geneid | 9683 |
---|---|
ensemblid | ENSG00000102921.8 |
hgncid | 29850 |
symbol | N4BP1 |
name | NEDD4 binding protein 1 |
refseq_nuc | NM_153029.4 |
refseq_prot | NP_694574.3 |
ensembl_nuc | ENST00000262384.4 |
ensembl_prot | ENSP00000262384.3 |
mane_status | MANE Select |
chr | chr16 |
start | 48538726 |
end | 48610180 |
strand | - |
ver | v1.2 |
region | chr16:48538726-48610180 |
region5000 | chr16:48533726-48615180 |
regionname0 | N4BP1_chr16_48538726_48610180 |
regionname5000 | N4BP1_chr16_48533726_48615180 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 896 | 317 | 80 | 57 | 133 | 14 | 31 | 109 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0002 | 0/0 | 896 | 4 | 0 | 1 | 3 | 0 | 0 | 3 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0003 | 0/0 | 896 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0004 | 0/0 | 896 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2691 | 303 | 67 | 57 | 132 | 14 | 31 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
c0002 | 0/0 | 2691 | 9 | 9 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
c0003 | 0/0 | 2691 | 4 | 0 | 1 | 3 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
c0004 | 0/0 | 2691 | 3 | 3 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
c0005 | 0/0 | 2691 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
c0006 | 0/0 | 2691 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
c0007 | 0/0 | 2691 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
c0008 | 0/0 | 2691 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4386 | 114 | 23 | 22 | 46 | 5 | 18 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0002 | 0/0 | 4387 | 86 | 2 | 12 | 66 | 2 | 4 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0003 | 1/1 | 4387 | 70 | 17 | 16 | 20 | 7 | 8 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0004 | 0/0 | 4386 | 9 | 9 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0005 | 0/0 | 4387 | 8 | 8 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0006 | 0/0 | 4386 | 5 | 4 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0007 | 0/0 | 4386 | 5 | 5 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0008 | 0/0 | 4387 | 4 | 0 | 4 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0009 | 0/0 | 4387 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0010 | 0/0 | 4387 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0011 | 0/0 | 4387 | 2 | 0 | 2 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0012 | 0/0 | 4386 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0013 | 0/0 | 4387 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0014 | 0/0 | 4387 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0015 | 0/0 | 4387 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0016 | 0/0 | 4387 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0017 | 0/0 | 4387 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0018 | 0/0 | 4387 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0019 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0020 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0021 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0022 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0023 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0024 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0025 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0026 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
t0027 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0006 | 0/1 | 3 | 0 | 1 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0014 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2691 | 303 | 67 | 57 | 132 | 14 | 31 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0002 | 0/0 | 2691 | 9 | 9 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0004 | 0/0 | 2691 | 3 | 3 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0007 | 0/0 | 2691 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0008 | 0/0 | 2691 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0002c0003 | 0/0 | 2691 | 4 | 0 | 1 | 3 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0003c0005 | 0/0 | 2691 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0004c0006 | 0/0 | 2691 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7076 | 111 | 22 | 22 | 45 | 5 | 17 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0002 | 0/0 | 7077 | 82 | 2 | 11 | 63 | 2 | 4 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0003 | 1/1 | 7077 | 65 | 12 | 16 | 20 | 7 | 8 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0005 | 0/0 | 7077 | 8 | 8 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0006 | 0/0 | 7076 | 5 | 4 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0007 | 0/0 | 7076 | 5 | 5 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0008 | 0/0 | 7077 | 4 | 0 | 4 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0009 | 0/0 | 7077 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0010 | 0/0 | 7077 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0011 | 0/0 | 7077 | 2 | 0 | 2 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0012 | 0/0 | 7076 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0013 | 0/0 | 7077 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0014 | 0/0 | 7077 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0015 | 0/0 | 7077 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0016 | 0/0 | 7077 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0017 | 0/0 | 7077 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0018 | 0/0 | 7077 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0019 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0020 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0021 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0022 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0023 | 0/0 | 7076 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0024 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0025 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0026 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0001t0027 | 0/0 | 7058 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0002t0004 | 0/0 | 7076 | 9 | 9 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0004t0003 | 0/0 | 7077 | 3 | 3 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0007t0001 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0001c0008t0001 | 0/0 | 7076 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0002c0003t0002 | 0/0 | 7077 | 4 | 0 | 1 | 3 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0003c0005t0003 | 0/0 | 7077 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
a0004c0006t0001 | 0/0 | 7076 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | copy fasta | chr16 | 48533726 | 48615180 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0006 | 0/1 | 3 | 0 | 1 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0014 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0005g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0008g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0008g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0008g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0009g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0011g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0011g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0012g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0012g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0015g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0016g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0017g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0018g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0019g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0020g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0021g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0022g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0023g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0024g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0025g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0026g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0001t0027g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0002t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0002t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0002t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0002t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0002t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0002t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0002t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0002t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0004t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0004t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0004t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0007t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0001c0008t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0002c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0002c0003t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0002c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0002c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0003c0005t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
a0004c0006t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0238 | EUR | GBR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0172 | EUR | GBR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | GBR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0233 | EUR | FIN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0171 | EUR | FIN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | CHS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CHS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00738 | hp2 | a0002 | c0003 | t0002 | g0284 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0154 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01070 | hp1 | a0001 | c0001 | t0008 | g0015 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01074 | hp1 | a0001 | c0001 | t0011 | g0138 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0041 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01175 | hp2 | a0001 | c0001 | t0008 | g0015 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01255 | hp1 | a0001 | c0001 | t0011 | g0139 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01255 | hp2 | a0001 | c0001 | t0008 | g0120 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01256 | hp1 | a0001 | c0001 | t0018 | g0151 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0234 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0232 | EUR | IBS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0165 | EUR | IBS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0168 | EUR | IBS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0239 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02055 | hp2 | a0001 | c0002 | t0004 | g0031 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CDX | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | CDX | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | CDX | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CDX | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02258 | hp2 | a0001 | c0002 | t0004 | g0034 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02300 | hp2 | a0001 | c0001 | t0008 | g0170 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02572 | hp2 | a0001 | c0001 | t0019 | g0044 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02602 | hp1 | a0001 | c0001 | t0017 | g0142 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0028 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02615 | hp2 | a0001 | c0001 | t0014 | g0037 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02622 | hp2 | a0001 | c0001 | t0015 | g0259 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02630 | hp1 | a0001 | c0001 | t0013 | g0036 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02630 | hp2 | a0001 | c0001 | t0009 | g0149 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02647 | hp1 | a0001 | c0002 | t0004 | g0033 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0049 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02723 | hp2 | a0001 | c0001 | t0007 | g0050 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0160 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02809 | hp1 | a0001 | c0001 | t0026 | g0098 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02886 | hp1 | a0001 | c0001 | t0025 | g0095 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0040 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02922 | hp1 | a0003 | c0005 | t0003 | g0013 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02922 | hp2 | a0001 | c0002 | t0004 | g0032 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0038 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0039 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02970 | hp2 | a0003 | c0005 | t0003 | g0013 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02976 | hp2 | a0001 | c0001 | t0022 | g0105 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0242 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03098 | hp2 | a0001 | c0004 | t0003 | g0278 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03130 | hp2 | a0001 | c0004 | t0003 | g0279 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03195 | hp2 | a0001 | c0002 | t0004 | g0008 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03225 | hp2 | a0001 | c0002 | t0004 | g0035 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0117 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03516 | hp1 | a0001 | c0002 | t0004 | g0245 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03540 | hp1 | a0001 | c0004 | t0003 | g0280 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0051 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | BEB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03834 | hp2 | a0004 | c0006 | t0001 | g0055 | SAS | BEB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | BEB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0161 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG04228 | hp2 | a0001 | c0001 | t0016 | g0143 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | YRI | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18522 | hp2 | a0001 | c0001 | t0010 | g0027 | AFR | YRI | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18906 | hp1 | a0001 | c0001 | t0021 | g0048 | AFR | YRI | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18939 | hp2 | a0002 | c0003 | t0002 | g0285 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18943 | hp2 | a0001 | c0008 | t0001 | g0282 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18971 | hp2 | a0001 | c0001 | t0027 | g0287 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18975 | hp2 | a0001 | c0001 | t0023 | g0083 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18993 | hp2 | a0001 | c0001 | t0012 | g0147 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18994 | hp1 | a0001 | c0001 | t0012 | g0145 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19011 | hp2 | a0002 | c0003 | t0002 | g0286 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19030 | hp1 | a0001 | c0007 | t0001 | g0281 | AFR | LWK | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19030 | hp2 | a0001 | c0002 | t0004 | g0030 | AFR | LWK | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0277 | AFR | LWK | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19074 | hp1 | a0002 | c0003 | t0002 | g0283 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ASW | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ASW | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0152 | EUR | TSI | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | TSI | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | GIH | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | GIH | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02109 | hp1 | a0001 | c0001 | t0024 | g0115 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0052 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02486 | hp2 | a0001 | c0002 | t0004 | g0008 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG02559 | hp2 | a0001 | c0001 | t0020 | g0090 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0150 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | USA | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | USA | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0006 | REF | REF | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0014 | REF | REF | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:48561439
|
C | A | 1 | a0004 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.1204G>T | p.Val402Leu | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/7 | 1412/7077 | 1204/2691 | 402/896 | chr16 | 48561439 | ||
chr16:48561984
|
G | T | 1 | a0003 | 2 | HG02922.hp1 HG02970.hp2 |
