geneid | 81831 |
---|---|
ensemblid | ENSG00000171208.10 |
hgncid | 14644 |
symbol | NETO2 |
name | neuropilin and tolloid like 2 |
refseq_nuc | NM_018092.5 |
refseq_prot | NP_060562.3 |
ensembl_nuc | ENST00000562435.6 |
ensembl_prot | ENSP00000455169.1 |
mane_status | MANE Select |
chr | chr16 |
start | 47077703 |
end | 47143945 |
strand | - |
ver | v1.2 |
region | chr16:47077703-47143945 |
region5000 | chr16:47072703-47148945 |
regionname0 | NETO2_chr16_47077703_47143945 |
regionname5000 | NETO2_chr16_47072703_47148945 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 525 | 160 | 75 | 30 | 27 | 6 | 20 | 16 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0002 | 0/0 | 525 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0003 | 0/0 | 525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1578 | 160 | 75 | 30 | 27 | 6 | 20 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
c0002 | 0/0 | 1578 | 7 | 7 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
c0003 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5852 | 88 | 26 | 19 | 26 | 5 | 12 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0002 | 0/0 | 5857 | 22 | 18 | 4 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0003 | 0/0 | 5857 | 8 | 8 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0004 | 0/0 | 5857 | 5 | 5 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0005 | 0/0 | 5857 | 4 | 4 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0006 | 0/0 | 5857 | 4 | 4 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0007 | 0/0 | 5857 | 4 | 4 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0008 | 0/1 | 5852 | 3 | 0 | 2 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0009 | 0/0 | 5852 | 3 | 0 | 0 | 0 | 0 | 3 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0010 | 0/0 | 5852 | 3 | 0 | 0 | 0 | 0 | 3 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0011 | 0/0 | 5857 | 3 | 3 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0012 | 0/0 | 5848 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0013 | 0/0 | 5852 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0014 | 0/0 | 5857 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0015 | 0/0 | 5852 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0016 | 0/0 | 5852 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0017 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0018 | 0/0 | 5852 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0019 | 0/0 | 5852 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0020 | 0/0 | 5852 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0021 | 1/0 | 5852 | 1 | 0 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0022 | 0/0 | 5852 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0023 | 0/0 | 5852 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0024 | 0/0 | 5857 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0025 | 0/0 | 5857 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0026 | 0/0 | 5857 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0027 | 0/0 | 5852 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0028 | 0/0 | 5852 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
t0029 | 0/0 | 5852 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0003 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0012 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1578 | 160 | 75 | 30 | 27 | 6 | 20 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0002c0002 | 0/0 | 1578 | 7 | 7 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0003c0003 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7429 | 87 | 26 | 19 | 25 | 5 | 12 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0002 | 0/0 | 7434 | 22 | 18 | 4 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0003 | 0/0 | 7434 | 8 | 8 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0004 | 0/0 | 7434 | 5 | 5 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0005 | 0/0 | 7434 | 4 | 4 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0007 | 0/0 | 7434 | 4 | 4 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0008 | 0/1 | 7429 | 3 | 0 | 2 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0009 | 0/0 | 7429 | 3 | 0 | 0 | 0 | 0 | 3 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0010 | 0/0 | 7429 | 3 | 0 | 0 | 0 | 0 | 3 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0012 | 0/0 | 7425 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0013 | 0/0 | 7429 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0014 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0015 | 0/0 | 7429 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0016 | 0/0 | 7429 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0017 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0018 | 0/0 | 7429 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0019 | 0/0 | 7429 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0020 | 0/0 | 7429 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0021 | 1/0 | 7429 | 1 | 0 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0022 | 0/0 | 7429 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0023 | 0/0 | 7429 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0024 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0025 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0026 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0027 | 0/0 | 7429 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0028 | 0/0 | 7429 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0001c0001t0029 | 0/0 | 7429 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0002c0002t0006 | 0/0 | 7434 | 4 | 4 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0002c0002t0011 | 0/0 | 7434 | 3 | 3 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
a0003c0003t0001 | 0/0 | 7429 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | copy fasta | chr16 | 47072703 | 47148945 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0003 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0008g0012 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0008g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0009g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0009g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0010g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0010g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0010g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0013g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0014g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0015g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0016g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0017g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0018g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0019g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0020g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0021g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0022g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0023g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0024g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0025g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0026g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0027g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0028g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0001c0001t0029g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0002c0002t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0002c0002t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0002c0002t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0002c0002t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0002c0002t0011g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0002c0002t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
a0003c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | GBR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | GBR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG00280 | hp2 | a0001 | c0001 | t0029 | g0142 | EUR | FIN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG00438 | hp1 | a0003 | c0003 | t0001 | g0040 | EAS | CHS | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG00741 | hp2 | a0001 | c0001 | t0008 | g0102 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01074 | hp1 | a0001 | c0001 | t0025 | g0137 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01081 | hp2 | a0001 | c0001 | t0020 | g0098 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01099 | hp1 | a0001 | c0001 | t0018 | g0049 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01358 | hp1 | a0001 | c0001 | t0008 | g0012 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01433 | hp2 | a0001 | c0001 | t0023 | g0078 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01496 | hp2 | a0001 | c0001 | t0024 | g0134 | AMR | CLM | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01884 | hp2 | a0002 | c0002 | t0011 | g0005 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG01891 | hp2 | a0001 | c0001 | t0026 | g0130 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02055 | hp1 | a0002 | c0002 | t0006 | g0021 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02132 | hp1 | a0001 | c0001 | t0019 | g0061 | EAS | KHV | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CDX | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0100 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0105 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02572 | hp1 | a0001 | c0001 | t0013 | g0017 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02572 | hp2 | a0001 | c0001 | t0012 | g0031 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02615 | hp1 | a0001 | c0001 | t0027 | g0140 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02683 | hp1 | a0001 | c0001 | t0028 | g0141 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02723 | hp1 | a0001 | c0001 | t0014 | g0143 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02735 | hp1 | a0001 | c0001 | t0015 | g0016 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02735 | hp2 | a0001 | c0001 | t0010 | g0057 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02886 | hp2 | a0001 | c0001 | t0022 | g0067 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02895 | hp2 | a0001 | c0001 | t0012 | g0034 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0076 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0106 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03041 | hp2 | a0002 | c0002 | t0011 | g0023 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03139 | hp2 | a0001 | c0001 | t0017 | g0097 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0107 | AFR | ESN | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03654 | hp2 | a0001 | c0001 | t0009 | g0007 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03704 | hp2 | a0001 | c0001 | t0009 | g0045 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03831 | hp2 | a0001 | c0001 | t0010 | g0109 | SAS | BEB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG04184 | hp1 | a0001 | c0001 | t0009 | g0007 | SAS | BEB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG04204 | hp1 | a0001 | c0001 | t0010 | g0051 | SAS | STU | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | STU | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0080 | AFR | YRI | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | YRI | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | LWK | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | LWK | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | LWK | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA19060 | hp2 | a0001 | c0001 | t0016 | g0056 | EAS | JPT | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | YRI | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA20129 | hp1 | a0002 | c0002 | t0011 | g0005 | AFR | ASW | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ASW | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02109 | hp1 | a0002 | c0002 | t0006 | g0020 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02486 | hp2 | a0001 | c0001 | t0013 | g0036 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG02559 | hp2 | a0002 | c0002 | t0006 | g0019 | AFR | ACB | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
HG03471 | hp2 | a0001 | c0001 | t0014 | g0144 | AFR | MSL | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA20300 | hp1 | a0002 | c0002 | t0006 | g0022 | AFR | USA | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | USA | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0008 | g0012 | REF | REF | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0021 | g0070 | REF | REF | NETO2_chr16_47072703_47148945 | NETO2 | chr16 | 47072703 | 47148945 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:47083433
|
A | T | 1 | a0002 | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
missense_variant | MODERATE | c.1366T>A | p.Ser456Thr | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 1699/7429 | 1366/1578 | 456/525 | chr16 | 47083433 | ||
chr16:47083489
|
T | A | 1 | a0003 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1310A>T | p.Asp437Val | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 1643/7429 | 1310/1578 | 437/525 | chr16 | 47083489 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:47077819
|
CTTCT | C | 1 | a0001c0001t0012 | 2 | HG02572.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5398_*5401delAGAA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 5398 | chr16 | 47077819 | |||||
chr16:47078669
|
A | C | 1 | a0001c0001t0009 | 3 | HG03654.hp2 HG03704.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4552T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 4552 | chr16 | 47078669 | |||||
chr16:47078784
|
C | A | 1 | a0001c0001t0003 | 8 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4437G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 4437 | chr16 | 47078784 | |||||
chr16:47079168
|
C | G | 1 | a0001c0001t0017 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4053G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 4053 | chr16 | 47079168 | |||||
chr16:47079318
|
A | G | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*3903T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 3903 | chr16 | 47079318 | |||||
chr16:47079636
|
G | A | 1 | a0002c0002t0006 | 4 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3585C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 3585 | chr16 | 47079636 | |||||
chr16:47079875
|
C | T | 1 | a0001c0001t0020 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3346G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 3346 | chr16 | 47079875 | |||||
chr16:47080040
|
G | C | 1 | a0001c0001t0026 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3181C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 3181 | chr16 | 47080040 | |||||
chr16:47080290
|
G | T | 1 | a0001c0001t0019 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2931C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2931 | chr16 | 47080290 | |||||
chr16:47080303
|
T | C | 1 | a0001c0001t0022 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2918A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2918 | chr16 | 47080303 | |||||
chr16:47080345
|
T | G | 1 | a0001c0001t0017 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2876A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2876 | chr16 | 47080345 | |||||
chr16:47080431
|
T | C | 2 | a0002c0002t0006a0002c0002t0011 | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2790A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2790 | chr16 | 47080431 | |||||
chr16:47080655
|
T | C | 1 | a0001c0001t0012 | 2 | HG02572.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2566A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2566 | chr16 | 47080655 | |||||
chr16:47080882
|
T | G | 1 | a0001c0001t0023 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2339A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2339 | chr16 | 47080882 | |||||
chr16:47080976
|
A | G | 1 | a0001c0001t0018 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2245T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2245 | chr16 | 47080976 | |||||
chr16:47080999
|
C | CTTCTG | 12 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(9): Show | 56 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2221_*2222insCAGA others(1): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2221 | chr16 | 47080999 | |||||
chr16:47081156
|
A | T | 1 | a0001c0001t0016 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2065T>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 2065 | chr16 | 47081156 | |||||
chr16:47081363
|
A | C | 1 | a0001c0001t0025 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1858T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 1858 | chr16 | 47081363 | |||||
chr16:47081865
|
T | C | 2 | a0002c0002t0006a0002c0002t0011 | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1356A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 1356 | chr16 | 47081865 | |||||
chr16:47082155
|
G | A | 1 | a0001c0001t0010 | 3 | HG02735.hp2 HG03831.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1066C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 1066 | chr16 | 47082155 | |||||
chr16:47082273
|
T | G | 10 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(7): Show | 51 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*948A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 948 | chr16 | 47082273 | |||||
chr16:47082304
|
T | C | 1 | a0001c0001t0007 | 4 | HG02280.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*917A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 917 | chr16 | 47082304 | |||||
chr16:47082553
|
C | T | 1 | a0001c0001t0024 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*668G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 668 | chr16 | 47082553 | |||||
chr16:47082768
|
T | C | 6 | a0001c0001t0002a0001c0001t0003a0001c0001t0014others(3): Show | 35 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*453A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 453 | chr16 | 47082768 | |||||
chr16:47082951
|
C | T | 1 | a0001c0001t0008 | 3 | HG00741.hp2 HG01358.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*270G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 270 | chr16 | 47082951 | |||||
chr16:47083021
|
G | C | 1 | a0001c0001t0013 | 2 | HG02486.hp2 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*200C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 9/9 | 200 | chr16 | 47083021 | |||||
chr16:47143668
|
G | C | 1 | a0001c0001t0027 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-56C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/9 | 56 | chr16 | 47143668 | |||||
chr16:47143677
|
G | A | 1 | a0001c0001t0028 | 1 | HG02683.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-65C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/9 | chr16 | 47143677 | ||||||
chr16:47143753
|
G | C | 1 | a0001c0001t0029 | 1 | HG00280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-141C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/9 | 141 | chr16 | 47143753 | |||||
chr16:47143780
|
G | A | 1 | a0001c0001t0014 | 2 | HG02723.hp1 HG03471.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-168C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/9 | chr16 | 47143780 | ||||||
chr16:47143908
|
A | G | 1 | a0001c0001t0015 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-296T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/9 | 296 | chr16 | 47143908 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:47083897
|
T | C | 32 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(29): Show | 35 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.998-96A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47083897 | ||||||
chr16:47084289
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.998-488C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47084289 | ||||||
chr16:47084405
|
CAGG | C | 1 | a0002c0002t0011g0005 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.998-607_998-605del others(3): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47084405 | ||||||
chr16:47084480
|
C | T | 1 | a0002c0002t0011g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.998-679G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47084480 | ||||||
