005t0001g0257a0004c0005t0001g0258 | 3 | HG02895.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2340+229C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4359067 | ||||||
chr16:4359095
|
T | C | 2 | a0001c0002t0002g0075a0001c0002t0002g0092 | 2 | HG01515.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.2340+201A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4359095 | ||||||
chr16:4359275
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2340+21C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 23/27 | chr16 | 4359275 | ||||||
chr16:4359438
|
C | A | 1 | a0001c0002t0001g0028 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2250+42G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 22/27 | chr16 | 4359438 | ||||||
chr16:4359750
|
A | T | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2109-129T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4359750 | ||||||
chr16:4359878
|
T | G | 25 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0085others(22): Show | 31 | HG01099.hp1 HG01891.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.2109-257A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4359878 | ||||||
chr16:4359894
|
T | TATCTCCC others(91): Show |
3 | a0001c0002t0002g0048a0001c0002t0002g0121a0003c0003t0001g0276 | 3 | HG02717.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2108+286_2109-274d others(100): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4359894 | ||||||
chr16:4359968
|
A | ACCCCCCT others(92): Show |
1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2108+309_2108+310i others(101): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4359968 | ||||||
chr16:4359968
|
A | G | 4 | a0003c0003t0001g0261a0004c0005t0001g0256a0004c0005t0001g0257others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2108+310T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4359968 | ||||||
chr16:4360034
|
C | A | 1 | a0002c0001t0001g0196 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2108+244G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4360034 | ||||||
chr16:4360242
|
T | G | 35 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(32): Show | 37 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2108+36A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 21/27 | chr16 | 4360242 | ||||||
chr16:4360373
|
T | C | 12 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(9): Show | 13 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2023-10A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 20/27 | chr16 | 4360373 | ||||||
chr16:4360398
|
C | T | 3 | a0001c0002t0001g0088a0001c0002t0001g0090a0001c0002t0001g0130 | 3 | HG02258.hp2 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2023-35G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 20/27 | chr16 | 4360398 | ||||||
chr16:4360415
|
A | G | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2022+29T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 20/27 | chr16 | 4360415 | ||||||
chr16:4360429
|
C | T | 2 | a0001c0002t0001g0052a0001c0002t0001g0053 | 2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.2022+15G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 20/27 | chr16 | 4360429 | ||||||
chr16:4360658
|
T | TC | 3 | a0002c0001t0001g0209a0003c0003t0001g0263a0009c0008t0002g0059 | 3 | HG01928.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1918-111dupG | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/27 | chr16 | 4360658 | ||||||
chr16:4360684
|
GCCTCTCC others(14): Show |
G | 1 | a0002c0001t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1918-157_1918-137d others(23): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/27 | chr16 | 4360684 | ||||||
chr16:4360696
|
T | G | 1 | a0001c0004t0001g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1918-148A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/27 | chr16 | 4360696 | ||||||
chr16:4360866
|
TCACTGCT others(15): Show |
T | 109 | a0001c0002t0001g0019a0001c0002t0001g0027a0001c0002t0001g0030others(106): Show | 116 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1917+55_1917+76del others(22): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/27 | chr16 | 4360866 | ||||||
chr16:4360880
|
A | G | 1 | a0002c0001t0001g0175 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1917+63T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/27 | chr16 | 4360880 | ||||||
chr16:4360880
|
ACCTCTCC others(15): Show |
A | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1917+41_1917+62del others(22): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 19/27 | chr16 | 4360880 | ||||||
chr16:4361505
|
A | G | 29 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 31 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1579-36T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/27 | chr16 | 4361505 | ||||||
chr16:4361647
|
A | G | 10 | a0001c0004t0001g0001a0001c0004t0001g0008a0001c0004t0001g0041others(7): Show | 13 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1579-178T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/27 | chr16 | 4361647 | ||||||
chr16:4361696
|
C | T | 2 | a0001c0002t0001g0125a0002c0001t0001g0232 | 2 | HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1579-227G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/27 | chr16 | 4361696 | ||||||
chr16:4361700
|
G | A | 1 | a0002c0001t0001g0236 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1579-231C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/27 | chr16 | 4361700 | ||||||
chr16:4361911
|
G | A | 2 | a0001c0002t0001g0101a0002c0001t0001g0033 | 2 | HG01255.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1578+74C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 16/27 | chr16 | 4361911 | ||||||
chr16:4362478
|
T | C | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1402+134A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 15/27 | chr16 | 4362478 | ||||||
chr16:4362493
|
G | C | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1402+119C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 15/27 | chr16 | 4362493 | ||||||
chr16:4362596
|
C | T | 1 | a0001c0002t0002g0116 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1402+16G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 15/27 | chr16 | 4362596 | ||||||
chr16:4362597
|
G | A | 16 | a0003c0003t0001g0014a0003c0003t0001g0261a0003c0003t0001g0262others(13): Show | 17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1402+15C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 15/27 | chr16 | 4362597 | ||||||
chr16:4362805
|
C | T | 8 | a0001c0004t0001g0008a0001c0004t0001g0056a0001c0004t0001g0133others(5): Show | 9 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-67G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4362805 | ||||||
chr16:4362843
|
G | A | 1 | a0001c0002t0002g0006 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1276-105C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4362843 | ||||||
chr16:4362867
|
C | G | 139 | a0001c0002t0001g0019a0001c0002t0001g0027a0001c0002t0001g0030others(136): Show | 150 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1276-129G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4362867 | ||||||
chr16:4362880
|
G | A | 3 | a0001c0002t0001g0275a0005c0007t0001g0042a0005c0007t0001g0043 | 3 | HG03041.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1276-142C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4362880 | ||||||
chr16:4362920
|
C | T | 17 | a0003c0003t0001g0014a0003c0003t0001g0261a0003c0003t0001g0262others(14): Show | 18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1276-182G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4362920 | ||||||
chr16:4362939
|
A | G | 1 | a0015c0021t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1276-201T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4362939 | ||||||
chr16:4363081
|
A | G | 1 | a0002c0001t0001g0221 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1276-343T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363081 | ||||||
chr16:4363179
|
C | T | 16 | a0003c0003t0001g0014a0003c0003t0001g0261a0003c0003t0001g0262others(13): Show | 17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1276-441G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363179 | ||||||
chr16:4363328
|
A | G | 1 | a0001c0002t0002g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1276-590T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363328 | ||||||
chr16:4363432
|
C | T | 6 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(3): Show | 8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-694G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363432 | ||||||
chr16:4363515
|
G | GCCAACAT others(9): Show |
1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1275+745_1275+760d others(18): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363515 | ||||||
chr16:4363573
|
G | A | 1 | a0002c0001t0001g0177 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1275+703C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363573 | ||||||
chr16:4363729
|
A | C | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1275+547T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363729 | ||||||
chr16:4363780
|
A | G | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1275+496T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363780 | ||||||
chr16:4363781
|
G | C | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1275+495C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363781 | ||||||
chr16:4363817
|
G | A | 109 | a0001c0002t0001g0019a0001c0002t0001g0027a0001c0002t0001g0030others(106): Show | 118 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1275+459C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363817 | ||||||
chr16:4363837
|
G | A | 1 | a0017c0020t0002g0046 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+439C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363837 | ||||||
chr16:4363866
|
A | G | 1 | a0001c0004t0001g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1275+410T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4363866 | ||||||
chr16:4364072
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1275+204C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4364072 | ||||||
chr16:4364132
|
G | A | 1 | a0004c0005t0001g0257 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1275+144C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 14/27 | chr16 | 4364132 | ||||||
chr16:4364414
|
C | G | 1 | a0001c0002t0001g0090 | 1 | HG02258.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1138-1G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 13/27 | chr16 | 4364414 | ||||||
chr16:4364465
|
A | G | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1138-52T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 13/27 | chr16 | 4364465 | ||||||
chr16:4364466
|
G | A | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1138-53C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 13/27 | chr16 | 4364466 | ||||||
chr16:4364542
|
C | T | 4 | a0001c0004t0001g0008a0001c0004t0001g0133a0001c0004t0001g0135others(1): Show | 5 | HG02280.hp2 HG02886.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137+55G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 13/27 | chr16 | 4364542 | ||||||
chr16:4364691
|
T | A | 1 | a0002c0013t0001g0207 | 1 | NA18962.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1045-2A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 12/27 | chr16 | 4364691 | ||||||
chr16:4364693
|
G | T | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | splice_region_variant&intron_variant | LOW | c.1045-4C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 12/27 | chr16 | 4364693 | ||||||
chr16:4364726
|
G | A | 110 | a0001c0002t0001g0019a0001c0002t0001g0027a0001c0002t0001g0030others(107): Show | 118 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1045-37C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 12/27 | chr16 | 4364726 | ||||||
chr16:4364747
|
C | G | 1 | a0002c0001t0001g0163 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1044+28G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 12/27 | chr16 | 4364747 | ||||||
chr16:4364773
|
A | C | 1 | a0001c0002t0001g0125 | 1 | HG03654.hp1 | splice_donor_variant&intron_variant | HIGH | c.1044+2T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 12/27 | chr16 | 4364773 | ||||||
chr16:4364965
|
G | T | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.898+38C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 11/27 | chr16 | 4364965 | ||||||
chr16:4364986
|
G | A | 102 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0002t0001g0066others(99): Show | 109 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.898+17C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 11/27 | chr16 | 4364986 | ||||||
chr16:4365085
|
C | T | 1 | a0018c0016t0003g0259 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.841-25G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365085 | ||||||
chr16:4365268
|
C | G | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.841-208G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365268 | ||||||
chr16:4365268
|
C | T | 6 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(3): Show | 8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-208G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365268 | ||||||
chr16:4365269
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.841-209C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365269 | ||||||
chr16:4365272
|
G | T | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.841-212C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365272 | ||||||
chr16:4365310
|
G | A | 1 | a0001c0004t0001g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.840+181C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365310 | ||||||
chr16:4365376
|
G | C | 1 | a0001c0002t0002g0084 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.840+115C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365376 | ||||||
chr16:4365409
|
G | T | 137 | a0001c0002t0001g0019a0001c0002t0001g0027a0001c0002t0001g0030others(134): Show | 148 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.840+82C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365409 | ||||||
chr16:4365454
|
C | G | 141 | a0001c0002t0001g0019a0001c0002t0001g0027a0001c0002t0001g0030others(138): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.840+37G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365454 | ||||||
chr16:4365466
|
G | C | 1 | a0001c0002t0002g0068 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.840+25C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365466 | ||||||
chr16:4365474
|
C | A | 3 | a0001c0002t0001g0051a0001c0002t0001g0131a0001c0002t0001g0138 | 3 | HG01243.hp2 HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.840+17G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 10/27 | chr16 | 4365474 | ||||||
chr16:4365695
|
C | G | 133 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0002t0001g0049others(130): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.786-150G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4365695 | ||||||
chr16:4365726
|
C | T | 3 | a0002c0001t0001g0164a0002c0001t0001g0165a0002c0001t0001g0166 | 3 | HG01106.hp2 HG01168.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.786-181G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4365726 | ||||||
chr16:4365755
|
G | C | 17 | a0003c0003t0001g0014a0003c0003t0001g0261a0003c0003t0001g0262others(14): Show | 18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.786-210C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4365755 | ||||||
chr16:4365774
|
C | T | 2 | a0003c0003t0001g0271a0003c0003t0001g0273 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.786-229G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4365774 | ||||||
chr16:4365918
|
G | A | 5 | a0002c0001t0001g0009a0002c0001t0001g0140a0002c0001t0001g0177others(2): Show | 6 | HG00423.hp2 HG00597.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.786-373C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4365918 | ||||||
chr16:4366054
|
C | T | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.786-509G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366054 | ||||||
chr16:4366100
|
C | T | 17 | a0003c0003t0001g0014a0003c0003t0001g0261a0003c0003t0001g0262others(14): Show | 18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.786-555G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366100 | ||||||
chr16:4366138
|
C | T | 1 | a0002c0001t0001g0224 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.786-593G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366138 | ||||||
chr16:4366140
|
C | G | 18 | a0001c0002t0001g0034a0003c0003t0001g0014a0003c0003t0001g0261others(15): Show | 19 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.786-595G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366140 | ||||||
chr16:4366211
|
G | A | 3 | a0001c0002t0001g0051a0001c0002t0001g0131a0001c0002t0001g0138 | 3 | HG01243.hp2 HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.786-666C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366211 | ||||||
chr16:4366228
|
T | C | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.786-683A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366228 | ||||||
chr16:4366229
|
C | T | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.786-684G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366229 | ||||||
chr16:4366316
|
G | A | 9 | a0001c0004t0001g0008a0001c0004t0001g0056a0001c0004t0001g0133others(6): Show | 10 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.786-771C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366316 | ||||||
chr16:4366362
|
C | CA | 29 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 31 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.786-818_786-817ins others(1): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366362 | ||||||
chr16:4366497
|
C | T | 12 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(9): Show | 13 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.786-952G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366497 | ||||||