missense_variant | MODERATE | c.659C>A | p.Ala220Asp | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/7 | 867/7077 | 659/2691 | 220/896 | chr16 | 48561984 | ||
chr16:48609923
|
G | A | 1 | a0002 | 4 | HG00738.hp2 NA18939.hp2 NA19011.hp2 others(1): Show |
missense_variant | MODERATE | c.50C>T | p.Ala17Val | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/7 | 258/7077 | 50/2691 | 17/896 | chr16 | 48609923 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:48561005
|
T | C | 1 | a0001c0002 | 9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
synonymous_variant | LOW | c.1638A>G | p.Leu546Leu | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/7 | 1846/7077 | 1638/2691 | 546/896 | chr16 | 48561005 | ||
chr16:48609808
|
G | A | 1 | a0001c0004 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.165C>T | p.Leu55Leu | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/7 | 373/7077 | 165/2691 | 55/896 | chr16 | 48609808 | ||
chr16:48609829
|
G | A | 1 | a0001c0007 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.144C>T | p.Pro48Pro | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/7 | 352/7077 | 144/2691 | 48/896 | chr16 | 48609829 | ||
chr16:48609901
|
G | A | 1 | a0001c0008 | 1 | NA18943.hp2 | synonymous_variant | LOW | c.72C>T | p.Arg24Arg | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/7 | 280/7077 | 72/2691 | 24/896 | chr16 | 48609901 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:48538782
|
G | A | 1 | a0001c0001t0017 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4122C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 4122 | chr16 | 48538782 | |||||
chr16:48538805
|
A | G | 1 | a0001c0001t0021 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4099T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 4099 | chr16 | 48538805 | |||||
chr16:48538906
|
G | A | 18 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(15): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*3998C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3998 | chr16 | 48538906 | |||||
chr16:48539031
|
C | T | 1 | a0001c0001t0020 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3873G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3873 | chr16 | 48539031 | |||||
chr16:48539097
|
G | A | 1 | a0001c0001t0005 | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3807C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3807 | chr16 | 48539097 | |||||
chr16:48539166
|
T | C | 2 | a0001c0001t0013a0001c0001t0014 | 2 | HG02615.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3738A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3738 | chr16 | 48539166 | |||||
chr16:48539261
|
G | A | 1 | a0001c0001t0015 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3643C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3643 | chr16 | 48539261 | |||||
chr16:48539378
|
G | A | 2 | a0001c0001t0016a0001c0001t0017 | 2 | HG02602.hp1 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3526C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3526 | chr16 | 48539378 | |||||
chr16:48539515
|
C | T | 1 | a0001c0001t0008 | 4 | HG01070.hp1 HG01175.hp2 HG01255.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3389G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3389 | chr16 | 48539515 | |||||
chr16:48539517
|
A | G | 16 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(13): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*3387T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3387 | chr16 | 48539517 | |||||
chr16:48539592
|
T | C | 1 | a0001c0001t0022 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3312A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3312 | chr16 | 48539592 | |||||
chr16:48539670
|
C | T | 1 | a0001c0001t0011 | 2 | HG01074.hp1 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3234G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3234 | chr16 | 48539670 | |||||
chr16:48539806
|
G | T | 1 | a0001c0001t0010 | 2 | HG02615.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3098C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3098 | chr16 | 48539806 | |||||
chr16:48540129
|
T | G | 18 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(15): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2775A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 2775 | chr16 | 48540129 | |||||
chr16:48540175
|
T | G | 2 | a0001c0001t0006a0001c0002t0004 | 14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2729A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 2729 | chr16 | 48540175 | |||||
chr16:48540348
|
G | C | 3 | a0001c0001t0002a0001c0001t0027a0002c0003t0002 | 87 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2556C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 2556 | chr16 | 48540348 | |||||
chr16:48540358
|
G | A | 1 | a0001c0001t0023 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2546C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 2546 | chr16 | 48540358 | |||||
chr16:48540726
|
A | C | 18 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(15): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2178T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 2178 | chr16 | 48540726 | |||||
chr16:48540958
|
C | T | 14 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(11): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1946G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 1946 | chr16 | 48540958 | |||||
chr16:48541181
|
T | G | 1 | a0001c0001t0012 | 2 | NA18993.hp2 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1723A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 1723 | chr16 | 48541181 | |||||
chr16:48541320
|
G | C | 1 | a0001c0001t0024 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1584C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 1584 | chr16 | 48541320 | |||||
chr16:48541454
|
G | A | 1 | a0001c0001t0019 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1450C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 1450 | chr16 | 48541454 | |||||
chr16:48541582
|
C | T | 1 | a0001c0001t0013 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1322G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 1322 | chr16 | 48541582 | |||||
chr16:48541611
|
G | A | 1 | a0001c0001t0025 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1293C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 1293 | chr16 | 48541611 | |||||
chr16:48541967
|
G | A | 14 | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(11): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*937C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 937 | chr16 | 48541967 | |||||
chr16:48542007
|
G | A | 1 | a0001c0001t0026 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*897C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 897 | chr16 | 48542007 | |||||
chr16:48542027
|
C | T | 1 | a0001c0001t0019 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*877G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 877 | chr16 | 48542027 | |||||
chr16:48542060
|
T | A | 1 | a0001c0001t0006 | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*844A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 844 | chr16 | 48542060 | |||||
chr16:48542134
|
T | C | 2 | a0001c0001t0006a0001c0002t0004 | 14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*770A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 770 | chr16 | 48542134 | |||||
chr16:48542327
|
A | T | 1 | a0001c0001t0009 | 2 | HG02630.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*577T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 577 | chr16 | 48542327 | |||||
chr16:48542503
|
G | A | 1 | a0001c0001t0018 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*401C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 401 | chr16 | 48542503 | |||||
chr16:48542529
|
CT | C | 16 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(13): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*374delA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 374 | chr16 | 48542529 | |||||
chr16:48542890
|
G | A | 1 | a0001c0001t0007 | 5 | HG02486.hp1 HG02717.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*14C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 14 | chr16 | 48542890 | |||||
chr16:48609989
|
CGCGGCGG others(12): Show |
C | 1 | a0001c0001t0027 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-36_-18delCGGCCCCC others(11): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/7 | 18 | chr16 | 48609989 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:48543364
|
C | A | 1 | a0001c0002t0004g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2334-103G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543364 | ||||||
chr16:48543364
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2334-103G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543364 | ||||||
chr16:48543440
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2334-179C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543440 | ||||||
chr16:48543497
|
G | A | 5 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2334-236C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543497 | ||||||
chr16:48543545
|
C | A | 1 | a0001c0001t0001g0063 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2334-284G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543545 | ||||||
chr16:48543587
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.2334-326C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543587 | ||||||
chr16:48543596
|
T | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2334-335A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543596 | ||||||
chr16:48543658
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.2334-397T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543658 | ||||||
chr16:48543772
|
T | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.2334-511A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543772 | ||||||
chr16:48544034
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0020g0090 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2334-773C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48544034 | ||||||
chr16:48544065
|
C | T | 13 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(10): Show | 14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2334-804G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48544065 | ||||||
chr16:48544190
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 264 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2334-929T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48544190 | ||||||
chr16:48544920
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2333+1227C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48544920 | ||||||
chr16:48545027
|
C | T | 3 | a0001c0001t0002g0184a0001c0001t0002g0202a0001c0001t0002g0212 | 3 | HG02738.hp1 HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2333+1120G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545027 | ||||||
chr16:48545092
|
G | A | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2333+1055C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545092 | ||||||
chr16:48545111
|
C | T | 5 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0194others(2): Show | 5 | NA18973.hp1 NA18983.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.2333+1036G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545111 | ||||||
chr16:48545184
|
C | T | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2333+963G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545184 | ||||||
chr16:48545244
|
C | T | 1 | a0001c0001t0026g0098 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2333+903G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545244 | ||||||
chr16:48545295
|
C | T | 8 | a0001c0001t0002g0214a0001c0002t0004g0008a0001c0002t0004g0030others(5): Show | 9 | HG02040.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2333+852G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545295 | ||||||
chr16:48545308
|
G | A | 8 | a0001c0002t0004g0008a0001c0002t0004g0030a0001c0002t0004g0031others(5): Show | 9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2333+839C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545308 | ||||||
chr16:48545387
|
T | C | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2333+760A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545387 | ||||||
chr16:48545407
|
TA | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.2333+739delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545407 | ||||||
chr16:48545446
|
C | T | 1 | a0001c0001t0005g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2333+701G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545446 | ||||||
chr16:48545535
|
G | A | 1 | a0001c0007t0001g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2333+612C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545535 | ||||||
chr16:48545574
|
A | G | 1 | a0001c0001t0003g0162 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2333+573T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545574 | ||||||
chr16:48545893
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2333+254C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545893 | ||||||
chr16:48545899
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2333+248G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545899 | ||||||
chr16:48545915
|
T | A | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2333+232A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545915 | ||||||
chr16:48545941
|
C | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 6 | HG02622.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2333+206G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545941 | ||||||
chr16:48545967
|
G | C | 1 | a0001c0001t0003g0152 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2333+180C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545967 | ||||||
chr16:48546027
|
C | CA | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.2333+119dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48546027 | ||||||
chr16:48546039
|
A | T | 4 | a0001c0001t0003g0020a0001c0001t0003g0219a0001c0001t0003g0276others(1): Show | 5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2333+108T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48546039 | ||||||
chr16:48546040
|
A | G | 2 | a0001c0001t0016g0143a0001c0001t0017g0142 | 2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2333+107T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48546040 | ||||||
chr16:48546290
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2226-36C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546290 | ||||||
chr16:48546350
|
G | A | 1 | a0001c0001t0014g0037 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2226-96C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546350 | ||||||
chr16:48546549
|
C | G | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2226-295G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546549 | ||||||
chr16:48546623
|
G | T | 4 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0106others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2226-369C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546623 | ||||||
chr16:48546744
|
G | C | 1 | a0001c0001t0003g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2226-490C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546744 | ||||||
chr16:48546896
|
G | A | 7 | a0001c0001t0002g0175a0001c0001t0002g0177a0001c0001t0002g0178others(4): Show | 7 | HG00738.hp2 NA18939.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.2226-642C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546896 | ||||||
chr16:48546949
|
C | T | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2226-695G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546949 | ||||||
chr16:48546953
|
C | T | 1 | a0001c0001t0003g0232 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2226-699G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546953 | ||||||
chr16:48547018
|
TCAA | T | 1 | a0001c0001t0001g0005 | 3 | HG01109.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2226-767_2226-765d others(5): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48547018 | ||||||
chr16:48547217
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2225+790T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48547217 | ||||||
chr16:48547560
|
A | G | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2225+447T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48547560 | ||||||
chr16:48547737
|
A | G | 1 | a0001c0001t0003g0152 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2225+270T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48547737 | ||||||
chr16:48548508
|
C | A | 82 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(79): Show | 87 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.2118-394G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48548508 | ||||||
chr16:48548664