chr16:47084526
|
C | G | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.998-725G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47084526 | ||||||
chr16:47084584
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.998-783A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47084584 | ||||||
chr16:47084990
|
T | C | 1 | a0001c0001t0014g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.998-1189A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47084990 | ||||||
chr16:47085016
|
A | G | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.997+1210T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085016 | ||||||
chr16:47085238
|
A | G | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.997+988T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085238 | ||||||
chr16:47085309
|
G | C | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.997+917C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085309 | ||||||
chr16:47085385
|
T | C | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.997+841A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085385 | ||||||
chr16:47085528
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.997+698G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085528 | ||||||
chr16:47085626
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.997+600G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085626 | ||||||
chr16:47085875
|
G | T | 2 | a0001c0001t0002g0135a0001c0001t0002g0136 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.997+351C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085875 | ||||||
chr16:47085979
|
AC | A | 2 | a0001c0001t0013g0017a0001c0001t0013g0036 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.997+246delG | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47085979 | ||||||
chr16:47086014
|
G | A | 1 | a0001c0001t0017g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.997+212C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47086014 | ||||||
chr16:47086037
|
C | T | 1 | a0001c0001t0001g0009 | 2 | HG02683.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.997+189G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 8/8 | chr16 | 47086037 | ||||||
chr16:47086779
|
T | C | 7 | a0001c0001t0003g0013a0001c0001t0003g0091a0001c0001t0003g0092others(4): Show | 8 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.884-440A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47086779 | ||||||
chr16:47086906
|
A | G | 1 | a0001c0001t0018g0049 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.884-567T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47086906 | ||||||
chr16:47086973
|
T | G | 2 | a0001c0001t0010g0051a0001c0001t0010g0057 | 2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.884-634A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47086973 | ||||||
chr16:47087032
|
AT | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.884-694delA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47087032 | ||||||
chr16:47087032
|
ATT | A | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.884-695_884-694del others(2): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47087032 | ||||||
chr16:47087078
|
G | C | 1 | a0001c0001t0007g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.884-739C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47087078 | ||||||
chr16:47087121
|
TG | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0058a0001c0001t0001g0060others(5): Show | 9 | HG00438.hp2 HG00642.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.884-783delC | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47087121 | ||||||
chr16:47087259
|
C | T | 37 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(34): Show | 41 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.884-920G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47087259 | ||||||
chr16:47087831
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.884-1492T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47087831 | ||||||
chr16:47088349
|
G | A | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.884-2010C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47088349 | ||||||
chr16:47088436
|
T | G | 1 | a0002c0002t0011g0005 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.884-2097A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47088436 | ||||||
chr16:47088453
|
G | A | 2 | a0001c0001t0004g0015a0001c0001t0004g0104 | 3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.884-2114C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47088453 | ||||||
chr16:47088808
|
G | T | 46 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(43): Show | 51 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.884-2469C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47088808 | ||||||
chr16:47089813
|
C | T | 43 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(40): Show | 48 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.884-3474G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47089813 | ||||||
chr16:47089943
|
T | A | 1 | a0001c0001t0029g0142 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.884-3604A>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47089943 | ||||||
chr16:47090352
|
TCACTGGT others(4): Show |
T | 1 | a0001c0001t0005g0081 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.884-4024_884-4014d others(13): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47090352 | ||||||
chr16:47090443
|
T | C | 43 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(40): Show | 48 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.884-4104A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47090443 | ||||||
chr16:47090729
|
C | A | 3 | a0001c0001t0010g0051a0001c0001t0010g0057a0001c0001t0010g0109 | 3 | HG02735.hp2 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.884-4390G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47090729 | ||||||
chr16:47090998
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.884-4659A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47090998 | ||||||
chr16:47091379
|
T | C | 2 | a0001c0001t0012g0031a0001c0001t0012g0034 | 2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.884-5040A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47091379 | ||||||
chr16:47091405
|
G | T | 1 | a0001c0001t0002g0120 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.884-5066C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47091405 | ||||||
chr16:47091463
|
T | C | 3 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127 | 3 | HG02257.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.884-5124A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47091463 | ||||||
chr16:47091828
|
G | A | 44 | a0001c0001t0001g0058a0001c0001t0002g0004a0001c0001t0002g0116others(41): Show | 49 | HG00642.hp1 HG00735.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.884-5489C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47091828 | ||||||
chr16:47092025
|
G | GT | 11 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0052others(8): Show | 11 | HG00642.hp1 HG01169.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.884-5687dupA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47092025 | ||||||
chr16:47092025
|
G | T | 1 | a0001c0001t0005g0076 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.884-5686C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47092025 | ||||||
chr16:47092502
|
C | T | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.884-6163G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47092502 | ||||||
chr16:47092542
|
G | C | 34 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(31): Show | 38 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.884-6203C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47092542 | ||||||
chr16:47093068
|
C | T | 2 | a0001c0001t0004g0015a0001c0001t0004g0104 | 3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.884-6729G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47093068 | ||||||
chr16:47093466
|
A | G | 2 | a0001c0001t0004g0015a0001c0001t0004g0104 | 3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.884-7127T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47093466 | ||||||
chr16:47093622
|
T | C | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.884-7283A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47093622 | ||||||
chr16:47093667
|
T | C | 1 | a0001c0001t0023g0078 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.884-7328A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47093667 | ||||||
chr16:47093842
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.884-7503G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47093842 | ||||||
chr16:47093896
|
A | G | 2 | a0001c0001t0004g0015a0001c0001t0004g0104 | 3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.884-7557T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47093896 | ||||||
chr16:47094041
|
A | G | 1 | a0003c0003t0001g0040 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.884-7702T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094041 | ||||||
chr16:47094193
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.884-7854G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094193 | ||||||
chr16:47094247
|
C | T | 2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.884-7908G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094247 | ||||||
chr16:47094263
|
A | AT | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.884-7925dupA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094263 | ||||||
chr16:47094263
|
A | ATT | 5 | a0001c0001t0002g0133a0001c0001t0007g0105a0001c0001t0007g0106others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.884-7926_884-7925d others(4): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094263 | ||||||
chr16:47094263
|
A | ATTT | 7 | a0001c0001t0002g0120a0001c0001t0004g0024a0001c0001t0004g0025others(4): Show | 7 | HG01361.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.884-7927_884-7925d others(5): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094263 | ||||||
chr16:47094403
|