chr16:4366535
|
C | CT | 18 | a0001c0002t0001g0034a0001c0002t0001g0107a0001c0002t0001g0108others(15): Show | 20 | HG01099.hp1 HG02055.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.786-991dupA | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366535 | ||||||
chr16:4366535
|
C | CTT | 27 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(24): Show | 29 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.786-992_786-991dup others(2): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366535 | ||||||
chr16:4366535
|
CT | C | 18 | a0001c0002t0001g0103a0001c0002t0001g0106a0001c0002t0001g0111others(15): Show | 18 | HG01070.hp2 HG01099.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.786-991delA | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366535 | ||||||
chr16:4366697
|
T | G | 2 | a0001c0002t0002g0084a0003c0018t0001g0277 | 2 | HG02897.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.786-1152A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366697 | ||||||
chr16:4366857
|
C | G | 12 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(9): Show | 13 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.786-1312G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366857 | ||||||
chr16:4366872
|
C | T | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.786-1327G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366872 | ||||||
chr16:4366873
|
T | G | 1 | a0003c0018t0001g0277 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.786-1328A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366873 | ||||||
chr16:4366916
|
C | T | 16 | a0003c0003t0001g0014a0003c0003t0001g0261a0003c0003t0001g0262others(13): Show | 17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.786-1371G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366916 | ||||||
chr16:4366921
|
C | T | 12 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(9): Show | 13 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.786-1376G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366921 | ||||||
chr16:4366981
|
C | T | 1 | a0001c0002t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.786-1436G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4366981 | ||||||
chr16:4367159
|
G | C | 29 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 31 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.786-1614C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367159 | ||||||
chr16:4367179
|
C | A | 29 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 31 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.786-1634G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367179 | ||||||
chr16:4367252
|
A | T | 29 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 31 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.786-1707T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367252 | ||||||
chr16:4367261
|
C | T | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.786-1716G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367261 | ||||||
chr16:4367337
|
T | C | 29 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 31 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.786-1792A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367337 | ||||||
chr16:4367390
|
C | T | 2 | a0001c0002t0002g0054a0001c0002t0002g0055 | 2 | HG01934.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.786-1845G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367390 | ||||||
chr16:4367418
|
G | A | 1 | a0018c0016t0003g0259 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.786-1873C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367418 | ||||||
chr16:4367627
|
C | A | 1 | a0001c0002t0002g0006 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.786-2082G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367627 | ||||||
chr16:4367796
|
A | C | 29 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(26): Show | 31 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.786-2251T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367796 | ||||||
chr16:4367887
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.786-2342G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367887 | ||||||
chr16:4367981
|
T | C | 1 | a0002c0001t0001g0159 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.786-2436A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4367981 | ||||||
chr16:4368067
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.786-2522G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368067 | ||||||
chr16:4368146
|
A | C | 2 | a0002c0001t0001g0228a0002c0001t0001g0229 | 2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.786-2601T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368146 | ||||||
chr16:4368238
|
T | C | 1 | a0001c0002t0002g0068 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.786-2693A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368238 | ||||||
chr16:4368284
|
T | C | 18 | a0001c0002t0001g0051a0001c0002t0001g0131a0003c0003t0001g0014others(15): Show | 19 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.786-2739A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368284 | ||||||
chr16:4368303
|
C | G | 1 | a0001c0002t0001g0025 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.786-2758G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368303 | ||||||
chr16:4368308
|
A | G | 1 | a0001c0004t0001g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.786-2763T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368308 | ||||||
chr16:4368406
|
G | A | 1 | a0002c0001t0001g0196 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.786-2861C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368406 | ||||||
chr16:4368412
|
C | G | 1 | a0002c0001t0001g0204 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.786-2867G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368412 | ||||||
chr16:4368650
|
A | G | 1 | a0001c0004t0001g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.786-3105T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368650 | ||||||
chr16:4368653
|
C | T | 1 | a0001c0002t0002g0065 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.786-3108G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368653 | ||||||
chr16:4368747
|
C | CA | 13 | a0001c0002t0001g0034a0001c0002t0001g0038a0001c0002t0001g0053others(10): Show | 13 | HG01099.hp1 HG01884.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.786-3203dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368747 | ||||||
chr16:4368747
|
C | CAA | 8 | a0001c0002t0002g0079a0001c0004t0001g0008a0001c0004t0001g0056others(5): Show | 9 | HG01891.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.786-3204_786-3203d others(4): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368747 | ||||||
chr16:4368747
|
C | CAAA | 12 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(9): Show | 13 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.786-3205_786-3203d others(5): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368747 | ||||||
chr16:4368747
|
CA | C | 9 | a0001c0002t0002g0062a0001c0002t0002g0084a0002c0001t0001g0164others(6): Show | 9 | HG00673.hp2 HG01069.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.786-3203delT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368747 | ||||||
chr16:4368781
|
G | A | 1 | a0002c0001t0001g0226 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.786-3236C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368781 | ||||||
chr16:4368834
|
C | T | 11 | a0001c0002t0001g0088a0001c0002t0001g0090a0001c0002t0001g0114others(8): Show | 12 | HG01074.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.786-3289G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368834 | ||||||
chr16:4368996
|
T | C | 1 | a0001c0002t0002g0089 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.786-3451A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4368996 | ||||||
chr16:4369021
|
C | T | 1 | a0002c0001t0001g0228 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.786-3476G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369021 | ||||||
chr16:4369034
|
G | T | 1 | a0002c0001t0001g0221 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.786-3489C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369034 | ||||||
chr16:4369120
|
T | G | 30 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(27): Show | 32 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.786-3575A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369120 | ||||||
chr16:4369206
|
T | A | 8 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(5): Show | 9 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.786-3661A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369206 | ||||||
chr16:4369314
|
G | A | 11 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(8): Show | 12 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.786-3769C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369314 | ||||||
chr16:4369323
|
G | C | 16 | a0003c0003t0001g0014a0003c0003t0001g0261a0003c0003t0001g0262others(13): Show | 17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.786-3778C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369323 | ||||||
chr16:4369344
|
T | C | 34 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(31): Show | 36 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.786-3799A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369344 | ||||||
chr16:4369463
|
G | A | 2 | a0001c0002t0002g0079a0002c0001t0002g0278 | 2 | NA18943.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.786-3918C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369463 | ||||||
chr16:4369511
|
G | C | 1 | a0001c0002t0001g0024 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.786-3966C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369511 | ||||||
chr16:4369557
|
C | T | 1 | a0004c0005t0002g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.786-4012G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369557 | ||||||
chr16:4369614
|
C | A | 11 | a0001c0002t0001g0088a0001c0002t0001g0090a0001c0002t0001g0114others(8): Show | 12 | HG01074.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.786-4069G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369614 | ||||||
chr16:4369853
|
C | T | 2 | a0002c0001t0001g0159a0002c0001t0001g0230 | 2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.786-4308G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4369853 | ||||||
chr16:4370280
|
G | C | 16 | a0003c0003t0001g0014a0003c0003t0001g0261a0003c0003t0001g0262others(13): Show | 17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.786-4735C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370280 | ||||||
chr16:4370372
|
T | C | 2 | a0002c0001t0001g0199a0002c0001t0001g0200 | 2 | HG02015.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.786-4827A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370372 | ||||||
chr16:4370645
|
A | G | 1 | a0002c0001t0001g0255 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.786-5100T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370645 | ||||||
chr16:4370646
|
G | A | 1 | a0002c0001t0001g0255 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.786-5101C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370646 | ||||||
chr16:4370647
|
A | T | 1 | a0002c0001t0001g0255 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.786-5102T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370647 | ||||||
chr16:4370694
|
C | T | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.786-5149G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370694 | ||||||
chr16:4370786
|
T | C | 150 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0002t0001g0049others(147): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.786-5241A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370786 | ||||||
chr16:4370816
|
G | GC | 121 | a0001c0002t0001g0049a0001c0002t0001g0052a0001c0002t0001g0053others(118): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.786-5272dupG | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370816 | ||||||
chr16:4370874
|
G | C | 4 | a0002c0001t0001g0186a0002c0001t0001g0187a0002c0001t0001g0188others(1): Show | 4 | HG00741.hp1 HG01123.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.786-5329C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370874 | ||||||
chr16:4370954
|
A | G | 16 | a0003c0003t0001g0014a0003c0003t0001g0261a0003c0003t0001g0262others(13): Show | 17 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.786-5409T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370954 | ||||||
chr16:4370957
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786-5412C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4370957 | ||||||
chr16:4371026
|
G | A | 4 | a0001c0002t0001g0275a0005c0007t0001g0042a0005c0007t0001g0043others(1): Show | 4 | HG03041.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.786-5481C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371026 | ||||||
chr16:4371124
|
T | A | 2 | a0001c0002t0001g0049a0002c0001t0001g0218 | 2 | NA18966.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.786-5579A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371124 | ||||||
chr16:4371125
|
C | G | 6 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(3): Show | 8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.786-5580G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371125 | ||||||
chr16:4371189
|
C | T | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786-5644G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371189 | ||||||
chr16:4371233
|
T | G | 13 | a0001c0002t0001g0275a0001c0004t0001g0008a0001c0004t0001g0056others(10): Show | 14 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.786-5688A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371233 | ||||||
chr16:4371315
|
A | G | 1 | a0002c0001t0004g0192 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.786-5770T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371315 | ||||||
chr16:4371602
|
C | CTGTAAAA others(6): Show |
1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.786-6058_786-6057i others(15): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371602 | ||||||
chr16:4371603
|
G | C | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.786-6058C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371603 | ||||||
chr16:4371685
|
G | A | 1 | a0018c0016t0003g0259 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.786-6140C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371685 | ||||||
chr16:4371822
|
A | G | 1 | a0002c0001t0001g0184 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.786-6277T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371822 | ||||||
chr16:4371931
|
C | G | 4 | a0001c0002t0001g0275a0005c0007t0001g0042a0005c0007t0001g0043others(1): Show | 4 | HG03041.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.786-6386G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4371931 | ||||||
chr16:4372121
|
A | G | 197 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(194): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.786-6576T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372121 | ||||||
chr16:4372124
|
C | G | 1 | a0018c0016t0003g0259 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.786-6579G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372124 | ||||||
chr16:4372192
|
G | A | 1 | a0002c0001t0001g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.786-6647C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372192 | ||||||
chr16:4372304
|
G | A | 152 | a0001c0002t0001g0019a0001c0002t0001g0027a0001c0002t0001g0030others(149): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.786-6759C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372304 | ||||||
chr16:4372385
|
C | T | 6 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(3): Show | 8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.786-6840G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372385 | ||||||
chr16:4372515
|
C | T | 1 | a0001c0002t0002g0121 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.786-6970G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372515 | ||||||
chr16:4372606
|
G | T | 152 | a0001c0002t0001g0019a0001c0002t0001g0027a0001c0002t0001g0030others(149): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.786-7061C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372606 | ||||||
chr16:4372646
|
G | C | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.786-7101C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372646 | ||||||
chr16:4372743
|
A | G | 32 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(29): Show | 34 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.786-7198T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372743 | ||||||
chr16:4372759
|
C | A | 1 | a0002c0001t0001g0016 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.786-7214G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372759 | ||||||
chr16:4372825
|
G | A | 20 | a0002c0001t0001g0011a0002c0001t0001g0071a0002c0001t0001g0087others(17): Show | 21 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.786-7280C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372825 | ||||||
chr16:4372911
|
G | C | 34 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(31): Show | 36 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.786-7366C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4372911 | ||||||
chr16:4373020
|
G | A | 1 | a0001c0002t0002g0116 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.786-7475C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373020 | ||||||
chr16:4373282
|
C | T | 1 | a0001c0002t0001g0104 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.786-7737G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373282 | ||||||
chr16:4373314
|
C | A | 2 | a0001c0002t0001g0275a0018c0016t0003g0259 | 2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.786-7769G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373314 | ||||||