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2118-550A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48548664 | ||||||
chr16:48548677
|
T | C | 6 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0005g0239others(3): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2118-563A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48548677 | ||||||
chr16:48548837
|
C | CA | 19 | a0001c0001t0001g0107a0001c0001t0002g0168a0001c0001t0002g0195others(16): Show | 20 | HG01106.hp2 HG01516.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2118-724dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48548837 | ||||||
chr16:48548837
|
CA | C | 13 | a0001c0001t0001g0043a0001c0001t0001g0109a0001c0001t0002g0129others(10): Show | 15 | HG01070.hp2 HG02155.hp1 HG02273.hp1 others(12): Show |
intron_variant | MODIFIER | c.2118-724delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48548837 | ||||||
chr16:48549208
|
A | T | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2118-1094T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48549208 | ||||||
chr16:48550013
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2117+1373A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550013 | ||||||
chr16:48550066
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2117+1320G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550066 | ||||||
chr16:48550212
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2117+1174A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550212 | ||||||
chr16:48550330
|
T | C | 1 | a0001c0001t0003g0234 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2117+1056A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550330 | ||||||
chr16:48550376
|
G | A | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2117+1010C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550376 | ||||||
chr16:48550476
|
T | C | 13 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(10): Show | 14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2117+910A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550476 | ||||||
chr16:48550841
|
C | A | 7 | a0001c0002t0004g0008a0001c0002t0004g0030a0001c0002t0004g0032others(4): Show | 8 | HG02258.hp2 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2117+545G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550841 | ||||||
chr16:48550894
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2117+492G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550894 | ||||||
chr16:48551031
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.2117+355G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48551031 | ||||||
chr16:48551160
|
A | T | 1 | a0001c0001t0002g0176 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2117+226T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48551160 | ||||||
chr16:48551522
|
C | G | 8 | a0001c0002t0004g0008a0001c0002t0004g0030a0001c0002t0004g0031others(5): Show | 9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2021-40G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48551522 | ||||||
chr16:48551626
|
G | C | 1 | a0001c0001t0003g0236 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2021-144C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48551626 | ||||||
chr16:48551756
|
C | T | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2021-274G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48551756 | ||||||
chr16:48551978
|
G | A | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2021-496C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48551978 | ||||||
chr16:48552018
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2021-536T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552018 | ||||||
chr16:48552217
|
C | A | 4 | a0001c0001t0003g0020a0001c0001t0003g0219a0001c0001t0003g0276others(1): Show | 5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2021-735G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552217 | ||||||
chr16:48552426
|
G | A | 2 | a0001c0001t0010g0027a0001c0001t0010g0028 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2021-944C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552426 | ||||||
chr16:48552570
|
T | C | 2 | a0001c0001t0002g0204a0001c0001t0002g0260 | 2 | HG02074.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.2020+969A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552570 | ||||||
chr16:48552591
|
G | A | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2020+948C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552591 | ||||||
chr16:48552646
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.2020+893G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552646 | ||||||
chr16:48552684
|
C | T | 1 | a0001c0001t0010g0028 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2020+855G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552684 | ||||||
chr16:48552685
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2020+854C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552685 | ||||||
chr16:48552699
|
G | GA | 38 | a0001c0001t0001g0010a0001c0001t0001g0045a0001c0001t0001g0056others(35): Show | 39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.2020+839dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
G | GAA | 25 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0001g0058others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2020+838_2020+839d others(4): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
G | GAAA | 41 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0001g0094others(38): Show | 45 | HG00738.hp2 HG01952.hp1 HG02040.hp2 others(42): Show |
intron_variant | MODIFIER | c.2020+837_2020+839d others(5): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
G | GAAAA | 35 | a0001c0001t0001g0063a0001c0001t0001g0086a0001c0001t0001g0099others(32): Show | 37 | HG01258.hp1 HG01934.hp1 HG01993.hp1 others(34): Show |
intron_variant | MODIFIER | c.2020+836_2020+839d others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
G | GAAAAA | 10 | a0001c0001t0001g0114a0001c0001t0002g0191a0001c0001t0002g0205others(7): Show | 11 | HG00621.hp2 HG01346.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2020+835_2020+839d others(7): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
G | GAAAAAAA others(2): Show |
7 | a0001c0001t0002g0019a0001c0001t0002g0128a0001c0001t0002g0134others(4): Show | 8 | HG00639.hp1 HG01243.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.2020+831_2020+839d others(11): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
G | GAAAAAAA others(3): Show |
2 | a0001c0001t0001g0102a0001c0001t0002g0206 | 2 | HG01433.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2020+830_2020+839d others(12): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
G | GAAAAAAA others(4): Show |
1 | a0001c0001t0002g0212 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2020+829_2020+839d others(13): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
G | GAAAAAAA others(5): Show |
1 | a0001c0001t0005g0240 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2020+828_2020+839d others(14): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
G | GAAAAAAA others(6): Show |
1 | a0001c0001t0002g0183 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2020+827_2020+839d others(15): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
G | GAAAAAAA others(10): Show |
1 | a0001c0001t0001g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2020+823_2020+839d others(19): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
G | GAAAAAAA others(12): Show |
2 | a0001c0001t0002g0188a0001c0001t0020g0090 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2020+821_2020+839d others(21): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
GA | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(24): Show | 39 | HG00673.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.2020+839delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
GAAAAAAA others(6): Show |
G | 5 | a0001c0001t0001g0068a0001c0001t0002g0209a0001c0001t0013g0036others(2): Show | 5 | HG02273.hp2 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2020+827_2020+839d others(15): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
GAAAAAAA others(7): Show |
G | 10 | a0001c0001t0001g0053a0001c0001t0001g0092a0001c0001t0002g0122others(7): Show | 11 | HG02258.hp2 HG02486.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2020+826_2020+839d others(16): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
GAAAAAAA others(9): Show |
G | 3 | a0001c0001t0001g0088a0001c0001t0001g0100a0003c0005t0003g0013 | 4 | HG01123.hp1 HG01169.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2020+824_2020+839d others(18): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
GAAAAAAA others(11): Show |
G | 1 | a0001c0001t0002g0168 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2020+822_2020+839d others(20): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
GAAAAAAA others(14): Show |
G | 1 | a0001c0001t0002g0201 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2020+819_2020+839d others(23): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
GAAAAAAA others(16): Show |
G | 1 | a0001c0001t0001g0005 | 3 | HG01109.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2020+817_2020+839d others(25): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552699
|
GAAAAAAA others(18): Show |
G | 1 | a0001c0001t0003g0152 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2020+815_2020+839d others(27): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | ||||||
chr16:48552713
|
A | G | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2020+826T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552713 | ||||||
chr16:48552899
|
C | T | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.2020+640G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552899 | ||||||
chr16:48553151
|
T | C | 3 | a0001c0001t0001g0262a0001c0001t0001g0267a0001c0001t0001g0268 | 3 | HG03017.hp2 HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2020+388A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48553151 | ||||||
chr16:48553172
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.2020+367A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48553172 | ||||||
chr16:48553310
|
A | G | 7 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0063others(4): Show | 7 | HG01993.hp1 HG03239.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.2020+229T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48553310 | ||||||
chr16:48553968
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0047others(11): Show | 17 | HG00323.hp1 HG00741.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1890-299C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48553968 | ||||||
chr16:48554173
|
TA | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1890-505delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554173 | ||||||
chr16:48554320
|
G | A | 2 | a0001c0001t0009g0149a0001c0001t0009g0150 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1890-651C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554320 | ||||||
chr16:48554369
|
G | A | 1 | a0001c0002t0004g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1890-700C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554369 | ||||||
chr16:48554369
|
G | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0271 | 2 | NA18973.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1890-700C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554369 | ||||||
chr16:48554553
|
A | G | 1 | a0001c0001t0002g0248 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1890-884T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554553 | ||||||
chr16:48554610
|
T | C | 2 | a0001c0001t0003g0258a0001c0001t0015g0259 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1890-941A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554610 | ||||||
chr16:48554703
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 263 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1890-1034A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554703 | ||||||
chr16:48554710
|
T | C | 1 | a0001c0001t0001g0009 | 2 | NA19074.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1890-1041A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554710 | ||||||
chr16:48555135
|
G | A | 1 | a0001c0001t0016g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1890-1466C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555135 | ||||||
chr16:48555141
|
T | C | 1 | a0001c0001t0002g0250 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1890-1472A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555141 | ||||||
chr16:48555151
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 263 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1890-1482A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555151 | ||||||
chr16:48555158
|
T | C | 1 | a0001c0002t0004g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1890-1489A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555158 | ||||||
chr16:48555280
|
A | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0112others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890-1611T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555280 | ||||||
chr16:48555450
|
A | T | 1 | a0001c0004t0003g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1890-1781T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555450 | ||||||
chr16:48555731
|
AG | A | 8 | a0001c0002t0004g0008a0001c0002t0004g0030a0001c0002t0004g0031others(5): Show | 9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1890-2063delC | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555731 | ||||||
chr16:48555962
|
G | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1890-2293C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555962 | ||||||
chr16:48555985
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1890-2316C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555985 | ||||||
chr16:48556044
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1890-2375C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556044 | ||||||
chr16:48556234
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1890-2565T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556234 | ||||||
chr16:48556313
|
C | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0106others(2): Show | 5 | HG02572.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1890-2644G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556313 | ||||||
chr16:48556416
|
G | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(12): Show | 19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1890-2747C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556416 | ||||||
chr16:48556561
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0047others(11): Show | 17 | HG00323.hp1 HG00741.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1890-2892C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556561 | ||||||
chr16:48556578
|
G | T | 1 | a0001c0001t0002g0210 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1890-2909C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556578 | ||||||
chr16:48556677
|
G | A | 7 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0063others(4): Show | 7 | HG01993.hp1 HG03239.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1890-3008C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556677 | ||||||
chr16:48556716
|
A | T | 5 | a0001c0001t0002g0016a0001c0001t0002g0124a0001c0001t0002g0136others(2): Show | 6 | NA18945.hp1 NA18952.hp2 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.1890-3047T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556716 | ||||||
chr16:48556745
|
G | A | 1 | a0001c0001t0016g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1890-3076C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556745 | ||||||
chr16:48556788
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1890-3119G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556788 | ||||||
chr16:48556889
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1890-3220T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556889 | ||||||
chr16:48556907
|
A | G | 1 | a0001c0001t0003g0155 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1890-3238T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556907 | ||||||
chr16:48557101
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1890-3432A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48557101 | ||||||
chr16:48557690
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1889+3064G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48557690 | ||||||
chr16:48557708
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1889+3046A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48557708 | ||||||
chr16:48557727
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+3027A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48557727 | ||||||
chr16:48557806