T | TTTTA | 37 | a0001c0001t0002g0004a0001c0001t0002g0117a0001c0001t0002g0118others(34): Show | 41 | HG00735.hp2 HG01109.hp2 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.884-8068_884-8065d others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094403 | ||||||
chr16:47094403
|
T | TTTTATTT others(1): Show |
4 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(1): Show | 4 | HG01074.hp1 HG01361.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.884-8072_884-8065d others(10): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094403 | ||||||
chr16:47094408
|
TTTATTTA others(1): Show |
T | 3 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021 | 3 | HG02055.hp1 HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.884-8077_884-8070d others(10): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094408 | ||||||
chr16:47094416
|
C | CTTAT | 2 | a0001c0001t0001g0030a0001c0001t0001g0058 | 2 | HG00642.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.884-8081_884-8078d others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094416 | ||||||
chr16:47094416
|
C | T | 43 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(40): Show | 48 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.884-8077G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094416 | ||||||
chr16:47094437
|
T | C | 2 | a0001c0001t0012g0031a0001c0001t0012g0034 | 2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.884-8098A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094437 | ||||||
chr16:47094526
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0111 | 2 | HG00140.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.884-8187G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094526 | ||||||
chr16:47094672
|
C | T | 1 | a0001c0001t0009g0007 | 2 | HG03654.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.884-8333G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47094672 | ||||||
chr16:47095266
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.884-8927T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47095266 | ||||||
chr16:47095278
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.884-8939T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47095278 | ||||||
chr16:47095645
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.884-9306C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47095645 | ||||||
chr16:47096150
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.884-9811T>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47096150 | ||||||
chr16:47096154
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.884-9815G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47096154 | ||||||
chr16:47096271
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.884-9932G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47096271 | ||||||
chr16:47096322
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.884-9983A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47096322 | ||||||
chr16:47096881
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.884-10542C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47096881 | ||||||
chr16:47096912
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 19 | HG00735.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.884-10573G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47096912 | ||||||
chr16:47097140
|
C | A | 2 | a0001c0001t0008g0012a0001c0001t0008g0102 | 3 | HG00741.hp2 HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.884-10801G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097140 | ||||||
chr16:47097141
|
C | T | 2 | a0001c0001t0004g0015a0001c0001t0004g0104 | 3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.884-10802G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097141 | ||||||
chr16:47097365
|
G | C | 1 | a0001c0001t0004g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.884-11026C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097365 | ||||||
chr16:47097535
|
A | G | 1 | a0001c0001t0017g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.884-11196T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097535 | ||||||
chr16:47097549
|
T | C | 1 | a0001c0001t0004g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.884-11210A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097549 | ||||||
chr16:47097864
|
A | G | 5 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-11525T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097864 | ||||||
chr16:47097928
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.883+11555T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47097928 | ||||||
chr16:47098318
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.883+11165A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47098318 | ||||||
chr16:47098371
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0027g0140 | 3 | HG01884.hp1 HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883+11112G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47098371 | ||||||
chr16:47098888
|
T | G | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.883+10595A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47098888 | ||||||
chr16:47098951
|
G | T | 1 | a0001c0001t0001g0087 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.883+10532C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47098951 | ||||||
chr16:47098984
|
C | T | 1 | a0001c0001t0002g0128 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.883+10499G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47098984 | ||||||
chr16:47099328
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.883+10155C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47099328 | ||||||
chr16:47099450
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.883+10033G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47099450 | ||||||
chr16:47099581
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.883+9902T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47099581 | ||||||
chr16:47101022
|
C | A | 1 | a0001c0001t0004g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.883+8461G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47101022 | ||||||
chr16:47101039
|
G | C | 31 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(28): Show | 35 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.883+8444C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47101039 | ||||||
chr16:47101622
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.883+7861T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47101622 | ||||||
chr16:47102034
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.883+7449A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102034 | ||||||
chr16:47102253
|
C | T | 1 | a0001c0001t0005g0076 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.883+7230G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102253 | ||||||
chr16:47102607
|
A | AC | 26 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(23): Show | 29 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.883+6875dupG | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102607 | ||||||
chr16:47102607
|
A | C | 16 | a0001c0001t0002g0118a0001c0001t0002g0119a0001c0001t0004g0015others(13): Show | 18 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.883+6876T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102607 | ||||||
chr16:47102611
|
C | A | 1 | a0002c0002t0011g0005 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.883+6872G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102611 | ||||||
chr16:47102756
|
C | T | 29 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(26): Show | 32 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.883+6727G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102756 | ||||||
chr16:47102838
|
T | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.883+6645A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102838 | ||||||
chr16:47102844
|
G | A | 1 | a0001c0001t0004g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.883+6639C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102844 | ||||||
chr16:47102883
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.883+6600C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47102883 | ||||||
chr16:47103082
|
C | T | 1 | a0001c0001t0012g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.883+6401G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47103082 | ||||||
chr16:47103929
|
C | T | 1 | a0001c0001t0017g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.883+5554G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47103929 | ||||||
chr16:47104737
|
T | C | 2 | a0001c0001t0004g0015a0001c0001t0004g0104 | 3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.883+4746A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47104737 | ||||||
chr16:47105025
|
T | TTTTC | 46 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(43): Show | 51 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.883+4457_883+4458i others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47105025 | ||||||
chr16:47106069
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0114 | 2 | HG03654.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.883+3414A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47106069 | ||||||
chr16:47106109
|
ACATGGAT others(17): Show |
A | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.883+3350_883+3373d others(26): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47106109 | ||||||
chr16:47106287
|
A | G | 1 | a0001c0001t0002g0123 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.883+3196T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47106287 | ||||||
chr16:47106729
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.883+2754A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47106729 | ||||||
chr16:47106927
|
G | A | 7 | a0001c0001t0003g0013a0001c0001t0003g0091a0001c0001t0003g0092others(4): Show | 8 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.883+2556C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47106927 | ||||||
chr16:47107303
|
C | G | 43 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(40): Show | 48 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.883+2180G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47107303 | ||||||