chr16:4373367
|
T | C | 196 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(193): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.786-7822A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373367 | ||||||
chr16:4373577
|
G | C | 1 | a0002c0001t0001g0177 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.786-8032C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373577 | ||||||
chr16:4373613
|
G | A | 1 | a0002c0001t0001g0227 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.786-8068C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373613 | ||||||
chr16:4373632
|
G | A | 2 | a0001c0002t0002g0245a0001c0002t0002g0246 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.786-8087C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373632 | ||||||
chr16:4373643
|
C | T | 11 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(8): Show | 12 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.786-8098G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373643 | ||||||
chr16:4373685
|
A | G | 1 | a0001c0002t0001g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.786-8140T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373685 | ||||||
chr16:4373703
|
A | T | 1 | a0014c0017t0001g0077 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.786-8158T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373703 | ||||||
chr16:4373801
|
C | T | 2 | a0002c0001t0001g0240a0002c0001t0001g0241 | 2 | NA18980.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.786-8256G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373801 | ||||||
chr16:4373863
|
C | T | 1 | a0002c0001t0001g0211 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.786-8318G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373863 | ||||||
chr16:4373892
|
C | G | 1 | a0001c0002t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.786-8347G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373892 | ||||||
chr16:4373982
|
C | T | 8 | a0001c0004t0001g0008a0001c0004t0001g0133a0001c0004t0001g0134others(5): Show | 9 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.786-8437G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373982 | ||||||
chr16:4373995
|
T | C | 1 | a0001c0002t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.786-8450A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4373995 | ||||||
chr16:4374086
|
C | CGT | 31 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(28): Show | 34 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.786-8543_786-8542d others(4): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374086 | ||||||
chr16:4374086
|
C | CGTGTGTG others(13): Show |
2 | a0001c0002t0001g0275a0018c0016t0003g0259 | 2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.786-8561_786-8542d others(22): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374086 | ||||||
chr16:4374142
|
G | A | 1 | a0002c0001t0001g0173 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.786-8597C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374142 | ||||||
chr16:4374260
|
C | T | 1 | a0001c0002t0001g0099 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.786-8715G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374260 | ||||||
chr16:4374300
|
C | T | 1 | a0002c0001t0001g0252 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.786-8755G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374300 | ||||||
chr16:4374321
|
C | T | 1 | a0017c0020t0002g0046 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.786-8776G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374321 | ||||||
chr16:4374387
|
C | A | 1 | a0019c0015t0001g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.786-8842G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374387 | ||||||
chr16:4374449
|
C | T | 1 | a0001c0002t0002g0094 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.786-8904G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374449 | ||||||
chr16:4374540
|
G | A | 2 | a0001c0002t0002g0037a0001c0002t0002g0116 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.786-8995C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374540 | ||||||
chr16:4374551
|
G | T | 1 | a0004c0005t0001g0257 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.786-9006C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374551 | ||||||
chr16:4374680
|
C | G | 1 | a0002c0001t0001g0177 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.786-9135G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374680 | ||||||
chr16:4374910
|
G | C | 1 | a0001c0002t0002g0084 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.786-9365C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374910 | ||||||
chr16:4374915
|
T | G | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.786-9370A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374915 | ||||||
chr16:4374995
|
C | G | 2 | a0001c0002t0001g0103a0002c0001t0001g0178 | 2 | NA19055.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.786-9450G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4374995 | ||||||
chr16:4375010
|
G | A | 1 | a0002c0001t0001g0254 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.786-9465C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375010 | ||||||
chr16:4375073
|
C | T | 1 | a0001c0002t0002g0055 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.786-9528G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375073 | ||||||
chr16:4375121
|
C | T | 1 | a0001c0002t0002g0116 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.786-9576G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375121 | ||||||
chr16:4375440
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.786-9895C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375440 | ||||||
chr16:4375491
|
ATTC | A | 10 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(7): Show | 11 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.786-9949_786-9947d others(5): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375491 | ||||||
chr16:4375527
|
A | G | 191 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(188): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.786-9982T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375527 | ||||||
chr16:4375729
|
C | T | 1 | a0001c0002t0002g0080 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.786-10184G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375729 | ||||||
chr16:4375730
|
G | A | 2 | a0002c0001t0001g0198a0002c0001t0002g0278 | 2 | HG01123.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.786-10185C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375730 | ||||||
chr16:4375783
|
C | T | 1 | a0001c0002t0002g0065 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.786-10238G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4375783 | ||||||
chr16:4376072
|
C | T | 1 | a0002c0001t0001g0142 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.786-10527G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376072 | ||||||
chr16:4376107
|
A | G | 1 | a0001c0002t0001g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.786-10562T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376107 | ||||||
chr16:4376114
|
G | A | 1 | a0001c0004t0001g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.786-10569C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376114 | ||||||
chr16:4376188
|
C | T | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786-10643G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376188 | ||||||
chr16:4376408
|
C | T | 11 | a0001c0002t0001g0051a0001c0004t0001g0008a0001c0004t0001g0133others(8): Show | 12 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.786-10863G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376408 | ||||||
chr16:4376563
|
T | G | 189 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(186): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.786-11018A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376563 | ||||||
chr16:4376573
|
G | A | 1 | a0002c0001t0001g0157 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.786-11028C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376573 | ||||||
chr16:4376761
|
C | T | 1 | a0001c0002t0001g0024 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.786-11216G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4376761 | ||||||
chr16:4377009
|
G | C | 160 | a0001c0002t0001g0019a0001c0002t0001g0034a0001c0002t0001g0038others(157): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.785+10977C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377009 | ||||||
chr16:4377142
|
C | T | 11 | a0001c0002t0001g0051a0001c0004t0001g0008a0001c0004t0001g0133others(8): Show | 12 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.785+10844G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377142 | ||||||
chr16:4377214
|
C | T | 1 | a0018c0016t0003g0259 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.785+10772G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377214 | ||||||
chr16:4377234
|
T | A | 1 | a0004c0005t0002g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.785+10752A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377234 | ||||||
chr16:4377235
|
C | A | 1 | a0004c0005t0002g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.785+10751G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377235 | ||||||
chr16:4377429
|
C | G | 9 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(6): Show | 11 | HG02280.hp1 HG02486.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.785+10557G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377429 | ||||||
chr16:4377443
|
G | A | 13 | a0003c0003t0001g0014a0003c0003t0001g0264a0003c0003t0001g0265others(10): Show | 14 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.785+10543C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377443 | ||||||
chr16:4377618
|
G | A | 1 | a0001c0004t0001g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.785+10368C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377618 | ||||||
chr16:4377736
|
T | C | 1 | a0015c0021t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.785+10250A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377736 | ||||||
chr16:4377782
|
A | C | 182 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(179): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.785+10204T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377782 | ||||||
chr16:4377793
|
G | A | 1 | a0001c0004t0001g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.785+10193C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377793 | ||||||
chr16:4377796
|
T | C | 2 | a0001c0002t0002g0080a0001c0002t0002g0081 | 2 | HG02027.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.785+10190A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377796 | ||||||
chr16:4377824
|
A | C | 1 | a0001c0002t0001g0057 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.785+10162T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377824 | ||||||
chr16:4377860
|
C | T | 9 | a0001c0002t0001g0051a0001c0004t0001g0008a0001c0004t0001g0133others(6): Show | 10 | HG01099.hp1 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.785+10126G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377860 | ||||||
chr16:4377929
|
G | A | 1 | a0001c0004t0001g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.785+10057C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377929 | ||||||
chr16:4377958
|
C | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0021a0001c0002t0001g0022others(1): Show | 5 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+10028G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4377958 | ||||||
chr16:4378132
|
C | T | 1 | a0002c0001t0001g0163 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.785+9854G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378132 | ||||||
chr16:4378250
|
G | A | 25 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(22): Show | 27 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.785+9736C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378250 | ||||||
chr16:4378309
|
C | T | 1 | a0003c0003t0001g0265 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.785+9677G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378309 | ||||||
chr16:4378328
|
C | CGGCCACA others(23): Show |
2 | a0001c0002t0001g0145a0001c0002t0001g0148 | 2 | HG01074.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.785+9628_785+9657d others(32): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378328 | ||||||
chr16:4378494
|
T | C | 8 | a0002c0001t0001g0119a0002c0001t0001g0120a0002c0001t0001g0132others(5): Show | 8 | HG02055.hp2 HG02258.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.785+9492A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378494 | ||||||
chr16:4378555
|
C | T | 1 | a0001c0002t0001g0020 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.785+9431G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378555 | ||||||
chr16:4378652
|
G | A | 1 | a0002c0001t0004g0192 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.785+9334C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378652 | ||||||
chr16:4378883
|
G | A | 141 | a0001c0002t0001g0005a0001c0002t0001g0007a0001c0002t0001g0020others(138): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.785+9103C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378883 | ||||||
chr16:4378961
|
C | T | 2 | a0001c0002t0002g0047a0001c0002t0002g0251 | 2 | NA18977.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.785+9025G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4378961 | ||||||
chr16:4379106
|
C | T | 134 | a0001c0002t0001g0019a0001c0002t0001g0039a0001c0002t0001g0049others(131): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.785+8880G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379106 | ||||||
chr16:4379320
|
T | G | 2 | a0001c0002t0001g0052a0001c0002t0001g0053 | 2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.785+8666A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379320 | ||||||
chr16:4379324
|
G | A | 2 | a0001c0002t0002g0048a0001c0002t0002g0121 | 2 | HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.785+8662C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379324 | ||||||
chr16:4379392
|
C | G | 178 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(175): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.785+8594G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379392 | ||||||
chr16:4379711
|
C | T | 1 | a0002c0001t0001g0163 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.785+8275G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379711 | ||||||
chr16:4379730
|
C | A | 1 | a0001c0002t0001g0076 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.785+8256G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379730 | ||||||
chr16:4379880
|
T | TA | 142 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(139): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.785+8105dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379880 | ||||||
chr16:4379880
|
TA | T | 10 | a0001c0002t0001g0051a0001c0002t0001g0105a0001c0002t0001g0107others(7): Show | 10 | HG01884.hp2 HG02622.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.785+8105delT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379880 | ||||||
chr16:4379882
|
A | C | 2 | a0001c0002t0001g0052a0001c0002t0001g0053 | 2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.785+8104T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379882 | ||||||
chr16:4379901
|
T | A | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.785+8085A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379901 | ||||||
chr16:4379916
|
TGCATGGT others(5): Show |
T | 143 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(140): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.785+8058_785+8069d others(14): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4379916 | ||||||
chr16:4380057
|
C | CA | 8 | a0001c0002t0001g0053a0001c0002t0001g0058a0001c0002t0001g0105others(5): Show | 9 | HG00280.hp2 HG01099.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.785+7928dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380057 | ||||||
chr16:4380172
|
C | G | 12 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(9): Show | 13 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.785+7814G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380172 | ||||||
chr16:4380368
|
C | T | 1 | a0001c0002t0001g0099 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.785+7618G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380368 | ||||||
chr16:4380369
|
G | A | 1 | a0001c0002t0001g0169 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.785+7617C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380369 | ||||||
chr16:4380395
|
G | A | 2 | a0002c0001t0001g0158a0002c0001t0001g0193 | 2 | HG02735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.785+7591C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380395 | ||||||
chr16:4380421
|
C | T | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.785+7565G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380421 | ||||||
chr16:4380480
|
C | G | 12 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(9): Show | 13 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.785+7506G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380480 | ||||||
chr16:4380630
|
C | T | 1 | a0001c0002t0001g0099 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.785+7356G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380630 | ||||||
chr16:4380660
|
C | T | 4 | a0001c0004t0001g0008a0001c0004t0001g0133a0001c0004t0001g0135others(1): Show | 5 | HG02280.hp2 HG02886.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+7326G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380660 | ||||||
chr16:4380727
|
C | T | 4 | a0001c0002t0001g0005a0001c0002t0001g0021a0001c0002t0001g0022others(1): Show | 5 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+7259G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380727 | ||||||
chr16:4380909
|