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1889+2948T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48557806 | ||||||
chr16:48557837
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1889+2917C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48557837 | ||||||
chr16:48558293
|
C | CA | 6 | a0001c0001t0001g0100a0001c0001t0002g0188a0001c0001t0002g0207others(3): Show | 6 | HG00741.hp2 HG01106.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1889+2460dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558293 | ||||||
chr16:48558293
|
CA | C | 31 | a0001c0001t0001g0067a0001c0001t0001g0109a0001c0001t0001g0264others(28): Show | 33 | HG01070.hp2 HG01106.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.1889+2460delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558293 | ||||||
chr16:48558317
|
TA | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+2436delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558317 | ||||||
chr16:48558448
|
T | C | 1 | a0003c0005t0003g0013 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1889+2306A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558448 | ||||||
chr16:48558465
|
G | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+2289C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558465 | ||||||
chr16:48558665
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1889+2089A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558665 | ||||||
chr16:48558797
|
G | A | 4 | a0001c0001t0003g0020a0001c0001t0003g0219a0001c0001t0003g0276others(1): Show | 5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1889+1957C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558797 | ||||||
chr16:48558931
|
AATG | A | 5 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1889+1820_1889+182 others(7): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558931 | ||||||
chr16:48559154
|
C | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+1600G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559154 | ||||||
chr16:48559164
|
ATTATC | A | 6 | a0001c0001t0002g0134a0001c0001t0002g0186a0001c0001t0002g0187others(3): Show | 6 | NA18941.hp2 NA18957.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.1889+1585_1889+158 others(9): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559164 | ||||||
chr16:48559387
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+1367A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559387 | ||||||
chr16:48559476
|
A | C | 1 | a0001c0001t0006g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1889+1278T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559476 | ||||||
chr16:48559722
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1889+1032G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559722 | ||||||
chr16:48559732
|
A | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+1022T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559732 | ||||||
chr16:48559781
|
C | T | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1889+973G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559781 | ||||||
chr16:48559868
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+886T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559868 | ||||||
chr16:48560103
|
G | GA | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1889+650dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560103 | ||||||
chr16:48560310
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+444T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560310 | ||||||
chr16:48560318
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1889+436G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560318 | ||||||
chr16:48560334
|
A | T | 1 | a0001c0001t0001g0108 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1889+420T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560334 | ||||||
chr16:48560376
|
TA | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+377delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560376 | ||||||
chr16:48560456
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1889+298T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560456 | ||||||
chr16:48560500
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1889+254C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560500 | ||||||
chr16:48560602
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0100 | 2 | HG01123.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1889+152T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560602 | ||||||
chr16:48562577
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199-133C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48562577 | ||||||
chr16:48562699
|
G | C | 1 | a0001c0001t0003g0165 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.199-255C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48562699 | ||||||
chr16:48562842
|
G | A | 1 | a0001c0001t0018g0151 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.199-398C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48562842 | ||||||
chr16:48562984
|
A | AT | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-541dupA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48562984 | ||||||
chr16:48563081
|
G | C | 1 | a0001c0001t0003g0157 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.199-637C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563081 | ||||||
chr16:48563110
|
T | C | 1 | a0003c0005t0003g0013 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-666A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563110 | ||||||
chr16:48563141
|
T | A | 4 | a0001c0001t0001g0087a0001c0001t0002g0122a0001c0001t0002g0208others(1): Show | 4 | NA18906.hp2 NA18942.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-697A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563141 | ||||||
chr16:48563175
|
C | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0264others(1): Show | 6 | NA18947.hp1 NA18953.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-731G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563175 | ||||||
chr16:48563249
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.199-805C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563249 | ||||||
chr16:48563341
|
C | T | 3 | a0001c0001t0008g0015a0001c0001t0008g0120a0001c0001t0008g0170 | 4 | HG01070.hp1 HG01175.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-897G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563341 | ||||||
chr16:48563342
|
G | A | 1 | a0001c0001t0003g0020 | 2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.199-898C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563342 | ||||||
chr16:48563347
|
C | G | 5 | a0001c0001t0003g0020a0001c0001t0003g0219a0001c0001t0003g0276others(2): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-903G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563347 | ||||||
chr16:48563364
|
A | T | 8 | a0001c0002t0004g0008a0001c0002t0004g0030a0001c0002t0004g0031others(5): Show | 9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-920T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563364 | ||||||
chr16:48563447
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.199-1003T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563447 | ||||||
chr16:48563757
|
G | C | 1 | a0001c0001t0002g0196 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.199-1313C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563757 | ||||||
chr16:48563815
|
G | A | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-1371C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563815 | ||||||
chr16:48564004
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-1560C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564004 | ||||||
chr16:48564109
|
C | G | 1 | a0001c0001t0006g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.199-1665G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564109 | ||||||
chr16:48564153
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-1709T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564153 | ||||||
chr16:48564463
|
T | C | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-2019A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564463 | ||||||
chr16:48564606
|
C | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-2162G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564606 | ||||||
chr16:48564704
|
G | A | 3 | a0001c0001t0003g0144a0001c0001t0003g0154a0001c0001t0003g0161 | 3 | HG00741.hp2 HG01106.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.199-2260C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564704 | ||||||
chr16:48564782
|
C | A | 1 | a0001c0001t0002g0191 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.199-2338G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564782 | ||||||
chr16:48564826
|
T | A | 8 | a0001c0001t0002g0133a0001c0001t0002g0191a0001c0001t0002g0197others(5): Show | 8 | HG00621.hp2 HG02132.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.199-2382A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564826 | ||||||
chr16:48564826
|
T | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-2382A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564826 | ||||||
chr16:48564878
|
C | A | 4 | a0001c0001t0003g0020a0001c0001t0003g0219a0001c0001t0003g0276others(1): Show | 5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-2434G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564878 | ||||||
chr16:48564973
|
A | G | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.199-2529T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564973 | ||||||
chr16:48565073
|
G | A | 1 | a0001c0001t0015g0259 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.199-2629C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48565073 | ||||||
chr16:48565539
|
T | C | 2 | a0001c0001t0003g0276a0001c0001t0003g0277 | 2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.199-3095A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48565539 | ||||||
chr16:48565619
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(99): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.199-3175T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48565619 | ||||||
chr16:48565698
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-3254A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48565698 | ||||||
chr16:48565906
|
T | C | 20 | a0001c0001t0003g0006a0001c0001t0003g0144a0001c0001t0003g0152others(17): Show | 22 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.199-3462A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48565906 | ||||||
chr16:48565980
|
T | C | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.199-3536A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48565980 | ||||||
chr16:48566085
|
T | C | 1 | a0001c0001t0003g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.199-3641A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48566085 | ||||||
chr16:48566397
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.199-3953C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48566397 | ||||||
chr16:48566421
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-3977C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48566421 | ||||||
chr16:48566465
|
C | T | 8 | a0001c0002t0004g0008a0001c0002t0004g0030a0001c0002t0004g0031others(5): Show | 9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-4021G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48566465 | ||||||
chr16:48567377
|
C | T | 1 | a0003c0005t0003g0013 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-4933G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567377 | ||||||
chr16:48567380
|
A | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.199-4936T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567380 | ||||||
chr16:48567410
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-4966A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567410 | ||||||
chr16:48567433
|
T | C | 1 | a0001c0001t0003g0164 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.199-4989A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567433 | ||||||
chr16:48567449
|
C | T | 2 | a0001c0001t0012g0145a0001c0001t0012g0147 | 2 | NA18993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.199-5005G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567449 | ||||||
chr16:48567610
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-5166A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567610 | ||||||
chr16:48567615
|
G | A | 1 | a0001c0001t0003g0229 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.199-5171C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567615 | ||||||
chr16:48567627
|
A | C | 5 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-5183T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567627 | ||||||
chr16:48567739
|
CTTATA | C | 2 | a0001c0001t0005g0022a0001c0001t0005g0023 | 4 | HG02451.hp1 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-5300_199-5296d others(7): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567739 | ||||||
chr16:48568198
|
T | C | 1 | a0001c0001t0006g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.199-5754A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568198 | ||||||
chr16:48568229
|
C | T | 13 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(10): Show | 14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-5785G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568229 | ||||||
chr16:48568332
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-5888C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568332 | ||||||
chr16:48568348
|
T | C | 1 | a0001c0001t0002g0187 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.199-5904A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568348 | ||||||
chr16:48568684
|
C | A | 1 | a0001c0001t0003g0159 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.199-6240G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568684 | ||||||
chr16:48568767
|
ATTG | A | 8 | a0001c0002t0004g0008a0001c0002t0004g0030a0001c0002t0004g0031others(5): Show | 9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-6326_199-6324d others(5): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568767 | ||||||
chr16:48568812
|
A | G | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.199-6368T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568812 | ||||||
chr16:48568822
|
C | T | 101 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(98): Show | 109 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(106): Show |
intron_variant | MODIFIER | c.199-6378G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568822 | ||||||
chr16:48568850
|
G | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-6406C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568850 | ||||||
chr16:48569092
|
C | T | 19 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(16): Show | 22 | HG00673.hp1 HG01952.hp2 HG03017.hp2 others(19): Show |
intron_variant | MODIFIER | c.199-6648G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569092 | ||||||
chr16:48569163
|
A | G | 1 | a0003c0005t0003g0013 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-6719T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569163 | ||||||
chr16:48569187
|
C | T | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.199-6743G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569187 | ||||||
chr16:48569256
|
TG | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0056a0004c0006t0001g0055 | 3 | HG03239.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.199-6813delC | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569256 | ||||||
chr16:48569281
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-6837G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569281 | ||||||
chr16:48569415
|
AG | A | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-6972delC | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569415 | ||||||
chr16:48569455
|
C | T | 1 | a0001c0001t0026g0098 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.199-7011G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569455 | ||||||
chr16:48569591
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(78): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.199-7147G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569591 | ||||||
chr16:48569822
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0272 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.199-7378G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569822 | ||||||
chr16:48569853
|
T | C | 4 | a0001c0001t0003g0020a0001c0001t0003g0219a0001c0001t0003g0276others(1): Show | 5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-7409A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569853 | ||||||
chr16:48569860
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.199-7416G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569860 | ||||||
chr16:48570185
|
C | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.199-7741G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570185 | ||||||
chr16:48570270
|
G | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0219 | 3 | HG02451.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.199-7826C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570270 | ||||||
chr16:48570279
|
G | A | 1 | a0001c0001t0002g0175 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.199-7835C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570279 | ||||||
chr16:48570369
|
G | A | 1 | a0001c0001t0003g0180 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.199-7925C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570369 | ||||||
chr16:48570611
|
C | T | 8 | a0001c0002t0004g0008a0001c0002t0004g0030a0001c0002t0004g0031others(5): Show | 9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-8167G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570611 | ||||||
chr16:48570863
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.199-8419G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570863 | ||||||
chr16:48570951
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-8507C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570951 | ||||||
chr16:48571055
|
G | A | 1 | a0003c0005t0003g0013 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-8611C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571055 | ||||||
chr16:48571109
|
C | T | 2 | a0001c0001t0016g0143a0001c0001t0017g0142 | 2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.199-8665G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571109 | ||||||
chr16:48571235
|
A | T | 4 | a0001c0001t0003g0217a0001c0001t0003g0243a0001c0001t0003g0244others(1): Show | 4 | HG03041.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-8791T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571235 | ||||||
chr16:48571236
|
A | G | 4 | a0001c0001t0003g0217a0001c0001t0003g0243a0001c0001t0003g0244others(1): Show | 4 | HG03041.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-8792T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571236 | ||||||
chr16:48571254
|
C | T | 1 | a0001c0001t0013g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.199-8810G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571254 | ||||||
chr16:48571551
|
C | T | 7 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0003g0255others(4): Show | 7 | HG00738.hp2 NA18939.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-9107G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571551 | ||||||
chr16:48571687
|
C | A | 5 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-9243G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571687 | ||||||
chr16:48572073
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.199-9629C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572073 | ||||||
chr16:48572166
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-9722G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572166 | ||||||
chr16:48572180
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-9736A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572180 | ||||||
chr16:48572445
|
C | T | 1 | a0001c0001t0002g0247 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.199-10001G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572445 | ||||||
chr16:48572518
|
G | A | 6 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0003g0232others(3): Show | 6 | HG00280.hp1 HG00738.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-10074C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572518 | ||||||
chr16:48572552
|
T | C | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-10108A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572552 | ||||||
chr16:48572587
|
A | C | 1 | a0001c0001t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.199-10143T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572587 | ||||||
chr16:48572746
|
T | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.199-10302A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572746 | ||||||
chr16:48572819
|
A | G | 1 | a0003c0005t0003g0013 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-10375T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572819 | ||||||
chr16:48573108
|
CA | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(109): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.199-10665delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48573108 | ||||||
chr16:48573170
|
C | T | 1 | a0001c0001t0002g0247 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.199-10726G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48573170 | ||||||
chr16:48573185
|
C | T | 2 | a0001c0001t0010g0027a0001c0001t0010g0028 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.199-10741G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48573185 | ||||||
chr16:48573318
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-10874T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48573318 | ||||||
chr16:48573482
|
A | T | 1 | a0001c0001t0019g0044 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.199-11038T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48573482 | ||||||
chr16:48573891
|
T | C | 1 | a0001c0001t0007g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.199-11447A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48573891 | ||||||
chr16:48574055
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-11611A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574055 | ||||||
chr16:48574062
|
T | C | 1 | a0001c0001t0002g0212 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.199-11618A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574062 | ||||||
chr16:48574169
|
A | G | 3 | a0001c0001t0001g0262a0001c0001t0001g0267a0001c0001t0001g0268 | 3 | HG03017.hp2 HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.199-11725T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574169 | ||||||
chr16:48574252
|
A | T | 1 | a0001c0001t0002g0198 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.199-11808T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574252 | ||||||
chr16:48574345
|
T | G | 5 | a0001c0001t0002g0119a0001c0001t0002g0125a0001c0001t0002g0126others(2): Show | 5 | HG01934.hp1 HG02083.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-11901A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574345 | ||||||
chr16:48574377
|
T | C | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-11933A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574377 | ||||||
chr16:48574444
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.199-12000A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574444 | ||||||
chr16:48574608
|
G | A | 5 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-12164C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574608 | ||||||
chr16:48574748
|
C | G | 1 | a0001c0001t0003g0218 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-12304G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574748 | ||||||
chr16:48575244
|
A | C | 104 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(101): Show | 112 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(109): Show |
intron_variant | MODIFIER | c.199-12800T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48575244 | ||||||
chr16:48575484
|
C | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(36): Show | 53 | HG00140.hp2 HG00639.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.199-13040G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48575484 | ||||||
chr16:48575559
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.199-13115C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48575559 | ||||||
chr16:48575646
|
A | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 4 | HG00323.hp1 HG03704.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-13202T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48575646 | ||||||
chr16:48575748
|
A | G | 3 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182 | 3 | HG01074.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.199-13304T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48575748 | ||||||
chr16:48575919
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.199-13475G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48575919 | ||||||
chr16:48576381
|
G | A | 1 | a0001c0001t0011g0139 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.199-13937C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48576381 | ||||||
chr16:48576861
|
T | C | 1 | a0001c0001t0002g0213 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.199-14417A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48576861 | ||||||
chr16:48576900
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.199-14456A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48576900 | ||||||
chr16:48576953
|
C | G | 17 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0054others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.199-14509G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48576953 | ||||||
chr16:48577022
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-14578A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577022 | ||||||
chr16:48577129
|
C | T | 1 | a0001c0001t0013g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.199-14685G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577129 | ||||||
chr16:48577315
|
G | GT | 6 | a0001c0001t0001g0272a0001c0001t0002g0121a0001c0001t0016g0143others(3): Show | 6 | HG03098.hp2 HG03130.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-14872dupA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577315 | ||||||
chr16:48577315
|
G | GTT | 6 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0005g0239others(3): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-14873_199-1487 others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577315 | ||||||
chr16:48577394
|
T | A | 2 | a0001c0001t0002g0225a0001c0001t0002g0252 | 2 | NA18974.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.199-14950A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577394 | ||||||
chr16:48577647
|
G | A | 1 | a0001c0001t0003g0229 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.199-15203C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577647 | ||||||
chr16:48577825
|
C | T | 2 | a0001c0001t0003g0020a0001c0001t0003g0219 | 3 | HG02451.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.199-15381G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577825 | ||||||
chr16:48577992
|
G | A | 1 | a0001c0001t0006g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.199-15548C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577992 | ||||||
chr16:48577997
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.199-15553G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577997 | ||||||
chr16:48577998
|
G | A | 21 | a0001c0001t0002g0175a0001c0001t0003g0007a0001c0001t0003g0135others(18): Show | 23 | HG00621.hp1 HG01069.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-15554C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577998 | ||||||
chr16:48578450
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-16006T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48578450 | ||||||
chr16:48578497
|
C | T | 5 | a0001c0001t0002g0119a0001c0001t0002g0125a0001c0001t0002g0126others(2): Show | 5 | HG01934.hp1 HG02083.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-16053G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48578497 | ||||||
chr16:48578692
|
C | T | 1 | a0001c0001t0002g0196 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.199-16248G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48578692 | ||||||
chr16:48578996
|
GCATTTGA others(13): Show |
G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-16572_199-1655 others(24): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48578996 | ||||||
chr16:48579039
|
T | C | 6 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(3): Show | 6 | HG01106.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-16595A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579039 | ||||||
chr16:48579173
|
G | A | 1 | a0001c0001t0002g0175 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.199-16729C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579173 | ||||||
chr16:48579338
|
T | A | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-16894A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579338 | ||||||
chr16:48579410
|
C | G | 1 | a0001c0001t0003g0276 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.199-16966G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579410 | ||||||
chr16:48579427
|
A | T | 1 | a0001c0001t0001g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.199-16983T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579427 | ||||||
chr16:48579911
|
T | A | 1 | a0001c0002t0004g0033 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.199-17467A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579911 | ||||||
chr16:48579926
|
CAT | C | 7 | a0001c0001t0001g0084a0001c0001t0006g0038a0001c0001t0006g0039others(4): Show | 7 | HG01106.hp2 HG01891.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-17484_199-1748 others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579926 | ||||||
chr16:48580039
|
A | C | 1 | a0001c0001t0001g0093 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.199-17595T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580039 | ||||||
chr16:48580168
|
T | C | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.199-17724A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580168 | ||||||
chr16:48580172
|
G | A | 13 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(10): Show | 14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-17728C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580172 | ||||||
chr16:48580312
|
C | T | 13 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(10): Show | 14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-17868G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580312 | ||||||
chr16:48580382
|
G | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-17938C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580382 | ||||||
chr16:48580752
|
C | A | 5 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-18308G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580752 | ||||||
chr16:48580794
|
T | C | 19 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(16): Show | 22 | HG00673.hp1 HG01952.hp2 HG03017.hp2 others(19): Show |
intron_variant | MODIFIER | c.199-18350A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580794 | ||||||
chr16:48580926
|
A | G | 1 | a0001c0001t0002g0195 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.199-18482T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580926 | ||||||
chr16:48580935
|
G | A | 3 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0005g0242 | 5 | HG02451.hp1 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-18491C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580935 | ||||||
chr16:48581136
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.199-18692A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48581136 | ||||||
chr16:48581248
|
T | TA | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.199-18805dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48581248 | ||||||
chr16:48581375
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.199-18931G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48581375 | ||||||
chr16:48581812
|
A | G | 4 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0194others(1): Show | 4 | NA18983.hp2 NA18988.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-19368T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48581812 | ||||||
chr16:48581897
|
A | C | 1 | a0001c0001t0001g0064 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.199-19453T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48581897 | ||||||
chr16:48582220
|
C | A | 2 | a0001c0001t0009g0149a0001c0001t0009g0150 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.199-19776G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582220 | ||||||
chr16:48582367
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-19923C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582367 | ||||||
chr16:48582458
|
T | TA | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-20015dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582458 | ||||||
chr16:48582694
|
GA | G | 4 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0106others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-20251delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582694 | ||||||
chr16:48582722
|
G | A | 4 | a0001c0001t0002g0247a0001c0001t0002g0249a0001c0001t0002g0250others(1): Show | 4 | HG02523.hp1 NA18949.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-20278C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582722 | ||||||
chr16:48582782
|