chr16:47107589
|
C | T | 1 | a0001c0001t0004g0015 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.883+1894G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47107589 | ||||||
chr16:47107621
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.883+1862A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47107621 | ||||||
chr16:47108313
|
T | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.883+1170A>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47108313 | ||||||
chr16:47108375
|
T | A | 1 | a0001c0001t0004g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.883+1108A>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47108375 | ||||||
chr16:47108560
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0005g0076 | 2 | HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.883+923A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47108560 | ||||||
chr16:47108597
|
G | T | 3 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0005g0082 | 3 | HG01891.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.883+886C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47108597 | ||||||
chr16:47108792
|
G | C | 3 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127 | 3 | HG02257.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.883+691C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47108792 | ||||||
chr16:47109381
|
AAC | A | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.883+100_883+101del others(2): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47109381 | ||||||
chr16:47109470
|
ATTAT | A | 2 | a0001c0001t0001g0018a0001c0001t0013g0017 | 2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.883+9_883+12delATA others(1): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 7/8 | chr16 | 47109470 | ||||||
chr16:47109762
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.655-51T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47109762 | ||||||
chr16:47110006
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0058a0001c0001t0001g0060others(5): Show | 9 | HG00438.hp2 HG00642.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.655-295A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47110006 | ||||||
chr16:47110385
|
A | G | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-674T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47110385 | ||||||
chr16:47110391
|
C | G | 1 | a0001c0001t0028g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.655-680G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47110391 | ||||||
chr16:47110637
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0023g0078 | 3 | HG00642.hp2 HG00741.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.655-926A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47110637 | ||||||
chr16:47111538
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.655-1827A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47111538 | ||||||
chr16:47111586
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.655-1875G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47111586 | ||||||
chr16:47111597
|
C | A | 1 | a0002c0002t0011g0005 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.655-1886G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47111597 | ||||||
chr16:47111708
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.655-1997C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47111708 | ||||||
chr16:47111771
|
G | A | 1 | a0001c0001t0004g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.655-2060C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47111771 | ||||||
chr16:47111822
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.655-2111C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47111822 | ||||||
chr16:47112381
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.655-2670G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112381 | ||||||
chr16:47112428
|
G | A | 1 | a0001c0001t0029g0142 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.655-2717C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112428 | ||||||
chr16:47112526
|
T | C | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-2815A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112526 | ||||||
chr16:47112807
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 19 | HG00735.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.655-3096T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112807 | ||||||
chr16:47112836
|
G | A | 2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.655-3125C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112836 | ||||||
chr16:47112869
|
ATT | A | 2 | a0001c0001t0001g0014a0001c0001t0027g0140 | 3 | HG01884.hp1 HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.655-3160_655-3159d others(4): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112869 | ||||||
chr16:47112869
|
ATTGT | A | 2 | a0001c0001t0012g0031a0001c0001t0012g0034 | 2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.655-3162_655-3159d others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112869 | ||||||
chr16:47112976
|
T | C | 1 | a0001c0001t0020g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.655-3265A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47112976 | ||||||
chr16:47113212
|
T | C | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-3501A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113212 | ||||||
chr16:47113216
|
A | C | 1 | a0001c0001t0007g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.655-3505T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113216 | ||||||
chr16:47113386
|
C | T | 2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.655-3675G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113386 | ||||||
chr16:47113560
|
C | T | 1 | a0001c0001t0022g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.655-3849G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113560 | ||||||
chr16:47113585
|
C | CT | 14 | a0001c0001t0001g0053a0001c0001t0001g0064a0001c0001t0001g0079others(11): Show | 15 | HG01255.hp1 HG01884.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.655-3875dupA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113585 | ||||||
chr16:47113585
|
CT | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0115a0001c0001t0002g0131others(1): Show | 5 | HG00280.hp1 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-3875delA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113585 | ||||||
chr16:47113753
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.655-4042C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47113753 | ||||||
chr16:47114085
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.655-4374G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114085 | ||||||
chr16:47114207
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0138 | 3 | HG03098.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.655-4496A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114207 | ||||||
chr16:47114365
|
C | CT | 20 | a0001c0001t0001g0014a0001c0001t0001g0052a0001c0001t0002g0131others(17): Show | 22 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.655-4655dupA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114365 | ||||||
chr16:47114365
|
C | CTT | 25 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(22): Show | 28 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.655-4656_655-4655d others(4): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114365 | ||||||
chr16:47114379
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.655-4668A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114379 | ||||||
chr16:47114439
|
C | CT | 12 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(9): Show | 12 | HG00438.hp1 HG00642.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.655-4729dupA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114439 | ||||||
chr16:47114439
|
CT | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0073others(33): Show | 43 | HG00280.hp1 HG01074.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.655-4729delA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114439 | ||||||
chr16:47114439
|
CTT | C | 10 | a0001c0001t0002g0133a0001c0001t0003g0091a0001c0001t0004g0015others(7): Show | 11 | HG02109.hp2 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.655-4730_655-4729d others(4): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114439 | ||||||
chr16:47114448
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.655-4737A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114448 | ||||||
chr16:47114532
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.655-4821C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114532 | ||||||
chr16:47114600
|
G | A | 6 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0112others(3): Show | 6 | HG00438.hp2 HG00642.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-4889C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114600 | ||||||
chr16:47114851
|
A | G | 2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.655-5140T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114851 | ||||||
chr16:47114946
|
C | A | 2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.655-5235G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47114946 | ||||||
chr16:47115236
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 141 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.655-5525T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115236 | ||||||
chr16:47115590
|
C | T | 43 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(40): Show | 48 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.655-5879G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115590 | ||||||
chr16:47115697
|
T | TTATATAT others(25): Show |
1 | a0001c0001t0002g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.655-5987_655-5986i others(34): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115697 | ||||||
chr16:47115700
|
T | TATATATA others(7): Show |
4 | a0001c0001t0007g0105a0001c0001t0007g0106a0001c0001t0007g0107others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-6003_655-5990d others(16): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115700 | ||||||