T | C | 1 | a0002c0001t0001g0223 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.785+7077A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380909 | ||||||
chr16:4380917
|
C | T | 1 | a0002c0001t0001g0223 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.785+7069G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380917 | ||||||
chr16:4380955
|
C | T | 1 | a0001c0002t0001g0169 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.785+7031G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4380955 | ||||||
chr16:4381025
|
G | T | 1 | a0001c0002t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.785+6961C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381025 | ||||||
chr16:4381201
|
A | G | 184 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(181): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.785+6785T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381201 | ||||||
chr16:4381255
|
C | T | 1 | a0001c0002t0002g0055 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.785+6731G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381255 | ||||||
chr16:4381264
|
C | T | 1 | a0002c0001t0001g0036 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.785+6722G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381264 | ||||||
chr16:4381359
|
G | A | 6 | a0002c0001t0001g0162a0002c0001t0001g0164a0002c0001t0001g0165others(3): Show | 6 | HG01106.hp2 HG01168.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.785+6627C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381359 | ||||||
chr16:4381372
|
G | C | 4 | a0002c0001t0001g0045a0002c0001t0001g0194a0002c0001t0001g0210others(1): Show | 4 | HG00140.hp1 HG00639.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.785+6614C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381372 | ||||||
chr16:4381464
|
C | T | 1 | a0001c0002t0001g0106 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.785+6522G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381464 | ||||||
chr16:4381582
|
C | T | 3 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0014t0001g0026 | 3 | HG01891.hp1 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.785+6404G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381582 | ||||||
chr16:4381879
|
C | T | 6 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(3): Show | 8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.785+6107G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381879 | ||||||
chr16:4381909
|
C | T | 1 | a0002c0001t0001g0140 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.785+6077G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4381909 | ||||||
chr16:4382028
|
A | C | 184 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(181): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.785+5958T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382028 | ||||||
chr16:4382163
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.785+5823G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382163 | ||||||
chr16:4382234
|
C | G | 1 | a0002c0001t0001g0221 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.785+5752G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382234 | ||||||
chr16:4382467
|
T | C | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.785+5519A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382467 | ||||||
chr16:4382506
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.785+5480C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382506 | ||||||
chr16:4382569
|
C | T | 1 | a0001c0004t0001g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.785+5417G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382569 | ||||||
chr16:4382643
|
C | T | 1 | a0004c0005t0002g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.785+5343G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382643 | ||||||
chr16:4382664
|
C | T | 1 | a0002c0001t0001g0254 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.785+5322G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4382664 | ||||||
chr16:4383015
|
G | A | 17 | a0001c0002t0002g0267a0003c0003t0001g0014a0003c0003t0001g0261others(14): Show | 18 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.785+4971C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383015 | ||||||
chr16:4383170
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.785+4816G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383170 | ||||||
chr16:4383497
|
T | C | 1 | a0001c0004t0001g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.785+4489A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383497 | ||||||
chr16:4383602
|
CA | C | 41 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(38): Show | 44 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.785+4383delT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383602 | ||||||
chr16:4383606
|
GC | G | 149 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(146): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.785+4379delG | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383606 | ||||||
chr16:4383607
|
C | G | 41 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(38): Show | 44 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.785+4379G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383607 | ||||||
chr16:4383734
|
A | G | 278 | a0001c0002t0001g0005a0001c0002t0001g0007a0001c0002t0001g0019others(275): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.785+4252T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383734 | ||||||
chr16:4383779
|
G | T | 8 | a0001c0002t0001g0201a0002c0001t0001g0010a0002c0001t0001g0170others(5): Show | 9 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.785+4207C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383779 | ||||||
chr16:4383918
|
G | C | 1 | a0001c0002t0002g0231 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.785+4068C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4383918 | ||||||
chr16:4384197
|
T | C | 190 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(187): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.785+3789A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384197 | ||||||
chr16:4384373
|
G | A | 190 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(187): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.785+3613C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384373 | ||||||
chr16:4384475
|
A | C | 5 | a0004c0005t0001g0256a0004c0005t0001g0257a0004c0005t0001g0258others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+3511T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384475 | ||||||
chr16:4384600
|
G | A | 1 | a0002c0001t0001g0033 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.785+3386C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384600 | ||||||
chr16:4384694
|
G | C | 5 | a0001c0002t0001g0088a0001c0002t0001g0090a0001c0002t0001g0130others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+3292C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384694 | ||||||
chr16:4384706
|
C | T | 1 | a0001c0002t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.785+3280G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384706 | ||||||
chr16:4384732
|
T | A | 1 | a0001c0002t0001g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.785+3254A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384732 | ||||||
chr16:4384810
|
C | T | 1 | a0002c0001t0001g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.785+3176G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384810 | ||||||
chr16:4384871
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.785+3115C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4384871 | ||||||
chr16:4385107
|
C | T | 2 | a0001c0002t0002g0047a0001c0002t0002g0251 | 2 | NA18977.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.785+2879G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4385107 | ||||||
chr16:4385162
|
G | C | 136 | a0001c0002t0001g0049a0001c0002t0001g0082a0001c0002t0001g0145others(133): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.785+2824C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4385162 | ||||||
chr16:4385356
|
G | A | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.785+2630C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4385356 | ||||||
chr16:4385379
|
T | A | 1 | a0001c0002t0001g0101 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.785+2607A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4385379 | ||||||
chr16:4385556
|
TG | T | 7 | a0001c0002t0001g0145a0001c0002t0001g0146a0001c0002t0001g0147others(4): Show | 7 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+2429delC | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4385556 | ||||||
chr16:4386278
|
T | G | 1 | a0001c0002t0002g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.785+1708A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386278 | ||||||
chr16:4386380
|
C | A | 1 | a0001c0002t0001g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.785+1606G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386380 | ||||||
chr16:4386444
|
A | G | 250 | a0001c0002t0001g0005a0001c0002t0001g0007a0001c0002t0001g0019others(247): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.785+1542T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386444 | ||||||
chr16:4386551
|
G | A | 5 | a0001c0002t0001g0102a0001c0002t0001g0103a0001c0002t0001g0109others(2): Show | 7 | HG01074.hp1 HG01109.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+1435C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386551 | ||||||
chr16:4386577
|
G | A | 20 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(17): Show | 22 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.785+1409C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386577 | ||||||
chr16:4386706
|
C | A | 5 | a0001c0002t0001g0088a0001c0002t0001g0090a0001c0002t0001g0130others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+1280G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386706 | ||||||
chr16:4386780
|
G | A | 1 | a0001c0002t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.785+1206C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386780 | ||||||
chr16:4386840
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.785+1146C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386840 | ||||||
chr16:4386840
|
G | C | 8 | a0001c0002t0001g0145a0001c0002t0001g0146a0001c0002t0001g0147others(5): Show | 8 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.785+1146C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386840 | ||||||
chr16:4386902
|
G | A | 1 | a0002c0001t0001g0180 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.785+1084C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4386902 | ||||||
chr16:4387003
|
A | G | 1 | a0001c0002t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.785+983T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387003 | ||||||
chr16:4387153
|
C | T | 3 | a0001c0002t0002g0048a0001c0002t0002g0121a0001c0002t0002g0161 | 3 | HG02717.hp1 HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.785+833G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387153 | ||||||
chr16:4387253
|
G | A | 2 | a0001c0002t0002g0083a0001c0002t0002g0084 | 2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.785+733C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387253 | ||||||
chr16:4387419
|
G | A | 1 | a0002c0001t0001g0200 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.785+567C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387419 | ||||||
chr16:4387491
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.785+495C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387491 | ||||||
chr16:4387523
|
CCCACCTC others(5): Show |
C | 1 | a0002c0001t0001g0254 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.785+451_785+462del others(12): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387523 | ||||||
chr16:4387539
|
C | T | 1 | a0001c0002t0001g0250 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.785+447G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387539 | ||||||
chr16:4387725
|
C | T | 5 | a0004c0005t0001g0256a0004c0005t0001g0257a0004c0005t0001g0258others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+261G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387725 | ||||||
chr16:4387824
|
G | T | 20 | a0001c0002t0001g0086a0001c0002t0002g0267a0003c0003t0001g0014others(17): Show | 21 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.785+162C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387824 | ||||||
chr16:4387830
|
G | A | 4 | a0002c0001t0001g0184a0002c0001t0001g0185a0002c0001t0001g0228others(1): Show | 4 | NA18969.hp2 NA18977.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.785+156C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387830 | ||||||
chr16:4387869
|
G | T | 4 | a0001c0002t0001g0034a0001c0002t0001g0051a0001c0004t0001g0244others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+117C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 9/27 | chr16 | 4387869 | ||||||
chr16:4388082
|
G | A | 1 | a0002c0001t0001g0177 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.703-14C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388082 | ||||||
chr16:4388121
|
C | T | 8 | a0001c0002t0001g0145a0001c0002t0001g0146a0001c0002t0001g0147others(5): Show | 8 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.703-53G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388121 | ||||||
chr16:4388127
|
G | C | 1 | a0002c0001t0001g0163 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.703-59C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388127 | ||||||
chr16:4388199
|
G | A | 40 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(37): Show | 43 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.703-131C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388199 | ||||||
chr16:4388201
|
G | A | 5 | a0001c0002t0002g0267a0003c0003t0001g0266a0003c0003t0001g0268others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-133C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388201 | ||||||
chr16:4388290
|
C | T | 1 | a0001c0004t0001g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.703-222G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388290 | ||||||
chr16:4388459
|
C | G | 3 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0014t0001g0026 | 3 | HG01891.hp1 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.702+86G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388459 | ||||||
chr16:4388460
|
G | T | 3 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0014t0001g0026 | 3 | HG01891.hp1 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.702+85C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 8/27 | chr16 | 4388460 | ||||||
chr16:4388785
|
G | A | 1 | a0001c0002t0001g0104 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.616-154C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4388785 | ||||||
chr16:4388793
|
G | C | 4 | a0002c0001t0001g0184a0002c0001t0001g0185a0002c0001t0001g0228others(1): Show | 4 | NA18969.hp2 NA18977.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-162C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4388793 | ||||||
chr16:4388827
|
G | A | 2 | a0001c0002t0001g0105a0001c0002t0001g0111 | 2 | NA18948.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.616-196C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4388827 | ||||||
chr16:4388948
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.616-317G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4388948 | ||||||
chr16:4388949
|
G | A | 1 | a0003c0003t0001g0268 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.616-318C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4388949 | ||||||
chr16:4389010
|
C | T | 1 | a0001c0002t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.616-379G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389010 | ||||||
chr16:4389028
|
C | A | 1 | a0001c0002t0001g0021 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.616-397G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389028 | ||||||
chr16:4389057
|
G | A | 1 | a0002c0001t0001g0221 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.616-426C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389057 | ||||||
chr16:4389130
|
C | T | 184 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(181): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.616-499G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389130 | ||||||
chr16:4389208
|
G | A | 133 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(130): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.616-577C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389208 | ||||||
chr16:4389542
|
G | A | 5 | a0004c0005t0001g0256a0004c0005t0001g0257a0004c0005t0001g0258others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.616-911C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389542 | ||||||
chr16:4389677
|
G | T | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.616-1046C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389677 | ||||||
chr16:4389760
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.616-1129G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389760 | ||||||
chr16:4389772
|
C | G | 2 | a0002c0001t0001g0164a0002c0001t0001g0165 | 2 | HG01106.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.616-1141G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389772 | ||||||
chr16:4389957
|
G | T | 2 | a0001c0002t0001g0076a0001c0002t0002g0075 | 2 | HG01515.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.616-1326C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4389957 | ||||||
chr16:4390054
|
A | C | 1 | a0001c0002t0001g0051 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.616-1423T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390054 | ||||||
chr16:4390071
|
T | C | 13 | a0002c0001t0001g0009a0002c0001t0001g0061a0002c0001t0001g0063others(10): Show | 14 | HG00423.hp2 HG00597.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.616-1440A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390071 | ||||||
chr16:4390284
|