G | C | 1 | a0001c0001t0001g0063 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.199-20338C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582782 | ||||||
chr16:48582878
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-20434T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582878 | ||||||
chr16:48582946
|
T | A | 1 | a0001c0001t0001g0077 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.199-20502A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582946 | ||||||
chr16:48583065
|
G | A | 13 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(10): Show | 14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-20621C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583065 | ||||||
chr16:48583151
|
C | T | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-20707G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583151 | ||||||
chr16:48583413
|
T | A | 4 | a0001c0001t0003g0020a0001c0001t0003g0219a0001c0001t0003g0276others(1): Show | 5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-20969A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583413 | ||||||
chr16:48583421
|
A | C | 4 | a0001c0001t0003g0020a0001c0001t0003g0219a0001c0001t0003g0276others(1): Show | 5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-20977T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583421 | ||||||
chr16:48583636
|
T | A | 2 | a0001c0001t0010g0027a0001c0001t0010g0028 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.199-21192A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583636 | ||||||
chr16:48583699
|
T | C | 6 | a0001c0001t0001g0053a0001c0001t0001g0089a0001c0001t0001g0091others(3): Show | 6 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-21255A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583699 | ||||||
chr16:48583843
|
T | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-21399A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583843 | ||||||
chr16:48583871
|
T | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(117): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.199-21427A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583871 | ||||||
chr16:48583939
|
G | A | 1 | a0001c0001t0010g0027 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.199-21495C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583939 | ||||||
chr16:48584457
|
T | G | 1 | a0001c0001t0003g0148 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.199-22013A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48584457 | ||||||
chr16:48584610
|
C | CAA | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-22168_199-2216 others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48584610 | ||||||
chr16:48584662
|
C | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-22218G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48584662 | ||||||
chr16:48584827
|
T | G | 3 | a0001c0001t0003g0217a0001c0001t0003g0243a0001c0001t0003g0244 | 3 | HG03041.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.199-22383A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48584827 | ||||||
chr16:48584867
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.199-22423A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48584867 | ||||||
chr16:48585183
|
T | A | 2 | a0001c0001t0003g0258a0001c0001t0015g0259 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.199-22739A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585183 | ||||||
chr16:48585202
|
G | A | 1 | a0001c0001t0003g0160 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.199-22758C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585202 | ||||||
chr16:48585262
|
A | G | 1 | a0001c0001t0003g0217 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.199-22818T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585262 | ||||||
chr16:48585397
|
G | A | 7 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0109others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-22953C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585397 | ||||||
chr16:48585413
|
G | A | 1 | a0001c0001t0002g0221 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.199-22969C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585413 | ||||||
chr16:48585415
|
T | C | 2 | a0001c0001t0010g0027a0001c0001t0010g0028 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.199-22971A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585415 | ||||||
chr16:48585462
|
C | A | 1 | a0001c0001t0003g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.199-23018G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585462 | ||||||
chr16:48585608
|
G | A | 1 | a0001c0001t0003g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.199-23164C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585608 | ||||||
chr16:48585702
|
C | CT | 7 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0106others(4): Show | 7 | HG00621.hp2 HG02818.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-23259dupA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585702 | ||||||
chr16:48585916
|
C | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(112): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.199-23472G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585916 | ||||||
chr16:48586030
|
G | A | 85 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(82): Show | 90 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.199-23586C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586030 | ||||||
chr16:48586292
|
G | A | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+23483C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586292 | ||||||
chr16:48586454
|
A | G | 1 | a0001c0001t0019g0044 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.198+23321T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586454 | ||||||
chr16:48586484
|
C | T | 2 | a0001c0001t0010g0027a0001c0001t0010g0028 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.198+23291G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586484 | ||||||
chr16:48586598
|
G | A | 6 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0005g0239others(3): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+23177C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586598 | ||||||
chr16:48586603
|
A | C | 1 | a0001c0001t0013g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.198+23172T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586603 | ||||||
chr16:48586867
|
A | T | 2 | a0001c0001t0009g0149a0001c0001t0009g0150 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.198+22908T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586867 | ||||||
chr16:48586869
|
A | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+22906T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586869 | ||||||
chr16:48586921
|
C | T | 1 | a0003c0005t0003g0013 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198+22854G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586921 | ||||||
chr16:48586987
|
G | A | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+22788C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586987 | ||||||
chr16:48587053
|
C | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+22722G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587053 | ||||||
chr16:48587059
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.198+22716T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587059 | ||||||
chr16:48587141
|
T | A | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+22634A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587141 | ||||||
chr16:48587260
|
T | G | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+22515A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587260 | ||||||
chr16:48587286
|
T | C | 1 | a0001c0001t0002g0222 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.198+22489A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587286 | ||||||
chr16:48587301
|
G | A | 1 | a0001c0001t0003g0166 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.198+22474C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587301 | ||||||
chr16:48587433
|
A | G | 1 | a0003c0005t0003g0013 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198+22342T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587433 | ||||||
chr16:48587491
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+22284A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587491 | ||||||
chr16:48587561
|
C | T | 7 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0109others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+22214G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587561 | ||||||
chr16:48587800
|
A | G | 1 | a0001c0001t0002g0190 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.198+21975T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587800 | ||||||
chr16:48587909
|
G | A | 2 | a0001c0001t0001g0054a0004c0006t0001g0055 | 2 | HG03239.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.198+21866C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587909 | ||||||
chr16:48587963
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.198+21812A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587963 | ||||||
chr16:48588215
|
A | G | 1 | a0001c0001t0013g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.198+21560T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588215 | ||||||
chr16:48588246
|
AAGGTAAA others(4226): Show |
A | 1 | a0001c0001t0021g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.198+17296_198+2152 others(4): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588246 | ||||||
chr16:48588294
|
CT | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.198+21480delA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588294 | ||||||
chr16:48588333
|
C | T | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+21442G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588333 | ||||||
chr16:48588370
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.198+21405A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588370 | ||||||
chr16:48588389
|
G | A | 3 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0005g0242 | 5 | HG02451.hp1 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+21386C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588389 | ||||||
chr16:48588440
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.198+21335T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588440 | ||||||
chr16:48588483
|
C | T | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+21292G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588483 | ||||||
chr16:48588671
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.198+21104A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588671 | ||||||
chr16:48588672
|
C | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.198+21103G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588672 | ||||||
chr16:48588842
|
C | T | 1 | a0001c0001t0002g0189 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.198+20933G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588842 | ||||||
chr16:48589020
|
A | G | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+20755T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589020 | ||||||
chr16:48589267
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.198+20508C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589267 | ||||||
chr16:48589284
|
G | A | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+20491C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589284 | ||||||
chr16:48589306
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.198+20469A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589306 | ||||||
chr16:48589315
|
C | T | 7 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0109others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+20460G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589315 | ||||||
chr16:48589316
|
T | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.198+20459A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589316 | ||||||
chr16:48589411
|
G | T | 1 | a0001c0001t0002g0188 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.198+20364C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589411 | ||||||
chr16:48589436
|
T | A | 1 | a0001c0001t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.198+20339A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589436 | ||||||
chr16:48589536
|
A | G | 1 | a0003c0005t0003g0013 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198+20239T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589536 | ||||||
chr16:48589628
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.198+20147G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589628 | ||||||
chr16:48589710
|
T | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.198+20065A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589710 | ||||||
chr16:48589863
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.198+19912C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589863 | ||||||
chr16:48589884
|
G | A | 1 | a0001c0001t0026g0098 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.198+19891C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589884 | ||||||
chr16:48589917
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0101 | 3 | HG02622.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.198+19858A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589917 | ||||||
chr16:48589953
|
G | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(35): Show | 52 | HG00140.hp2 HG00639.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.198+19822C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589953 | ||||||
chr16:48590084
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.198+19691G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590084 | ||||||
chr16:48590153
|
A | G | 1 | a0001c0001t0010g0027 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.198+19622T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590153 | ||||||
chr16:48590173
|
C | A | 1 | a0001c0001t0026g0098 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.198+19602G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590173 | ||||||
chr16:48590340
|
C | T | 8 | a0001c0002t0004g0008a0001c0002t0004g0030a0001c0002t0004g0031others(5): Show | 9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+19435G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590340 | ||||||
chr16:48590486
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.198+19289C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590486 | ||||||
chr16:48590510
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0101 | 3 | HG02622.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.198+19265C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590510 | ||||||
chr16:48590551
|
C | T | 6 | a0001c0001t0001g0053a0001c0001t0001g0089a0001c0001t0001g0091others(3): Show | 6 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+19224G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590551 | ||||||
chr16:48590634
|
G | A | 13 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(10): Show | 14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+19141C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590634 | ||||||
chr16:48590893
|
CTTAG | C | 19 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(16): Show | 22 | HG00673.hp1 HG01952.hp2 HG03017.hp2 others(19): Show |
intron_variant | MODIFIER | c.198+18878_198+1888 others(8): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590893 | ||||||
chr16:48591036
|
G | C | 1 | a0001c0001t0003g0162 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.198+18739C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591036 | ||||||
chr16:48591101
|
G | C | 3 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0005g0242 | 5 | HG02451.hp1 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+18674C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591101 | ||||||
chr16:48591547
|
A | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.198+18228T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591547 | ||||||
chr16:48591632
|
GT | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.198+18142delA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591632 | ||||||
chr16:48591741
|
A | T | 1 | a0001c0001t0001g0060 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.198+18034T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591741 | ||||||
chr16:48591832
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.198+17943A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591832 | ||||||
chr16:48591885
|
CG | C | 3 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0003g0238 | 3 | HG00099.hp2 HG01109.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.198+17889delC | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591885 | ||||||
chr16:48591886
|
G | GT | 102 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(99): Show | 110 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(107): Show |