chr16:47115701
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0010g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.655-6024_655-5991d others(36): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115701 | ||||||
chr16:47115714
|
C | CATATATA others(25): Show |
2 | a0002c0002t0006g0019a0002c0002t0006g0020 | 2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.655-6004_655-6003i others(34): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115714 | ||||||
chr16:47115714
|
C | CATATATA others(27): Show |
1 | a0002c0002t0006g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.655-6004_655-6003i others(36): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115714 | ||||||
chr16:47115714
|
C | CATATATA others(49): Show |
1 | a0002c0002t0006g0022 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.655-6004_655-6003i others(58): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115714 | ||||||
chr16:47115714
|
C | CATATATA others(43): Show |
1 | a0002c0002t0011g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.655-6004_655-6003i others(52): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115714 | ||||||
chr16:47115714
|
CATAT | C | 5 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0005g0081others(2): Show | 5 | HG01496.hp2 HG01891.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-6007_655-6004d others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115714 | ||||||
chr16:47115716
|
T | TATATATA others(5): Show |
2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.655-6006_655-6005i others(14): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | ||||||
chr16:47115716
|
T | TATATATA others(157): Show |
1 | a0001c0001t0004g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655-6006_655-6005i others(166): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | ||||||
chr16:47115716
|
T | TATATATA others(23): Show |
2 | a0001c0001t0002g0120a0001c0001t0003g0100 | 2 | HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.655-6006_655-6005i others(32): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | ||||||
chr16:47115716
|
T | TATATATA others(53): Show |
1 | a0001c0001t0002g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.655-6006_655-6005i others(62): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | ||||||
chr16:47115716
|
T | TATATATA others(23): Show |
17 | a0001c0001t0002g0004a0001c0001t0002g0117a0001c0001t0002g0118others(14): Show | 20 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.655-6006_655-6005i others(32): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | ||||||
chr16:47115716
|
T | TATATATA others(55): Show |
4 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0129others(1): Show | 4 | HG01891.hp2 HG02258.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-6006_655-6005i others(64): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | ||||||
chr16:47115716
|
T | TATATATA others(25): Show |
1 | a0001c0001t0002g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.655-6006_655-6005i others(34): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | ||||||
chr16:47115716
|
T | TATATATA others(170): Show |
1 | a0001c0001t0004g0015 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.655-6006_655-6005i others(179): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115716 | ||||||
chr16:47115717
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.655-6006T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115717 | ||||||
chr16:47115718
|
T | C | 1 | a0001c0001t0005g0080 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.655-6007A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115718 | ||||||
chr16:47115718
|
T | TATATATA others(21): Show |
3 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0095 | 3 | HG02922.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.655-6008_655-6007i others(30): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115718 | ||||||
chr16:47115718
|
T | TATATATA others(17): Show |
1 | a0001c0001t0017g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.655-6008_655-6007i others(26): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115718 | ||||||
chr16:47115732
|
C | T | 43 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(40): Show | 48 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.655-6021G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115732 | ||||||
chr16:47115734
|
T | TATATATG others(75): Show |
1 | a0002c0002t0011g0005 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.655-6024_655-6023i others(84): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115734 | ||||||
chr16:47115785
|
G | T | 1 | a0001c0001t0001g0050 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.655-6074C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115785 | ||||||
chr16:47115919
|
CTGATA | C | 2 | a0001c0001t0001g0099a0001c0001t0029g0142 | 2 | HG00280.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.655-6213_655-6209d others(7): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47115919 | ||||||
chr16:47116014
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0023g0078 | 3 | HG00642.hp2 HG00741.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.655-6303A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116014 | ||||||
chr16:47116031
|
T | C | 1 | a0001c0001t0001g0006 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.655-6320A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116031 | ||||||
chr16:47116140
|
C | G | 1 | a0001c0001t0007g0108 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.655-6429G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116140 | ||||||
chr16:47116142
|
G | GTT | 6 | a0001c0001t0007g0105a0002c0002t0006g0019a0002c0002t0006g0020others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-6433_655-6432d others(4): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116142 | ||||||
chr16:47116142
|
GT | G | 26 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(23): Show | 29 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.655-6432delA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116142 | ||||||
chr16:47116346
|
G | C | 7 | a0001c0001t0003g0013a0001c0001t0003g0091a0001c0001t0003g0092others(4): Show | 8 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+6311C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116346 | ||||||
chr16:47116945
|
G | T | 36 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(33): Show | 40 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.654+5712C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116945 | ||||||
chr16:47116964
|
C | G | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+5693G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47116964 | ||||||
chr16:47117028
|
T | C | 1 | a0001c0001t0002g0004 | 3 | HG02895.hp1 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.654+5629A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47117028 | ||||||
chr16:47117146
|
C | G | 2 | a0001c0001t0014g0143a0001c0001t0014g0144 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.654+5511G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47117146 | ||||||
chr16:47117341
|
T | C | 1 | a0001c0001t0003g0094 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.654+5316A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47117341 | ||||||
chr16:47117422
|
T | C | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+5235A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47117422 | ||||||
chr16:47117763
|
G | A | 1 | a0001c0001t0001g0009 | 2 | HG02683.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.654+4894C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47117763 | ||||||
chr16:47117917
|
T | C | 40 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(37): Show | 44 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.654+4740A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47117917 | ||||||
chr16:47118003
|
C | T | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.654+4654G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47118003 | ||||||
chr16:47118195
|
CTTTG | C | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+4458_654+4461d others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47118195 | ||||||
chr16:47118510
|
A | C | 2 | a0001c0001t0007g0106a0001c0001t0007g0107 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.654+4147T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47118510 | ||||||
chr16:47118723
|
CTTATT | C | 2 | a0001c0001t0004g0015a0001c0001t0004g0104 | 3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.654+3929_654+3933d others(7): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47118723 | ||||||
chr16:47119276
|
T | C | 1 | a0001c0001t0015g0016 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.654+3381A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47119276 | ||||||
chr16:47119297
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.654+3360C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47119297 | ||||||
chr16:47119376
|
T | C | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.654+3281A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47119376 | ||||||
chr16:47119714
|
G | T | 1 | a0001c0001t0019g0061 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.654+2943C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47119714 | ||||||
chr16:47119741
|
A | G | 32 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(29): Show | 35 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.654+2916T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47119741 | ||||||
chr16:47121021
|
T | A | 7 | a0001c0001t0003g0013a0001c0001t0003g0091a0001c0001t0003g0092others(4): Show | 8 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+1636A>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47121021 | ||||||
chr16:47121380
|
G | T | 1 | a0001c0001t0017g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.654+1277C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47121380 | ||||||
chr16:47121456
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.654+1201C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47121456 | ||||||
chr16:47121730