A | G | 2 | a0001c0002t0001g0052a0001c0002t0001g0053 | 2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.616-1653T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390284 | ||||||
chr16:4390396
|
G | C | 132 | a0001c0002t0001g0049a0001c0002t0001g0145a0001c0002t0001g0146others(129): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.616-1765C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390396 | ||||||
chr16:4390425
|
C | G | 189 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(186): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.616-1794G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390425 | ||||||
chr16:4390526
|
A | G | 12 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(9): Show | 13 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.616-1895T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390526 | ||||||
chr16:4390592
|
C | T | 188 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(185): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.616-1961G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390592 | ||||||
chr16:4390670
|
A | C | 1 | a0002c0001t0001g0063 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.616-2039T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390670 | ||||||
chr16:4390744
|
C | G | 52 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(49): Show | 57 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.616-2113G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390744 | ||||||
chr16:4390810
|
C | T | 2 | a0001c0002t0001g0275a0001c0002t0002g0074 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.616-2179G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390810 | ||||||
chr16:4390827
|
G | A | 6 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(3): Show | 8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.616-2196C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4390827 | ||||||
chr16:4391031
|
T | G | 12 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(9): Show | 13 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.616-2400A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391031 | ||||||
chr16:4391081
|
C | T | 14 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(11): Show | 16 | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(13): Show |
intron_variant | MODIFIER | c.616-2450G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391081 | ||||||
chr16:4391143
|
G | C | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.616-2512C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391143 | ||||||
chr16:4391201
|
C | T | 1 | a0003c0003t0001g0270 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.616-2570G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391201 | ||||||
chr16:4391507
|
G | C | 1 | a0001c0002t0001g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.616-2876C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391507 | ||||||
chr16:4391616
|
A | C | 157 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(154): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.616-2985T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391616 | ||||||
chr16:4391680
|
G | A | 1 | a0010c0012t0001g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.616-3049C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391680 | ||||||
chr16:4391710
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.616-3079C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391710 | ||||||
chr16:4391769
|
C | A | 1 | a0013c0009t0001g0247 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.616-3138G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391769 | ||||||
chr16:4391916
|
A | G | 1 | a0001c0002t0002g0072 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.616-3285T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391916 | ||||||
chr16:4391937
|
G | A | 2 | a0001c0002t0001g0051a0001c0004t0001g0244 | 2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.616-3306C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391937 | ||||||
chr16:4391963
|
C | A | 5 | a0004c0005t0001g0256a0004c0005t0001g0257a0004c0005t0001g0258others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+3326G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4391963 | ||||||
chr16:4392117
|
C | A | 1 | a0002c0001t0001g0018 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.615+3172G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392117 | ||||||
chr16:4392147
|
G | A | 14 | a0001c0002t0002g0267a0003c0003t0001g0014a0003c0003t0001g0264others(11): Show | 15 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.615+3142C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392147 | ||||||
chr16:4392260
|
G | A | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.615+3029C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392260 | ||||||
chr16:4392526
|
C | T | 124 | a0001c0002t0001g0201a0002c0001t0001g0004a0002c0001t0001g0009others(121): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.615+2763G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392526 | ||||||
chr16:4392625
|
C | T | 1 | a0001c0002t0001g0096 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.615+2664G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392625 | ||||||
chr16:4392710
|
C | T | 1 | a0002c0001t0001g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.615+2579G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392710 | ||||||
chr16:4392950
|
A | G | 3 | a0001c0002t0001g0051a0001c0004t0001g0244a0015c0021t0001g0032 | 3 | HG01099.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.615+2339T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392950 | ||||||
chr16:4392974
|
C | T | 1 | a0015c0021t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.615+2315G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4392974 | ||||||
chr16:4393050
|
A | C | 1 | a0009c0008t0002g0059 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.615+2239T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393050 | ||||||
chr16:4393058
|
G | A | 3 | a0001c0002t0001g0051a0001c0004t0001g0244a0015c0021t0001g0032 | 3 | HG01099.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.615+2231C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393058 | ||||||
chr16:4393064
|
G | C | 1 | a0002c0001t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.615+2225C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393064 | ||||||
chr16:4393164
|
C | A | 7 | a0001c0002t0001g0145a0001c0002t0001g0146a0001c0002t0001g0147others(4): Show | 7 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.615+2125G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393164 | ||||||
chr16:4393168
|
A | G | 1 | a0001c0002t0001g0108 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.615+2121T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393168 | ||||||
chr16:4393249
|
T | C | 189 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(186): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.615+2040A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393249 | ||||||
chr16:4393372
|
T | C | 2 | a0001c0002t0001g0051a0001c0004t0001g0244 | 2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.615+1917A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393372 | ||||||
chr16:4393491
|
G | C | 4 | a0002c0001t0001g0184a0002c0001t0001g0185a0002c0001t0001g0228others(1): Show | 4 | NA18969.hp2 NA18977.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.615+1798C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393491 | ||||||
chr16:4393541
|
C | T | 38 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(35): Show | 41 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.615+1748G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393541 | ||||||
chr16:4393567
|
C | A | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.615+1722G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393567 | ||||||
chr16:4393626
|
T | A | 2 | a0001c0002t0001g0051a0001c0004t0001g0244 | 2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.615+1663A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393626 | ||||||
chr16:4393829
|
G | A | 1 | a0002c0001t0001g0235 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.615+1460C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393829 | ||||||
chr16:4393915
|
A | G | 1 | a0001c0002t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.615+1374T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393915 | ||||||
chr16:4393925
|
C | A | 1 | a0001c0002t0001g0028 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.615+1364G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393925 | ||||||
chr16:4393928
|
G | A | 14 | a0001c0002t0002g0267a0003c0003t0001g0014a0003c0003t0001g0264others(11): Show | 15 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.615+1361C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393928 | ||||||
chr16:4393966
|
T | C | 5 | a0001c0002t0002g0002a0001c0002t0002g0085a0001c0002t0002g0245others(2): Show | 7 | HG02109.hp1 HG02145.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.615+1323A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4393966 | ||||||
chr16:4394032
|
C | T | 2 | a0001c0002t0001g0145a0001c0002t0001g0148 | 2 | HG01074.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.615+1257G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394032 | ||||||
chr16:4394043
|
G | T | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.615+1246C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394043 | ||||||
chr16:4394134
|
C | T | 1 | a0001c0002t0002g0002 | 3 | HG02109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.615+1155G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394134 | ||||||
chr16:4394155
|
C | T | 1 | a0002c0001t0001g0018 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.615+1134G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394155 | ||||||
chr16:4394217
|
G | A | 20 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(17): Show | 22 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.615+1072C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394217 | ||||||
chr16:4394238
|
G | A | 5 | a0004c0005t0001g0256a0004c0005t0001g0257a0004c0005t0001g0258others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+1051C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394238 | ||||||
chr16:4394242
|
G | A | 8 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0004t0001g0001others(5): Show | 10 | HG02280.hp1 HG02486.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.615+1047C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394242 | ||||||
chr16:4394247
|
C | T | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.615+1042G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394247 | ||||||
chr16:4394317
|
C | T | 1 | a0001c0002t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.615+972G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394317 | ||||||
chr16:4394318
|
G | A | 1 | a0001c0002t0002g0067 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.615+971C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394318 | ||||||
chr16:4394380
|
C | T | 5 | a0004c0005t0001g0256a0004c0005t0001g0257a0004c0005t0001g0258others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+909G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394380 | ||||||
chr16:4394435
|
C | T | 3 | a0001c0002t0001g0073a0001c0002t0002g0050a0001c0002t0002g0072 | 3 | NA18944.hp2 NA18998.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.615+854G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394435 | ||||||
chr16:4394448
|
C | CA | 25 | a0001c0002t0001g0093a0001c0002t0001g0106a0001c0002t0001g0107others(22): Show | 26 | HG00597.hp2 HG00735.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.615+840dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394448 | ||||||
chr16:4394448
|
CA | C | 8 | a0001c0002t0002g0122a0002c0001t0001g0071a0002c0001t0001g0149others(5): Show | 8 | HG02630.hp2 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.615+840delT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394448 | ||||||
chr16:4394465
|
A | C | 5 | a0003c0003t0001g0014a0003c0003t0001g0270a0003c0003t0001g0271others(2): Show | 6 | HG02451.hp1 HG02559.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+824T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4394465 | ||||||
chr16:4395024
|
T | C | 1 | a0001c0002t0001g0052 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.615+265A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4395024 | ||||||
chr16:4395218
|
C | T | 1 | a0001c0002t0002g0006 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.615+71G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 7/27 | chr16 | 4395218 | ||||||
chr16:4395452
|
C | T | 2 | a0001c0002t0002g0054a0001c0002t0002g0055 | 2 | HG01934.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.565-113G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395452 | ||||||
chr16:4395477
|
G | C | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.565-138C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395477 | ||||||
chr16:4395485
|
C | T | 1 | a0001c0002t0001g0086 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565-146G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395485 | ||||||
chr16:4395587
|
T | C | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565-248A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395587 | ||||||
chr16:4395795
|
C | T | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.565-456G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395795 | ||||||
chr16:4395908
|
A | C | 1 | a0015c0021t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.565-569T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395908 | ||||||
chr16:4395927
|
C | T | 1 | a0001c0002t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.565-588G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395927 | ||||||
chr16:4395975
|
A | ATGTG | 189 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(186): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.565-640_565-637dup others(4): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395975 | ||||||
chr16:4395995
|
G | A | 3 | a0002c0001t0001g0009a0002c0001t0001g0140a0002c0001t0001g0214 | 4 | HG00423.hp2 NA18998.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-656C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395995 | ||||||
chr16:4395996
|
T | TGTGTG | 8 | a0001c0002t0001g0131a0001c0002t0001g0138a0001c0004t0001g0008others(5): Show | 9 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.565-658_565-657ins others(5): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | ||||||
chr16:4395996
|
T | TGTGTGTG others(2): Show |
16 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(13): Show | 17 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.565-658_565-657ins others(9): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | ||||||
chr16:4395996
|
T | TGTGTGTG others(4): Show |
10 | a0001c0002t0001g0039a0001c0004t0001g0001a0001c0004t0001g0041others(7): Show | 12 | HG01099.hp1 HG01243.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.565-658_565-657ins others(11): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | ||||||
chr16:4395996
|
T | TGTGTGTG others(6): Show |
139 | a0001c0002t0001g0019a0001c0002t0001g0034a0001c0002t0001g0038others(136): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.565-658_565-657ins others(13): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | ||||||
chr16:4395996
|
T | TGTGTGTG others(8): Show |
13 | a0002c0001t0001g0069a0002c0001t0001g0119a0002c0001t0001g0120others(10): Show | 13 | HG01258.hp2 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.565-658_565-657ins others(15): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | ||||||
chr16:4395996
|
T | TGTGTGTG others(10): Show |
1 | a0004c0005t0002g0260 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.565-658_565-657ins others(17): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | ||||||
chr16:4395996
|
T | TGTGTGTG others(14): Show |
1 | a0002c0001t0001g0216 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.565-658_565-657ins others(21): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | ||||||
chr16:4395996
|
T | TGTGTGTG others(16): Show |
1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565-658_565-657ins others(23): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4395996 | ||||||
chr16:4396011
|
T | TAC | 7 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(4): Show | 9 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.565-674_565-673dup others(2): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396011 | ||||||
chr16:4396225
|
G | T | 1 | a0001c0002t0002g0245 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.565-886C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396225 | ||||||
chr16:4396468
|
T | G | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565-1129A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396468 | ||||||
chr16:4396552
|
G | A | 7 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(4): Show | 9 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.565-1213C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396552 | ||||||
chr16:4396634
|
C | T | 1 | a0001c0002t0001g0111 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.565-1295G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396634 | ||||||
chr16:4396775
|
C | T | 1 | a0001c0002t0002g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565-1436G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396775 | ||||||
chr16:4396894
|
T | A | 12 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(9): Show | 13 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.565-1555A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396894 | ||||||
chr16:4396915
|
C | T | 1 | a0001c0002t0001g0250 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.565-1576G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4396915 | ||||||
chr16:4397015
|