intron_variant | MODIFIER | c.198+17888dupA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591886 | ||||||
chr16:48591886
|
G | GTT | 8 | a0001c0001t0002g0121a0001c0001t0002g0185a0001c0001t0002g0186others(5): Show | 9 | HG02148.hp1 HG02451.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+17887_198+1788 others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591886 | ||||||
chr16:48591886
|
G | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0266 | 2 | HG01952.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.198+17889C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591886 | ||||||
chr16:48591898
|
T | TTTC | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(112): Show | 137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.198+17876_198+1787 others(7): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591898 | ||||||
chr16:48591993
|
T | A | 1 | a0001c0001t0002g0215 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.198+17782A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591993 | ||||||
chr16:48592024
|
C | A | 1 | a0001c0001t0002g0216 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.198+17751G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592024 | ||||||
chr16:48592112
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.198+17663A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592112 | ||||||
chr16:48592115
|
C | T | 1 | a0001c0001t0003g0167 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.198+17660G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592115 | ||||||
chr16:48592254
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.198+17521G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592254 | ||||||
chr16:48592255
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.198+17520C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592255 | ||||||
chr16:48592346
|
G | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0101 | 3 | HG02622.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.198+17429C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592346 | ||||||
chr16:48592480
|
C | T | 1 | a0001c0001t0021g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.198+17295G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592480 | ||||||
chr16:48592483
|
C | G | 1 | a0001c0001t0021g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.198+17292G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592483 | ||||||
chr16:48592603
|
A | G | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+17172T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592603 | ||||||
chr16:48592668
|
T | A | 6 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0243others(3): Show | 6 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+17107A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592668 | ||||||
chr16:48593150
|
T | C | 1 | a0001c0001t0002g0179 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.198+16625A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48593150 | ||||||
chr16:48593274
|
C | T | 1 | a0002c0003t0002g0284 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.198+16501G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48593274 | ||||||
chr16:48593395
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.198+16380C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48593395 | ||||||
chr16:48593398
|
A | G | 1 | a0001c0001t0003g0173 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.198+16377T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48593398 | ||||||
chr16:48593813
|
T | C | 2 | a0001c0001t0012g0145a0001c0001t0012g0147 | 2 | NA18993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.198+15962A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48593813 | ||||||
chr16:48593997
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.198+15778C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48593997 | ||||||
chr16:48594001
|
C | CA | 35 | a0001c0001t0001g0004a0001c0001t0001g0057a0001c0001t0001g0074others(32): Show | 38 | HG00621.hp2 HG01175.hp1 HG01516.hp1 others(35): Show |
intron_variant | MODIFIER | c.198+15773dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594001 | ||||||
chr16:48594001
|
C | CAA | 6 | a0001c0001t0001g0077a0001c0002t0004g0008a0001c0002t0004g0031others(3): Show | 7 | HG02055.hp2 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+15772_198+1577 others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594001 | ||||||
chr16:48594001
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0013g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.198+15760_198+1577 others(18): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594001 | ||||||
chr16:48594001
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0014g0037 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.198+15773_198+1577 others(22): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594001 | ||||||
chr16:48594018
|
AC | A | 54 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(51): Show | 60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.198+15756delG | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594018 | ||||||
chr16:48594019
|
C | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(68): Show | 87 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(84): Show |
intron_variant | MODIFIER | c.198+15756G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594019 | ||||||
chr16:48594104
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+15671G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594104 | ||||||
chr16:48594124
|
C | T | 2 | a0001c0001t0016g0143a0001c0001t0017g0142 | 2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.198+15651G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594124 | ||||||
chr16:48594169
|
C | T | 6 | a0001c0001t0001g0053a0001c0001t0001g0089a0001c0001t0001g0091others(3): Show | 6 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+15606G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594169 | ||||||
chr16:48594382
|
T | A | 2 | a0001c0001t0010g0027a0001c0001t0010g0028 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.198+15393A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594382 | ||||||
chr16:48594544
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+15231G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594544 | ||||||
chr16:48594575
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 264 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.198+15200A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594575 | ||||||
chr16:48594608
|
G | A | 1 | a0001c0001t0002g0252 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.198+15167C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594608 | ||||||
chr16:48595170
|
G | A | 1 | a0001c0002t0004g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.198+14605C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595170 | ||||||
chr16:48595277
|
C | G | 1 | a0001c0001t0006g0041 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.198+14498G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595277 | ||||||
chr16:48595289
|
C | T | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+14486G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595289 | ||||||
chr16:48595397
|
T | C | 3 | a0001c0001t0008g0015a0001c0001t0008g0120a0001c0001t0008g0170 | 4 | HG01070.hp1 HG01175.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+14378A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595397 | ||||||
chr16:48595438
|
T | C | 13 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(10): Show | 14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+14337A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595438 | ||||||
chr16:48595456
|
C | CA | 17 | a0001c0001t0002g0021a0001c0001t0002g0179a0001c0001t0002g0183others(14): Show | 19 | HG01106.hp1 HG01256.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+14318dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595456 | ||||||
chr16:48595456
|
C | CAAA | 9 | a0001c0001t0001g0088a0001c0001t0006g0041a0001c0001t0006g0042others(6): Show | 10 | HG01106.hp2 HG01169.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+14316_198+1431 others(7): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595456 | ||||||
chr16:48595456
|
C | CAAAA | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(69): Show | 90 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.198+14315_198+1431 others(8): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595456 | ||||||
chr16:48595456
|
C | CAAAAA | 30 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0045others(27): Show | 33 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.198+14314_198+1431 others(9): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595456 | ||||||
chr16:48595456
|
CA | C | 6 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0106others(3): Show | 6 | HG02818.hp2 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+14318delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595456 | ||||||
chr16:48595456
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+14311_198+1431 others(12): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595456 | ||||||
chr16:48595975
|
A | G | 1 | a0001c0001t0002g0248 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.198+13800T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595975 | ||||||
chr16:48596023
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+13752G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596023 | ||||||
chr16:48596329
|
C | T | 1 | a0001c0001t0003g0144 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.198+13446G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596329 | ||||||
chr16:48596555
|
G | C | 4 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0106others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+13220C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596555 | ||||||
chr16:48596735
|
T | C | 1 | a0001c0001t0003g0171 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.198+13040A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596735 | ||||||
chr16:48596789
|
A | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.198+12986T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596789 | ||||||
chr16:48596861
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.198+12914A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596861 | ||||||
chr16:48596874
|
A | T | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+12901T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596874 | ||||||
chr16:48596883
|
T | C | 4 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0106others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+12892A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596883 | ||||||
chr16:48596980
|
C | T | 2 | a0001c0001t0005g0239a0001c0001t0005g0240 | 2 | HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.198+12795G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596980 | ||||||
chr16:48597118
|
A | G | 2 | a0001c0001t0003g0243a0001c0001t0003g0244 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.198+12657T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597118 | ||||||
chr16:48597242
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.198+12533G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597242 | ||||||
chr16:48597243
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+12532T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597243 | ||||||
chr16:48597268
|
G | A | 2 | a0001c0001t0002g0225a0001c0001t0002g0252 | 2 | NA18974.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.198+12507C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597268 | ||||||
chr16:48597296
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+12479T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597296 | ||||||
chr16:48597434
|
C | G | 3 | a0002c0003t0002g0283a0002c0003t0002g0285a0002c0003t0002g0286 | 3 | NA18939.hp2 NA19011.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.198+12341G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597434 | ||||||
chr16:48597438
|
T | A | 3 | a0002c0003t0002g0283a0002c0003t0002g0285a0002c0003t0002g0286 | 3 | NA18939.hp2 NA19011.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.198+12337A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597438 | ||||||
chr16:48597451
|
C | T | 2 | a0001c0001t0002g0184a0001c0001t0003g0137 | 2 | HG02132.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.198+12324G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597451 | ||||||
chr16:48598567
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+11208G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48598567 | ||||||
chr16:48598613
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.198+11162T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48598613 | ||||||
chr16:48598637
|
A | G | 1 | a0001c0001t0002g0183 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.198+11138T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48598637 | ||||||
chr16:48598847
|
A | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.198+10928T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48598847 | ||||||
chr16:48599194
|
C | T | 3 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0003g0255 | 3 | NA18955.hp2 NA19001.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.198+10581G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48599194 | ||||||
chr16:48599248
|
A | G | 1 | a0001c0001t0003g0144 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.198+10527T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48599248 | ||||||
chr16:48599369
|
T | C | 1 | a0001c0001t0003g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.198+10406A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48599369 | ||||||
chr16:48599814
|
T | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0056a0004c0006t0001g0055 | 3 | HG03239.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.198+9961A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48599814 | ||||||
chr16:48599858
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.198+9917C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48599858 | ||||||
chr16:48599859
|
T | G | 1 | a0001c0001t0010g0027 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.198+9916A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48599859 | ||||||
chr16:48600067
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.198+9708T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600067 | ||||||
chr16:48600156
|
G | C | 3 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182 | 3 | HG01074.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.198+9619C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600156 | ||||||
chr16:48600163
|
A | G | 5 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+9612T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600163 | ||||||
chr16:48600228
|
C | T | 2 | a0001c0001t0016g0143a0001c0001t0017g0142 | 2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.198+9547G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600228 | ||||||
chr16:48600327
|
C | T | 13 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(10): Show | 14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+9448G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600327 | ||||||
chr16:48600534
|
A | G | 1 | a0001c0001t0003g0231 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.198+9241T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600534 | ||||||
chr16:48600600
|
A | T | 1 | a0001c0001t0003g0230 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.198+9175T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600600 | ||||||
chr16:48600848
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.198+8927A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600848 | ||||||
chr16:48600858
|
G | A | 1 | a0001c0001t0002g0122 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.198+8917C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600858 | ||||||
chr16:48601363
|
T | A | 1 | a0001c0001t0023g0083 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.198+8412A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601363 | ||||||
chr16:48601427
|
A | G | 1 | a0001c0001t0003g0141 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.198+8348T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601427 | ||||||
chr16:48601708
|
TG | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.198+8066delC | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601708 | ||||||
chr16:48601710
|
G | T | 107 | a0001c0001t0001g0261a0001c0001t0002g0016a0001c0001t0002g0017others(104): Show | 116 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(113): Show |
intron_variant | MODIFIER | c.198+8065C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601710 | ||||||
chr16:48601781
|