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.654+927G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47121730 | ||||||
chr16:47122098
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.654+559A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47122098 | ||||||
chr16:47122239
|
G | C | 1 | a0002c0002t0011g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.654+418C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47122239 | ||||||
chr16:47122359
|
T | C | 38 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(35): Show | 42 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.654+298A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47122359 | ||||||
chr16:47122637
|
G | A | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.654+20C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 6/8 | chr16 | 47122637 | ||||||
chr16:47123001
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.482-89A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123001 | ||||||
chr16:47123011
|
A | G | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.482-99T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123011 | ||||||
chr16:47123024
|
T | C | 2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.482-112A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123024 | ||||||
chr16:47123062
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.482-150C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123062 | ||||||
chr16:47123459
|
C | T | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-547G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123459 | ||||||
chr16:47123573
|
T | G | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-661A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123573 | ||||||
chr16:47123993
|
G | A | 1 | a0001c0001t0003g0095 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.482-1081C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47123993 | ||||||
chr16:47124682
|
A | T | 7 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0005g0080others(4): Show | 7 | HG01496.hp2 HG01891.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-1770T>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47124682 | ||||||
chr16:47124955
|
G | A | 30 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(27): Show | 33 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.482-2043C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47124955 | ||||||
chr16:47125007
|
AAAGT | A | 22 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(19): Show | 24 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.482-2099_482-2096d others(6): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125007 | ||||||
chr16:47125064
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.482-2152T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125064 | ||||||
chr16:47125211
|
G | C | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-2299C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125211 | ||||||
chr16:47125349
|
G | GT | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-2438dupA | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125349 | ||||||
chr16:47125364
|
C | A | 3 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127 | 3 | HG02257.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.482-2452G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125364 | ||||||
chr16:47125535
|
G | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0023g0078 | 3 | HG00642.hp2 HG00741.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.482-2623C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125535 | ||||||
chr16:47125556
|
G | T | 3 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127 | 3 | HG02257.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.482-2644C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125556 | ||||||
chr16:47125760
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.481+2565T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47125760 | ||||||
chr16:47126821
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.481+1504C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47126821 | ||||||
chr16:47126892
|
A | C | 1 | a0001c0001t0001g0010 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.481+1433T>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47126892 | ||||||
chr16:47126900
|
C | A | 36 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(33): Show | 40 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.481+1425G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47126900 | ||||||
chr16:47127149
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.481+1176G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47127149 | ||||||
chr16:47127338
|
C | T | 1 | a0001c0001t0013g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.481+987G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47127338 | ||||||
chr16:47127434
|
TAC | T | 2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.481+889_481+890del others(2): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47127434 | ||||||
chr16:47127436
|
C | G | 1 | a0001c0001t0005g0080 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.481+889G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47127436 | ||||||
chr16:47127555
|
G | T | 29 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(26): Show | 32 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.481+770C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47127555 | ||||||
chr16:47127588
|
T | C | 2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.481+737A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 4/8 | chr16 | 47127588 | ||||||
chr16:47128745
|
C | T | 1 | a0001c0001t0004g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.233-172G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 3/8 | chr16 | 47128745 | ||||||
chr16:47129380
|
C | A | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-16G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47129380 | ||||||
chr16:47129404
|
A | G | 14 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(11): Show | 16 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.92-40T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47129404 | ||||||
chr16:47129814
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.92-450G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47129814 | ||||||
chr16:47129963
|
C | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(39): Show | 52 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.92-599G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47129963 | ||||||
chr16:47130417
|
G | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0035others(3): Show | 9 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.92-1053C>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47130417 | ||||||
chr16:47130456
|
A | ATAAC | 6 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0035others(3): Show | 9 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.92-1093_92-1092ins others(4): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47130456 | ||||||
chr16:47130469
|
T | A | 1 | a0001c0001t0007g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92-1105A>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47130469 | ||||||
chr16:47130668
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.91+1301C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47130668 | ||||||
chr16:47130938
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.91+1031C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47130938 | ||||||
chr16:47131074
|
G | GA | 5 | a0001c0001t0001g0099a0001c0001t0004g0015a0001c0001t0004g0104others(2): Show | 6 | HG00280.hp2 HG01496.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+894dupT | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47131074 | ||||||
chr16:47131092
|
T | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0103 | 3 | HG02071.hp2 NA18948.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.91+877A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47131092 | ||||||
chr16:47131455
|
T | C | 1 | a0001c0001t0019g0061 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.91+514A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47131455 | ||||||
chr16:47131935
|
A | G | 2 | a0001c0001t0004g0015a0001c0001t0004g0104 | 3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.91+34T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 2/8 | chr16 | 47131935 | ||||||
chr16:47132447
|
G | A | 3 | a0001c0001t0007g0106a0001c0001t0007g0107a0001c0001t0007g0108 | 3 | HG02818.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.35-422C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47132447 | ||||||
chr16:47132506
|
C | A | 1 | a0001c0001t0002g0119 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.35-481G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47132506 | ||||||
chr16:47132792
|
C | T | 4 | a0001c0001t0007g0105a0001c0001t0007g0106a0001c0001t0007g0107others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-767G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47132792 | ||||||
chr16:47133558
|
C | G | 3 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0005g0082 | 3 | HG01891.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.35-1533G>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133558 | ||||||
chr16:47133604
|
C | A | 1 | a0001c0001t0029g0142 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.35-1579G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | ||||||
chr16:47133604
|
C | CATAAA | 7 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0101others(4): Show | 10 | HG00741.hp2 HG01071.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.35-1584_35-1580dup others(5): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | ||||||
chr16:47133604
|
C | CATAAAAT others(3): Show |
1 | a0001c0001t0001g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.35-1589_35-1580dup others(10): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | ||||||
chr16:47133604
|
C | CATAAAAT others(18): Show |