C | CA | 24 | a0001c0002t0001g0051a0001c0002t0001g0109a0001c0002t0002g0003others(21): Show | 27 | HG00642.hp2 HG01074.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.565-1677dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397015 | ||||||
chr16:4397030
|
AG | A | 7 | a0001c0002t0001g0022a0001c0004t0001g0041a0002c0001t0001g0139others(4): Show | 7 | HG01069.hp2 HG01070.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.565-1692delC | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397030 | ||||||
chr16:4397031
|
G | A | 180 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(177): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.565-1692C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397031 | ||||||
chr16:4397215
|
G | A | 17 | a0001c0002t0002g0267a0003c0003t0001g0014a0003c0003t0001g0261others(14): Show | 18 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.565-1876C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397215 | ||||||
chr16:4397300
|
G | A | 1 | a0015c0021t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.565-1961C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397300 | ||||||
chr16:4397336
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565-1997C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397336 | ||||||
chr16:4397476
|
G | A | 189 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(186): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.565-2137C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397476 | ||||||
chr16:4397551
|
C | A | 191 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(188): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.565-2212G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397551 | ||||||
chr16:4397567
|
C | T | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565-2228G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397567 | ||||||
chr16:4397578
|
C | T | 4 | a0001c0002t0001g0051a0001c0004t0001g0244a0012c0010t0001g0181others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-2239G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397578 | ||||||
chr16:4397582
|
A | G | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565-2243T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397582 | ||||||
chr16:4397677
|
G | A | 17 | a0001c0002t0002g0267a0003c0003t0001g0014a0003c0003t0001g0261others(14): Show | 18 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.565-2338C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397677 | ||||||
chr16:4397683
|
G | A | 1 | a0001c0002t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.565-2344C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397683 | ||||||
chr16:4397738
|
C | A | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565-2399G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397738 | ||||||
chr16:4397770
|
C | T | 138 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(135): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.565-2431G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397770 | ||||||
chr16:4397939
|
CAG | C | 3 | a0001c0002t0001g0051a0001c0004t0001g0244a0015c0021t0001g0032 | 3 | HG01099.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.565-2602_565-2601d others(4): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397939 | ||||||
chr16:4397947
|
C | T | 1 | a0001c0002t0002g0050 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.565-2608G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397947 | ||||||
chr16:4397956
|
G | A | 4 | a0002c0001t0001g0156a0002c0001t0001g0204a0002c0001t0001g0208others(1): Show | 4 | HG01258.hp2 HG01346.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-2617C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397956 | ||||||
chr16:4397969
|
C | T | 278 | a0001c0002t0001g0005a0001c0002t0001g0007a0001c0002t0001g0019others(275): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.565-2630G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397969 | ||||||
chr16:4397985
|
C | T | 1 | a0002c0001t0001g0222 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.565-2646G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4397985 | ||||||
chr16:4398074
|
C | T | 1 | a0001c0002t0002g0072 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.565-2735G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398074 | ||||||
chr16:4398247
|
T | C | 1 | a0002c0001t0001g0232 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.565-2908A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398247 | ||||||
chr16:4398266
|
T | A | 1 | a0002c0001t0001g0205 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.565-2927A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398266 | ||||||
chr16:4398389
|
C | T | 3 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0014t0001g0026 | 3 | HG01891.hp1 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.565-3050G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398389 | ||||||
chr16:4398436
|
G | C | 1 | a0002c0001t0001g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.565-3097C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398436 | ||||||
chr16:4398495
|
G | A | 31 | a0001c0002t0001g0007a0001c0002t0001g0049a0001c0002t0001g0057others(28): Show | 34 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.565-3156C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398495 | ||||||
chr16:4398526
|
C | T | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565-3187G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398526 | ||||||
chr16:4398561
|
G | A | 7 | a0001c0002t0001g0131a0001c0002t0001g0138a0001c0004t0001g0008others(4): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.565-3222C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398561 | ||||||
chr16:4398652
|
C | T | 37 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(34): Show | 40 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.565-3313G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398652 | ||||||
chr16:4398665
|
G | GA | 6 | a0001c0002t0001g0057a0001c0002t0001g0093a0001c0002t0001g0108others(3): Show | 6 | HG00544.hp2 HG00741.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.565-3327dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398665 | ||||||
chr16:4398665
|
GA | G | 7 | a0001c0002t0001g0034a0001c0002t0002g0062a0001c0004t0001g0137others(4): Show | 7 | HG00673.hp2 HG01891.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.565-3327delT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398665 | ||||||
chr16:4398697
|
T | TGGTGGCT others(136): Show |
1 | a0015c0021t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.565-3359_565-3358i others(145): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398697 | ||||||
chr16:4398727
|
G | T | 4 | a0001c0002t0001g0051a0001c0004t0001g0244a0008c0024t0005g0279others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-3388C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398727 | ||||||
chr16:4398925
|
A | G | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565-3586T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398925 | ||||||
chr16:4398967
|
C | CA | 13 | a0001c0002t0001g0034a0001c0002t0001g0051a0001c0002t0002g0047others(10): Show | 13 | HG01934.hp2 HG02615.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.565-3629dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4398967 | ||||||
chr16:4399021
|
C | T | 1 | a0002c0001t0001g0178 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.565-3682G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399021 | ||||||
chr16:4399132
|
C | T | 1 | a0018c0016t0003g0259 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.565-3793G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399132 | ||||||
chr16:4399321
|
G | A | 5 | a0001c0002t0002g0116a0004c0005t0001g0256a0004c0005t0001g0257others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-3982C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399321 | ||||||
chr16:4399489
|
C | T | 2 | a0001c0002t0002g0112a0001c0002t0002g0116 | 2 | NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.565-4150G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399489 | ||||||
chr16:4399723
|
G | A | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565-4384C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399723 | ||||||
chr16:4399884
|
C | A | 1 | a0001c0002t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.565-4545G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399884 | ||||||
chr16:4399902
|
G | T | 2 | a0004c0005t0002g0260a0018c0016t0003g0259 | 2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.565-4563C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4399902 | ||||||
chr16:4400008
|
C | T | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565-4669G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400008 | ||||||
chr16:4400033
|
C | T | 1 | a0001c0002t0001g0250 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.565-4694G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400033 | ||||||
chr16:4400145
|
C | T | 1 | a0002c0001t0001g0232 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.565-4806G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400145 | ||||||
chr16:4400420
|
T | G | 181 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(178): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.564+5071A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400420 | ||||||
chr16:4400519
|
G | A | 38 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(35): Show | 41 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.564+4972C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400519 | ||||||
chr16:4400632
|
TCAAAAAC others(5): Show |
T | 1 | a0001c0002t0002g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.564+4847_564+4858d others(14): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400632 | ||||||
chr16:4400665
|
C | CA | 40 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(37): Show | 43 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.564+4825dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400665 | ||||||
chr16:4400679
|
G | C | 2 | a0001c0002t0001g0109a0001c0002t0002g0003 | 4 | HG01074.hp1 HG01109.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+4812C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400679 | ||||||
chr16:4400757
|
T | C | 2 | a0001c0002t0001g0034a0001c0002t0001g0051 | 2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.564+4734A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400757 | ||||||
chr16:4400797
|
C | CAAT | 25 | a0001c0002t0001g0027a0001c0002t0001g0030a0001c0002t0002g0047others(22): Show | 25 | HG00423.hp2 HG01516.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.564+4691_564+4693d others(5): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400797 | ||||||
chr16:4400797
|
C | CAATAAT | 25 | a0001c0002t0001g0146a0001c0002t0001g0147a0001c0002t0001g0152others(22): Show | 25 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.564+4688_564+4693d others(8): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400797 | ||||||
chr16:4400797
|
C | CAATAATA others(2): Show |
96 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0038others(93): Show | 105 | HG00280.hp1 HG00597.hp1 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.564+4685_564+4693d others(11): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400797 | ||||||
chr16:4400797
|
C | CAATAATA others(5): Show |
34 | a0001c0002t0001g0022a0001c0002t0001g0023a0001c0002t0001g0024others(31): Show | 36 | HG00280.hp2 HG00544.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.564+4682_564+4693d others(14): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400797 | ||||||
chr16:4400797
|
C | CAATAATA others(8): Show |
8 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0028others(5): Show | 9 | HG00642.hp1 HG01074.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.564+4679_564+4693d others(17): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400797 | ||||||
chr16:4400797
|
C | CAATAATA others(11): Show |
2 | a0003c0003t0001g0264a0003c0003t0001g0265 | 2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.564+4676_564+4693d others(20): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400797 | ||||||
chr16:4400999
|
C | T | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+4492G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4400999 | ||||||
chr16:4401023
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.564+4468G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401023 | ||||||
chr16:4401026
|
A | C | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+4465T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401026 | ||||||
chr16:4401039
|
T | G | 1 | a0002c0001t0001g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.564+4452A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401039 | ||||||
chr16:4401079
|
G | A | 1 | a0001c0002t0002g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.564+4412C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401079 | ||||||
chr16:4401140
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.564+4351G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401140 | ||||||
chr16:4401154
|
T | C | 1 | a0001c0002t0001g0019 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.564+4337A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401154 | ||||||
chr16:4401228
|
G | A | 1 | a0002c0001t0001g0110 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.564+4263C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401228 | ||||||
chr16:4401298
|
G | A | 2 | a0001c0002t0001g0034a0001c0002t0001g0051 | 2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.564+4193C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401298 | ||||||
chr16:4401319
|
C | T | 1 | a0001c0002t0001g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.564+4172G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401319 | ||||||
chr16:4401337
|
T | C | 1 | a0001c0002t0001g0111 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.564+4154A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401337 | ||||||
chr16:4401664
|
C | T | 2 | a0002c0001t0001g0178a0008c0024t0005g0279 | 2 | HG02922.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.564+3827G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401664 | ||||||
chr16:4401734
|
G | C | 1 | a0001c0002t0002g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.564+3757C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401734 | ||||||
chr16:4401911
|
C | CT | 44 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(41): Show | 48 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.564+3579dupA | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4401911 | ||||||
chr16:4402063
|
C | T | 1 | a0007c0025t0001g0243 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.564+3428G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402063 | ||||||
chr16:4402140
|
T | C | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.564+3351A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402140 | ||||||
chr16:4402241
|
TTTGTTGT others(2): Show |
T | 23 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(20): Show | 25 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.564+3241_564+3249d others(11): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402241 | ||||||
chr16:4402256
|
G | C | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+3235C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402256 | ||||||
chr16:4402265
|
G | T | 1 | a0019c0015t0001g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.564+3226C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402265 | ||||||
chr16:4402321
|
T | C | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.564+3170A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402321 | ||||||
chr16:4402327
|
C | T | 1 | a0001c0002t0001g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.564+3164G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402327 | ||||||
chr16:4402392
|
G | A | 1 | a0001c0002t0001g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.564+3099C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402392 | ||||||
chr16:4402482
|
A | T | 1 | a0001c0002t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.564+3009T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402482 | ||||||
chr16:4402528
|
T | A | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+2963A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402528 | ||||||
chr16:4402583
|
G | A | 89 | a0001c0002t0001g0201a0001c0002t0001g0203a0002c0001t0001g0004others(86): Show | 95 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.564+2908C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402583 | ||||||
chr16:4402598
|
G | C | 2 | a0001c0002t0001g0151a0001c0002t0001g0152 | 2 | HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.564+2893C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402598 | ||||||
chr16:4402757
|
G | A | 1 | a0002c0001t0001g0211 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.564+2734C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402757 | ||||||
chr16:4402790
|
C | T | 7 | a0002c0001t0001g0162a0002c0001t0001g0163a0002c0001t0001g0164others(4): Show | 7 | HG01106.hp2 HG01168.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.564+2701G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402790 | ||||||
chr16:4402835
|
G | A | 2 | a0002c0001t0001g0212a0002c0001t0001g0252 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.564+2656C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402835 | ||||||
chr16:4402865
|
T | A | 1 | a0015c0021t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.564+2626A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4402865 | ||||||
chr16:4403000
|
T | C | 1 | a0001c0002t0002g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.564+2491A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403000 | ||||||
chr16:4403065
|
C | A | 6 | a0001c0002t0001g0088a0001c0002t0001g0090a0001c0002t0001g0130others(3): Show | 6 | HG02055.hp1 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+2426G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403065 | ||||||