C | T | 1 | a0001c0007t0001g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198+7994G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601781 | ||||||
chr16:48601818
|
T | G | 6 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0005g0239others(3): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+7957A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601818 | ||||||
chr16:48601858
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.198+7917G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601858 | ||||||
chr16:48602057
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.198+7718A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602057 | ||||||
chr16:48602173
|
G | A | 1 | a0001c0001t0008g0120 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.198+7602C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602173 | ||||||
chr16:48602255
|
AAC | A | 5 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+7518_198+7519d others(4): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602255 | ||||||
chr16:48602606
|
T | C | 1 | a0001c0001t0003g0172 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.198+7169A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602606 | ||||||
chr16:48602796
|
A | AAAAT | 5 | a0001c0001t0003g0116a0001c0001t0003g0140a0001c0001t0011g0138others(2): Show | 6 | HG01074.hp1 HG01255.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+6975_198+6978d others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602796 | ||||||
chr16:48602796
|
AAAAT | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 153 | HG00140.hp2 HG00621.hp2 HG00639.hp1 others(150): Show |
intron_variant | MODIFIER | c.198+6975_198+6978d others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602796 | ||||||
chr16:48602796
|
AAAATAAA others(1): Show |
A | 85 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(82): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.198+6971_198+6978d others(10): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602796 | ||||||
chr16:48603003
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.198+6772G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603003 | ||||||
chr16:48603004
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.198+6771C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603004 | ||||||
chr16:48603042
|
T | A | 1 | a0001c0001t0001g0108 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.198+6733A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603042 | ||||||
chr16:48603132
|
T | C | 1 | a0001c0001t0002g0252 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.198+6643A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603132 | ||||||
chr16:48603161
|
C | T | 5 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+6614G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603161 | ||||||
chr16:48603267
|
C | T | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 257 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.198+6508G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603267 | ||||||
chr16:48603276
|
G | A | 1 | a0001c0001t0003g0173 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.198+6499C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603276 | ||||||
chr16:48603462
|
C | T | 2 | a0001c0001t0010g0027a0001c0001t0010g0028 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.198+6313G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603462 | ||||||
chr16:48603560
|
A | C | 3 | a0001c0001t0001g0054a0001c0001t0001g0056a0004c0006t0001g0055 | 3 | HG03239.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.198+6215T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603560 | ||||||
chr16:48603767
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.198+6008G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603767 | ||||||
chr16:48603969
|
C | T | 6 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+5806G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603969 | ||||||
chr16:48604015
|
A | T | 3 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0003g0255 | 3 | NA18955.hp2 NA19001.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.198+5760T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604015 | ||||||
chr16:48604096
|
T | G | 2 | a0001c0001t0002g0175a0001c0001t0003g0174 | 2 | HG00621.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.198+5679A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604096 | ||||||
chr16:48604257
|
T | C | 5 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+5518A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604257 | ||||||
chr16:48604363
|
C | G | 1 | a0003c0005t0003g0013 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198+5412G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604363 | ||||||
chr16:48604436
|
C | T | 2 | a0001c0001t0011g0138a0001c0001t0011g0139 | 2 | HG01074.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.198+5339G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604436 | ||||||
chr16:48604515
|
T | G | 1 | a0003c0005t0003g0013 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198+5260A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604515 | ||||||
chr16:48604548
|
CCAAAGCT others(91): Show |
C | 8 | a0001c0002t0004g0008a0001c0002t0004g0030a0001c0002t0004g0031others(5): Show | 9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+5129_198+5226d others(100): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604548 | ||||||
chr16:48604582
|
C | CA | 5 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+5192dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604582 | ||||||
chr16:48604586
|
A | C | 1 | a0001c0001t0021g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.198+5189T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604586 | ||||||
chr16:48604591
|
A | C | 1 | a0001c0001t0003g0137 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.198+5184T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604591 | ||||||
chr16:48604602
|
T | TA | 14 | a0001c0001t0002g0251a0001c0001t0006g0038a0001c0001t0006g0039others(11): Show | 15 | HG01106.hp2 HG01891.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+5172dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604602 | ||||||
chr16:48604602
|
T | TAA | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.198+5171_198+5172d others(4): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604602 | ||||||
chr16:48604870
|
C | G | 1 | a0001c0001t0002g0176 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.198+4905G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604870 | ||||||
chr16:48605193
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(102): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.198+4582A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605193 | ||||||
chr16:48605251
|
G | A | 103 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(100): Show | 111 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(108): Show |
intron_variant | MODIFIER | c.198+4524C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605251 | ||||||
chr16:48605365
|
G | A | 15 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(12): Show | 16 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.198+4410C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605365 | ||||||
chr16:48605565
|
C | T | 1 | a0001c0002t0004g0008 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.198+4210G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605565 | ||||||
chr16:48605593
|
A | G | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+4182T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605593 | ||||||
chr16:48605812
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(117): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.198+3963A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605812 | ||||||
chr16:48605872
|
T | A | 6 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0003g0232others(3): Show | 6 | HG00280.hp1 HG00738.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+3903A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605872 | ||||||
chr16:48605956
|
A | G | 15 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(12): Show | 16 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.198+3819T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605956 | ||||||
chr16:48606002
|
T | C | 2 | a0001c0001t0003g0236a0001c0001t0003g0237 | 2 | NA18984.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.198+3773A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606002 | ||||||
chr16:48606011
|
T | C | 1 | a0001c0001t0003g0238 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.198+3764A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606011 | ||||||
chr16:48606062
|
C | T | 1 | a0001c0002t0004g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.198+3713G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606062 | ||||||
chr16:48606076
|
C | T | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+3699G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606076 | ||||||
chr16:48606114
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(102): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.198+3661G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606114 | ||||||
chr16:48606175
|
G | A | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+3600C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606175 | ||||||
chr16:48606286
|
C | A | 7 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0109others(4): Show | 7 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+3489G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606286 | ||||||
chr16:48606373
|
C | T | 1 | a0001c0001t0002g0136 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.198+3402G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606373 | ||||||
chr16:48606535
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.198+3240A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606535 | ||||||
chr16:48606721
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(117): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.198+3054A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606721 | ||||||
chr16:48606787
|
T | C | 6 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0005g0239others(3): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+2988A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606787 | ||||||
chr16:48606830
|
A | G | 1 | a0001c0001t0003g0135 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.198+2945T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606830 | ||||||
chr16:48606949
|
T | C | 1 | a0001c0001t0001g0012 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.198+2826A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606949 | ||||||
chr16:48607350
|
A | C | 1 | a0001c0001t0002g0134 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.198+2425T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48607350 | ||||||
chr16:48607563
|
A | G | 1 | a0001c0001t0002g0133 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.198+2212T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48607563 | ||||||
chr16:48607860
|
ATTTGT | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(102): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.198+1910_198+1914d others(7): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48607860 | ||||||
chr16:48607917
|
G | A | 2 | a0001c0001t0003g0243a0001c0001t0003g0244 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.198+1858C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48607917 | ||||||
chr16:48608027
|
A | C | 9 | a0001c0001t0002g0119a0001c0001t0002g0125a0001c0001t0002g0126others(6): Show | 9 | HG01934.hp1 HG02083.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+1748T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608027 | ||||||
chr16:48608170
|
G | GT | 4 | a0001c0001t0001g0273a0001c0001t0001g0275a0001c0001t0002g0247others(1): Show | 4 | NA18963.hp2 NA18988.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1604dupA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608170 | ||||||
chr16:48608180
|
G | T | 13 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(10): Show | 14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+1595C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608180 | ||||||
chr16:48608219
|
A | C | 1 | a0001c0001t0002g0124 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.198+1556T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608219 | ||||||
chr16:48608275
|
T | C | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | NA18962.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.198+1500A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608275 | ||||||
chr16:48608324
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(117): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.198+1451A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608324 | ||||||
chr16:48608568
|
T | A | 1 | a0001c0001t0003g0246 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.198+1207A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608568 | ||||||
chr16:48608659
|
G | T | 1 | a0001c0001t0010g0027 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.198+1116C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608659 | ||||||
chr16:48608682
|
G | C | 3 | a0001c0004t0003g0278a0001c0004t0003g0279a0001c0004t0003g0280 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+1093C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608682 | ||||||
chr16:48608688
|
G | A | 2 | a0001c0001t0013g0036a0001c0001t0014g0037 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+1087C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608688 | ||||||
chr16:48608755
|
T | TA | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 130 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.198+1019dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608755 | ||||||
chr16:48608755
|
TA | T | 6 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0122others(3): Show | 6 | HG01255.hp2 NA18942.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1019delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608755 | ||||||
chr16:48608773
|
C | G | 1 | a0001c0001t0001g0275 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.198+1002G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608773 | ||||||
chr16:48608790
|
G | A | 2 | a0001c0001t0003g0276a0001c0001t0003g0277 | 2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.198+985C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608790 | ||||||
chr16:48608814
|
C | A | 1 | a0001c0001t0002g0252 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.198+961G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608814 | ||||||
chr16:48608981
|
G | A | 5 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(2): Show | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+794C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608981 | ||||||
chr16:48609007
|
G | C | 1 | a0001c0001t0024g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.198+768C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609007 | ||||||
chr16:48609017
|
C | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(102): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.198+758G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609017 | ||||||
chr16:48609048
|
C | CA | 8 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0260others(5): Show | 8 | HG02074.hp2 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+726dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609048 | ||||||
chr16:48609048
|
CA | C | 7 | a0001c0001t0001g0118a0001c0001t0001g0275a0001c0001t0003g0116others(4): Show | 8 | HG02615.hp1 HG02896.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+726delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609048 | ||||||
chr16:48609048
|
CAA | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(113): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.198+725_198+726del others(2): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609048 | ||||||
chr16:48609366
|
A | C | 1 | a0001c0001t0001g0029 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.198+409T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609366 | ||||||
chr16:48609524
|
C | A | 19 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(16): Show | 22 | HG00673.hp1 HG01952.hp2 HG03017.hp2 others(19): Show |
intron_variant | MODIFIER | c.198+251G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609524 | ||||||
chr16:48609699
|
G | A | 2 | a0001c0001t0003g0276a0001c0001t0003g0277 | 2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.198+76C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609699 | ||||||
chr16:48609751
|
C | T | 2 | a0001c0001t0010g0027a0001c0001t0010g0028 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.198+24G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609751 |