3 | a0001c0001t0007g0106a0001c0001t0007g0107a0001c0001t0007g0108 | 3 | HG02818.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.35-1604_35-1580dup others(25): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | ||||||
chr16:47133604
|
CATAAA | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(68): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.35-1584_35-1580del others(5): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | ||||||
chr16:47133604
|
CATAAAAT others(3): Show |
C | 20 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0075others(17): Show | 22 | HG00735.hp2 HG01074.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.35-1589_35-1580del others(10): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | ||||||
chr16:47133604
|
CATAAAAT others(8): Show |
C | 5 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0079others(2): Show | 5 | HG01074.hp2 HG01169.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-1594_35-1580del others(15): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | ||||||
chr16:47133604
|
CATAAAAT others(13): Show |
C | 5 | a0001c0001t0002g0118a0002c0002t0006g0019a0002c0002t0006g0020others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-1599_35-1580del others(20): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | ||||||
chr16:47133604
|
CATAAAAT others(18): Show |
C | 2 | a0001c0001t0004g0015a0001c0001t0004g0104 | 3 | HG02970.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.35-1604_35-1580del others(25): Show |
NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133604 | ||||||
chr16:47133750
|
A | G | 39 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(36): Show | 43 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.35-1725T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133750 | ||||||
chr16:47133897
|
C | T | 1 | a0001c0001t0012g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.35-1872G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133897 | ||||||
chr16:47133994
|
C | CA | 6 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(3): Show | 6 | HG01496.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.35-1970dupT | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47133994 | ||||||
chr16:47134233
|
T | TA | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0005g0076 | 3 | HG02615.hp2 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.35-2209dupT | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47134233 | ||||||
chr16:47134355
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.35-2330C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47134355 | ||||||
chr16:47134701
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.35-2676G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47134701 | ||||||
chr16:47134882
|
T | C | 22 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(19): Show | 24 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.35-2857A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47134882 | ||||||
chr16:47135069
|
G | C | 1 | a0001c0001t0001g0074 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.35-3044C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47135069 | ||||||
chr16:47135071
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0005g0076 | 2 | HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.35-3046A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47135071 | ||||||
chr16:47135690
|
G | C | 1 | a0001c0001t0004g0015 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.35-3665C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47135690 | ||||||
chr16:47136390
|
T | C | 1 | a0001c0001t0002g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.35-4365A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47136390 | ||||||
chr16:47136825
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.35-4800A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47136825 | ||||||
chr16:47136910
|
C | T | 1 | a0001c0001t0023g0078 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.35-4885G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47136910 | ||||||
chr16:47137070
|
C | T | 1 | a0002c0002t0011g0005 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.35-5045G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47137070 | ||||||
chr16:47137422
|
T | C | 71 | a0001c0001t0001g0014a0001c0001t0001g0079a0001c0001t0001g0083others(68): Show | 77 | HG00140.hp2 HG00280.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.35-5397A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47137422 | ||||||
chr16:47137442
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.35-5417G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47137442 | ||||||
chr16:47138019
|
G | A | 25 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(22): Show | 27 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.34+5560C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138019 | ||||||
chr16:47138039
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.34+5540C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138039 | ||||||
chr16:47138128
|
G | A | 1 | a0001c0001t0008g0102 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.34+5451C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138128 | ||||||
chr16:47138192
|
A | G | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+5387T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138192 | ||||||
chr16:47138257
|
G | A | 3 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0024g0134 | 3 | HG01496.hp2 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.34+5322C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138257 | ||||||
chr16:47138272
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(1): Show | 4 | HG00408.hp1 HG02071.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+5307G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138272 | ||||||
chr16:47138324
|
T | C | 3 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0024g0134 | 3 | HG01496.hp2 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.34+5255A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138324 | ||||||
chr16:47138591
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.34+4988G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138591 | ||||||
chr16:47138750
|
T | C | 33 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(30): Show | 36 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.34+4829A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138750 | ||||||
chr16:47138809
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.34+4770A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47138809 | ||||||
chr16:47139067
|
T | G | 39 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(36): Show | 43 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.34+4512A>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47139067 | ||||||
chr16:47139103
|
G | A | 1 | a0001c0001t0010g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.34+4476C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47139103 | ||||||
chr16:47139885
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.34+3694A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47139885 | ||||||
chr16:47140133
|
G | C | 6 | a0002c0002t0006g0019a0002c0002t0006g0020a0002c0002t0006g0021others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+3446C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47140133 | ||||||
chr16:47140152
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.34+3427G>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47140152 | ||||||
chr16:47140364
|
A | G | 25 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(22): Show | 27 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.34+3215T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47140364 | ||||||
chr16:47140728
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.34+2851A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47140728 | ||||||
chr16:47141041
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.34+2538T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47141041 | ||||||
chr16:47141244
|
G | C | 1 | a0001c0001t0004g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.34+2335C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47141244 | ||||||
chr16:47141273
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.34+2306A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47141273 | ||||||
chr16:47141373
|
T | A | 1 | a0001c0001t0001g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.34+2206A>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47141373 | ||||||
chr16:47141381
|
G | C | 1 | a0001c0001t0025g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.34+2198C>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47141381 | ||||||
chr16:47141781
|
A | G | 2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.34+1798T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47141781 | ||||||
chr16:47142140
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.34+1439A>G | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47142140 | ||||||
chr16:47142413
|
A | G | 8 | a0001c0001t0014g0143a0001c0001t0014g0144a0002c0002t0006g0019others(5): Show | 9 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.34+1166T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47142413 | ||||||
chr16:47142447
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0013g0017 | 2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.34+1132G>A | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47142447 | ||||||
chr16:47142547
|
A | G | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.34+1032T>C | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47142547 | ||||||
chr16:47143431
|
G | A | 25 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0117others(22): Show | 27 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.34+148C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47143431 | ||||||
chr16:47143491
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.34+88C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47143491 | ||||||
chr16:47143524
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.34+55C>T | NETO2 | ENSG00000171208.10 | transcript | ENST00000562435.6 | protein_coding | 1/8 | chr16 | 47143524 |