chr16:4403087
|
C | T | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.564+2404G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403087 | ||||||
chr16:4403096
|
T | C | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.564+2395A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403096 | ||||||
chr16:4403253
|
C | T | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+2238G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403253 | ||||||
chr16:4403278
|
G | A | 1 | a0002c0001t0001g0213 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.564+2213C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403278 | ||||||
chr16:4403285
|
T | A | 2 | a0001c0002t0001g0022a0001c0002t0001g0023 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.564+2206A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403285 | ||||||
chr16:4403308
|
G | A | 1 | a0001c0002t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.564+2183C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403308 | ||||||
chr16:4403318
|
C | G | 100 | a0001c0002t0001g0057a0001c0002t0001g0169a0001c0002t0001g0201others(97): Show | 107 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.564+2173G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403318 | ||||||
chr16:4403351
|
G | C | 133 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(130): Show | 142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.564+2140C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403351 | ||||||
chr16:4403363
|
C | T | 2 | a0001c0002t0001g0093a0001c0002t0002g0092 | 2 | HG01255.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.564+2128G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403363 | ||||||
chr16:4403436
|
C | G | 5 | a0004c0005t0001g0256a0004c0005t0001g0257a0004c0005t0001g0258others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+2055G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403436 | ||||||
chr16:4403526
|
G | C | 1 | a0015c0021t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.564+1965C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403526 | ||||||
chr16:4403595
|
G | C | 1 | a0002c0001t0001g0214 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.564+1896C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403595 | ||||||
chr16:4403713
|
T | C | 11 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(8): Show | 11 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+1778A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403713 | ||||||
chr16:4403715
|
G | A | 14 | a0001c0002t0002g0267a0003c0003t0001g0014a0003c0003t0001g0264others(11): Show | 15 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.564+1776C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403715 | ||||||
chr16:4403805
|
G | C | 1 | a0001c0002t0002g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.564+1686C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403805 | ||||||
chr16:4403941
|
G | A | 15 | a0002c0001t0001g0215a0002c0001t0001g0216a0002c0001t0001g0217others(12): Show | 15 | HG00544.hp2 HG02040.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.564+1550C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4403941 | ||||||
chr16:4404135
|
A | G | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.564+1356T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404135 | ||||||
chr16:4404167
|
G | A | 1 | a0002c0001t0001g0141 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.564+1324C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404167 | ||||||
chr16:4404169
|
A | G | 179 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(176): Show | 191 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.564+1322T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404169 | ||||||
chr16:4404443
|
C | A | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+1048G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404443 | ||||||
chr16:4404758
|
C | T | 2 | a0004c0005t0001g0256a0004c0005t0001g0258 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.564+733G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404758 | ||||||
chr16:4404813
|
G | A | 1 | a0002c0001t0001g0223 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.564+678C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404813 | ||||||
chr16:4404911
|
T | G | 1 | a0001c0002t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.564+580A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4404911 | ||||||
chr16:4405049
|
A | T | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+442T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4405049 | ||||||
chr16:4405107
|
G | A | 37 | a0001c0002t0001g0007a0001c0002t0001g0049a0001c0002t0001g0057others(34): Show | 40 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.564+384C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4405107 | ||||||
chr16:4405425
|
C | A | 1 | a0002c0001t0001g0224 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.564+66G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4405425 | ||||||
chr16:4405435
|
C | T | 5 | a0001c0002t0001g0145a0001c0002t0001g0146a0001c0002t0001g0147others(2): Show | 5 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+56G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4405435 | ||||||
chr16:4405444
|
G | A | 1 | a0001c0002t0002g0112 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.564+47C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 6/27 | chr16 | 4405444 | ||||||
chr16:4405596
|
C | T | 6 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(3): Show | 7 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.488-29G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405596 | ||||||
chr16:4405625
|
G | T | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.488-58C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405625 | ||||||
chr16:4405646
|
G | A | 2 | a0001c0002t0001g0034a0001c0002t0001g0051 | 2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.488-79C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405646 | ||||||
chr16:4405673
|
C | A | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.488-106G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405673 | ||||||
chr16:4405674
|
G | A | 178 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(175): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.488-107C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405674 | ||||||
chr16:4405777
|
ATCACTCA others(24): Show |
A | 3 | a0002c0001t0001g0012a0002c0001t0001g0226a0011c0011t0001g0225 | 4 | HG00280.hp2 HG02738.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-241_488-211del others(31): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405777 | ||||||
chr16:4405809
|
C | A | 3 | a0002c0001t0001g0012a0002c0001t0001g0226a0011c0011t0001g0225 | 4 | HG00280.hp2 HG02738.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-242G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405809 | ||||||
chr16:4405812
|
GCCT | G | 3 | a0002c0001t0001g0012a0002c0001t0001g0226a0011c0011t0001g0225 | 4 | HG00280.hp2 HG02738.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-248_488-246del others(3): Show |
CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405812 | ||||||
chr16:4405816
|
G | T | 3 | a0002c0001t0001g0012a0002c0001t0001g0226a0011c0011t0001g0225 | 4 | HG00280.hp2 HG02738.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-249C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405816 | ||||||
chr16:4405819
|
T | C | 3 | a0002c0001t0001g0012a0002c0001t0001g0226a0011c0011t0001g0225 | 4 | HG00280.hp2 HG02738.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-252A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405819 | ||||||
chr16:4405820
|
C | A | 3 | a0002c0001t0001g0012a0002c0001t0001g0226a0011c0011t0001g0225 | 4 | HG00280.hp2 HG02738.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-253G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4405820 | ||||||
chr16:4406085
|
C | T | 1 | a0001c0002t0001g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.488-518G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406085 | ||||||
chr16:4406116
|
C | T | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.488-549G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406116 | ||||||
chr16:4406117
|
G | A | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.488-550C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406117 | ||||||
chr16:4406188
|
C | T | 1 | a0001c0002t0001g0057 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.488-621G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406188 | ||||||
chr16:4406189
|
G | A | 20 | a0001c0002t0001g0275a0001c0002t0002g0267a0003c0003t0001g0014others(17): Show | 21 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.488-622C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406189 | ||||||
chr16:4406320
|
G | A | 1 | a0001c0002t0001g0113 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.488-753C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406320 | ||||||
chr16:4406328
|
C | T | 1 | a0002c0001t0001g0160 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.488-761G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406328 | ||||||
chr16:4406552
|
G | T | 4 | a0004c0005t0001g0256a0004c0005t0001g0258a0004c0005t0002g0260others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+949C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406552 | ||||||
chr16:4406651
|
A | T | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.487+850T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406651 | ||||||
chr16:4406689
|
C | T | 1 | a0001c0014t0001g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.487+812G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406689 | ||||||
chr16:4406700
|
C | T | 2 | a0001c0002t0002g0047a0001c0002t0002g0251 | 2 | NA18977.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.487+801G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406700 | ||||||
chr16:4406751
|
T | C | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.487+750A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406751 | ||||||
chr16:4406830
|
G | A | 6 | a0001c0004t0001g0008a0001c0004t0001g0133a0001c0004t0001g0134others(3): Show | 7 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.487+671C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406830 | ||||||
chr16:4406831
|
C | T | 12 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(9): Show | 13 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.487+670G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406831 | ||||||
chr16:4406832
|
G | A | 1 | a0002c0001t0001g0227 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.487+669C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406832 | ||||||
chr16:4406923
|
G | A | 1 | a0002c0001t0001g0236 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.487+578C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4406923 | ||||||
chr16:4407016
|
C | T | 23 | a0001c0002t0001g0275a0001c0002t0002g0267a0003c0003t0001g0014others(20): Show | 24 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.487+485G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407016 | ||||||
chr16:4407018
|
G | C | 2 | a0002c0001t0001g0228a0002c0001t0001g0229 | 2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.487+483C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407018 | ||||||
chr16:4407099
|
C | T | 22 | a0001c0002t0002g0267a0003c0003t0001g0014a0003c0003t0001g0261others(19): Show | 23 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.487+402G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407099 | ||||||
chr16:4407101
|
C | T | 12 | a0001c0002t0001g0145a0001c0002t0001g0146a0001c0002t0001g0147others(9): Show | 12 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.487+400G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407101 | ||||||
chr16:4407110
|
G | T | 1 | a0002c0001t0001g0155 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.487+391C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407110 | ||||||
chr16:4407275
|
C | T | 1 | a0006c0026t0001g0129 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.487+226G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407275 | ||||||
chr16:4407277
|
G | GA | 33 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0053others(30): Show | 36 | HG00735.hp2 HG01099.hp1 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.487+223dupT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407277 | ||||||
chr16:4407288
|
A | G | 1 | a0001c0002t0001g0024 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.487+213T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407288 | ||||||
chr16:4407289
|
A | T | 1 | a0001c0002t0001g0024 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.487+212T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407289 | ||||||
chr16:4407291
|
C | A | 1 | a0001c0002t0001g0024 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.487+210G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407291 | ||||||
chr16:4407292
|
A | G | 1 | a0001c0002t0001g0127 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.487+209T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 5/27 | chr16 | 4407292 | ||||||
chr16:4407711
|
A | G | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.304-27T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4407711 | ||||||
chr16:4407743
|
C | G | 1 | a0001c0004t0001g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.304-59G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4407743 | ||||||
chr16:4407744
|
T | G | 1 | a0001c0002t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.304-60A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4407744 | ||||||
chr16:4407772
|
G | A | 3 | a0002c0006t0001g0013a0002c0006t0001g0248a0013c0009t0001g0247 | 4 | HG00733.hp1 HG01106.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-88C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4407772 | ||||||
chr16:4407906
|
C | G | 181 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(178): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.304-222G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4407906 | ||||||
chr16:4407953
|
A | G | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.303+228T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4407953 | ||||||
chr16:4408070
|
G | A | 1 | a0001c0002t0002g0115 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.303+111C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4408070 | ||||||
chr16:4408077
|
T | C | 1 | a0001c0002t0002g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.303+104A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4408077 | ||||||
chr16:4408139
|
G | A | 2 | a0001c0002t0001g0052a0001c0002t0001g0053 | 2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.303+42C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 4/27 | chr16 | 4408139 | ||||||
chr16:4408326
|
C | T | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233-75G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408326 | ||||||
chr16:4408329
|
G | A | 5 | a0004c0005t0001g0256a0004c0005t0001g0257a0004c0005t0001g0258others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-78C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408329 | ||||||
chr16:4408388
|
C | T | 6 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(3): Show | 8 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.233-137G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408388 | ||||||
chr16:4408428
|
T | C | 1 | a0001c0002t0001g0025 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.233-177A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408428 | ||||||
chr16:4408505
|
C | T | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.233-254G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408505 | ||||||
chr16:4408559
|
G | C | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233-308C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408559 | ||||||
chr16:4408590
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233-339C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408590 | ||||||
chr16:4408733
|
T | C | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233-482A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408733 | ||||||
chr16:4408738
|
A | G | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233-487T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4408738 | ||||||
chr16:4409092
|
A | T | 1 | a0001c0002t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.233-841T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409092 | ||||||
chr16:4409108
|
G | A | 1 | a0001c0002t0002g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.233-857C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409108 | ||||||
chr16:4409111
|
G | T | 2 | a0001c0002t0002g0054a0001c0002t0002g0055 | 2 | HG01934.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.233-860C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409111 | ||||||
chr16:4409145
|
G | T | 1 | a0002c0001t0001g0159 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.233-894C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409145 | ||||||
chr16:4409154
|
G | A | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233-903C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409154 | ||||||
chr16:4409161
|
T | A | 2 | a0002c0001t0001g0233a0002c0001t0001g0253 | 2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.233-910A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409161 | ||||||
chr16:4409198
|
G | A | 1 | a0002c0001t0001g0018 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.233-947C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409198 | ||||||
chr16:4409209
|
G | A | 1 | a0001c0002t0001g0051 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.233-958C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409209 | ||||||
chr16:4409242
|
G | A | 1 | a0001c0002t0002g0116 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.233-991C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409242 | ||||||
chr16:4409267
|
C | T | 7 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(4): Show | 8 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-1016G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409267 | ||||||
chr16:4409341
|
T | C | 1 | a0001c0004t0001g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.233-1090A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409341 | ||||||
chr16:4409413
|
G | A | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.233-1162C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409413 | ||||||
chr16:4409434
|
G | A | 1 | a0001c0002t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.233-1183C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409434 | ||||||
chr16:4409496
|
G | A | 14 | a0001c0002t0002g0267a0003c0003t0001g0014a0003c0003t0001g0264others(11): Show | 15 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.233-1245C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409496 | ||||||
chr16:4409589
|
C | T | 1 | a0002c0001t0001g0158 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.233-1338G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409589 | ||||||
chr16:4409613
|
A | G | 1 | a0001c0002t0001g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.233-1362T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409613 | ||||||
chr16:4409664
|
T | A | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.233-1413A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409664 | ||||||
chr16:4409699
|
C | A | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.233-1448G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409699 | ||||||
chr16:4409756
|
T | A | 1 | a0001c0002t0001g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.233-1505A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409756 | ||||||
chr16:4409776
|
G | A | 3 | a0002c0001t0001g0234a0002c0001t0001g0235a0002c0001t0001g0236 | 3 | HG02015.hp1 HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.233-1525C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409776 | ||||||
chr16:4409815
|
G | C | 1 | a0001c0002t0001g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.233-1564C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409815 | ||||||
chr16:4409833
|
A | G | 187 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(184): Show | 199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.233-1582T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409833 | ||||||
chr16:4409904
|
T | G | 1 | a0001c0002t0001g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.233-1653A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4409904 | ||||||
chr16:4410048
|
A | G | 185 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(182): Show | 197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.233-1797T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410048 | ||||||
chr16:4410097
|
G | T | 1 | a0013c0009t0001g0247 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.233-1846C>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410097 | ||||||
chr16:4410113
|
A | G | 187 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(184): Show | 199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.233-1862T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410113 | ||||||
chr16:4410132
|
G | A | 185 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(182): Show | 197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.233-1881C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410132 | ||||||
chr16:4410155
|
T | G | 1 | a0001c0002t0001g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.233-1904A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410155 | ||||||
chr16:4410579
|
T | G | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+1777A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410579 | ||||||
chr16:4410771
|
T | C | 4 | a0002c0001t0001g0157a0002c0001t0001g0237a0002c0001t0001g0238others(1): Show | 4 | NA18942.hp2 NA19000.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+1585A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410771 | ||||||
chr16:4410818
|
T | C | 1 | a0017c0020t0002g0046 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.232+1538A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410818 | ||||||
chr16:4410842
|
T | C | 1 | a0001c0002t0002g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.232+1514A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410842 | ||||||
chr16:4410886
|
T | C | 1 | a0016c0022t0001g0123 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.232+1470A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410886 | ||||||
chr16:4410917
|
G | A | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+1439C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410917 | ||||||
chr16:4410919
|
G | A | 1 | a0002c0001t0001g0249 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.232+1437C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4410919 | ||||||
chr16:4411001
|
G | C | 3 | a0001c0002t0001g0125a0001c0002t0001g0126a0019c0015t0001g0124 | 3 | HG03654.hp1 HG03688.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.232+1355C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411001 | ||||||
chr16:4411018
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.232+1338G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411018 | ||||||
chr16:4411020
|
T | G | 1 | a0001c0002t0001g0127 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.232+1336A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411020 | ||||||
chr16:4411048
|
G | A | 14 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(11): Show | 15 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.232+1308C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411048 | ||||||
chr16:4411088
|
T | C | 1 | a0001c0002t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.232+1268A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411088 | ||||||
chr16:4411132
|
G | C | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+1224C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411132 | ||||||
chr16:4411559
|
A | T | 6 | a0001c0002t0001g0052a0001c0002t0001g0053a0002c0001t0001g0155others(3): Show | 6 | HG01346.hp1 HG01361.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+797T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411559 | ||||||
chr16:4411597
|
G | C | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+759C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411597 | ||||||
chr16:4411650
|
A | G | 5 | a0004c0005t0001g0256a0004c0005t0001g0257a0004c0005t0001g0258others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+706T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411650 | ||||||
chr16:4411683
|
C | T | 2 | a0005c0007t0001g0042a0005c0007t0001g0043 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.232+673G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411683 | ||||||
chr16:4411721
|
C | G | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+635G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411721 | ||||||
chr16:4411860
|
A | G | 182 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(179): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.232+496T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411860 | ||||||
chr16:4411996
|
G | A | 1 | a0001c0002t0001g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.232+360C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411996 | ||||||
chr16:4411997
|
A | G | 1 | a0001c0002t0001g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.232+359T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4411997 | ||||||
chr16:4412025
|
C | G | 1 | a0001c0002t0002g0048 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.232+331G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4412025 | ||||||
chr16:4412033
|
G | A | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232+323C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4412033 | ||||||
chr16:4412053
|
A | C | 1 | a0002c0001t0001g0154 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.232+303T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4412053 | ||||||
chr16:4412066
|
G | A | 4 | a0004c0005t0001g0256a0004c0005t0001g0258a0004c0005t0002g0260others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+290C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 3/27 | chr16 | 4412066 | ||||||
chr16:4412469
|
C | T | 2 | a0001c0002t0002g0047a0001c0002t0002g0251 | 2 | NA18977.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.158-39G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412469 | ||||||
chr16:4412618
|
A | G | 125 | a0001c0002t0001g0145a0001c0002t0001g0146a0001c0002t0001g0147others(122): Show | 132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.158-188T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412618 | ||||||
chr16:4412623
|
T | C | 1 | a0002c0001t0001g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.158-193A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412623 | ||||||
chr16:4412735
|
T | A | 1 | a0002c0001t0001g0242 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.158-305A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412735 | ||||||
chr16:4412795
|
A | G | 2 | a0001c0002t0002g0037a0002c0001t0001g0036 | 2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.158-365T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412795 | ||||||
chr16:4412831
|
C | T | 181 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(178): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.158-401G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412831 | ||||||
chr16:4412835
|
G | A | 124 | a0001c0002t0001g0145a0001c0002t0001g0146a0001c0002t0001g0147others(121): Show | 131 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.158-405C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412835 | ||||||
chr16:4412896
|
C | A | 113 | a0001c0002t0001g0169a0001c0002t0001g0201a0001c0002t0001g0203others(110): Show | 120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.157+412G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412896 | ||||||
chr16:4412926
|
A | T | 1 | a0001c0002t0002g0047 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.157+382T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4412926 | ||||||
chr16:4413045
|
C | T | 1 | a0002c0001t0001g0036 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.157+263G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4413045 | ||||||
chr16:4413217
|
A | G | 2 | a0001c0002t0002g0006a0017c0020t0002g0046 | 3 | HG03209.hp2 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.157+91T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4413217 | ||||||
chr16:4413283
|
A | C | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.157+25T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 2/27 | chr16 | 4413283 | ||||||
chr16:4413425
|
A | C | 1 | a0002c0001t0001g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.61-21T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4413425 | ||||||
chr16:4413763
|
C | G | 2 | a0001c0002t0002g0037a0002c0001t0001g0036 | 2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.61-359G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4413763 | ||||||
chr16:4413767
|
G | A | 1 | a0001c0002t0001g0130 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.61-363C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4413767 | ||||||
chr16:4413845
|
G | A | 157 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(154): Show | 167 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.61-441C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4413845 | ||||||
chr16:4413914
|
G | C | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.61-510C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4413914 | ||||||
chr16:4413999
|
C | T | 1 | a0001c0002t0001g0044 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.61-595G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4413999 | ||||||
chr16:4414014
|
T | C | 180 | a0001c0002t0001g0005a0001c0002t0001g0019a0001c0002t0001g0020others(177): Show | 192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.61-610A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414014 | ||||||
chr16:4414190
|
CA | C | 153 | a0001c0002t0001g0019a0001c0002t0001g0038a0001c0002t0001g0039others(150): Show | 163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.61-787delT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414190 | ||||||
chr16:4414190
|
CAA | C | 7 | a0002c0001t0001g0033a0002c0001t0001g0141a0002c0001t0001g0142others(4): Show | 7 | HG01255.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-788_61-787delTT | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414190 | ||||||
chr16:4414304
|
C | T | 2 | a0002c0001t0001g0009a0002c0001t0001g0140 | 3 | NA18998.hp2 NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.61-900G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414304 | ||||||
chr16:4414372
|
G | A | 1 | a0001c0004t0001g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.61-968C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414372 | ||||||
chr16:4414545
|
A | G | 1 | a0002c0001t0001g0139 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.61-1141T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414545 | ||||||
chr16:4414616
|
T | C | 127 | a0001c0002t0001g0145a0001c0002t0001g0146a0001c0002t0001g0147others(124): Show | 134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.61-1212A>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414616 | ||||||
chr16:4414689
|
A | G | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.61-1285T>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414689 | ||||||
chr16:4414692
|
G | C | 2 | a0001c0002t0002g0245a0001c0002t0002g0246 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.61-1288C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414692 | ||||||
chr16:4414815
|
C | T | 1 | a0002c0001t0001g0033 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.61-1411G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414815 | ||||||
chr16:4414931
|
G | A | 3 | a0002c0006t0001g0013a0002c0006t0001g0248a0013c0009t0001g0247 | 4 | HG00733.hp1 HG01106.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-1527C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414931 | ||||||
chr16:4414955
|
C | G | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.60+1504G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414955 | ||||||
chr16:4414956
|
G | A | 13 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(10): Show | 14 | HG00544.hp2 HG00642.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.60+1503C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4414956 | ||||||
chr16:4415116
|
A | T | 1 | a0015c0021t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.60+1343T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415116 | ||||||
chr16:4415212
|
G | A | 1 | a0001c0002t0001g0250 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.60+1247C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415212 | ||||||
chr16:4415253
|
T | G | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.60+1206A>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415253 | ||||||
chr16:4415329
|
C | T | 4 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0017others(1): Show | 4 | HG02027.hp2 NA18969.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+1130G>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415329 | ||||||
chr16:4415389
|
T | A | 1 | a0001c0002t0002g0251 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.60+1070A>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415389 | ||||||
chr16:4415390
|
A | C | 1 | a0001c0002t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.60+1069T>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415390 | ||||||
chr16:4415692
|
C | A | 1 | a0008c0024t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.60+767G>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415692 | ||||||
chr16:4415713
|
A | T | 12 | a0001c0002t0001g0005a0001c0002t0001g0020a0001c0002t0001g0021others(9): Show | 13 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.60+746T>A | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415713 | ||||||
chr16:4415849
|
C | G | 1 | a0001c0002t0001g0019 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.60+610G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415849 | ||||||
chr16:4415869
|
C | G | 5 | a0004c0005t0001g0256a0004c0005t0001g0257a0004c0005t0001g0258others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.60+590G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415869 | ||||||
chr16:4415962
|
G | A | 1 | a0002c0001t0001g0252 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.60+497C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4415962 | ||||||
chr16:4416185
|
G | A | 1 | a0002c0001t0001g0253 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.60+274C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4416185 | ||||||
chr16:4416235
|
G | C | 2 | a0002c0001t0001g0254a0002c0001t0001g0255 | 2 | NA18982.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.60+224C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4416235 | ||||||
chr16:4416306
|
C | G | 4 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0017others(1): Show | 4 | HG02027.hp2 NA18969.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+153G>C | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4416306 | ||||||
chr16:4416429
|
G | A | 23 | a0001c0002t0001g0275a0001c0002t0002g0267a0003c0003t0001g0014others(20): Show | 24 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.60+30C>T | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4416429 | ||||||
chr16:4416440
|
G | C | 1 | a0002c0001t0002g0278 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.60+19C>G | CORO7 | ENSG00000262246.6 | transcript | ENST00000251166.9 | protein_coding | 1/27 | chr16 | 4416440 |