geneid | 56954 |
---|---|
ensemblid | ENSG00000114021.12 |
hgncid | 29878 |
symbol | NIT2 |
name | nitrilase family member 2 |
refseq_nuc | NM_020202.5 |
refseq_prot | NP_064587.1 |
ensembl_nuc | ENST00000394140.9 |
ensembl_prot | ENSP00000377696.3 |
mane_status | MANE Select |
chr | chr3 |
start | 100334757 |
end | 100361635 |
strand | + |
ver | v1.2 |
region | chr3:100334757-100361635 |
region5000 | chr3:100329757-100366635 |
regionname0 | NIT2_chr3_100334757_100361635 |
regionname5000 | NIT2_chr3_100329757_100366635 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 276 | 394 | 80 | 72 | 184 | 12 | 46 | 144 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0002 | 0/0 | 276 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0003 | 0/0 | 276 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 831 | 391 | 77 | 72 | 184 | 12 | 46 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
c0002 | 0/0 | 831 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
c0003 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
c0004 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 6401 | 91 | 17 | 6 | 65 | 0 | 3 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0002 | 0/0 | 6402 | 63 | 1 | 15 | 32 | 4 | 11 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0003 | 0/0 | 6403 | 59 | 5 | 18 | 19 | 4 | 13 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0004 | 0/0 | 6402 | 37 | 1 | 2 | 32 | 0 | 2 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0005 | 0/0 | 6402 | 31 | 1 | 15 | 8 | 0 | 7 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0006 | 0/0 | 6402 | 15 | 13 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0007 | 0/0 | 6395 | 5 | 5 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0008 | 0/0 | 6401 | 5 | 5 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0009 | 0/0 | 6402 | 5 | 0 | 1 | 3 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0010 | 0/0 | 6403 | 5 | 0 | 0 | 5 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0011 | 0/0 | 6402 | 4 | 3 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0012 | 0/0 | 6399 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0013 | 0/0 | 6402 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0014 | 0/0 | 6402 | 3 | 0 | 2 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0015 | 0/0 | 6401 | 3 | 0 | 3 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0016 | 0/0 | 6401 | 3 | 2 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0017 | 0/0 | 6401 | 3 | 1 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0018 | 0/0 | 6402 | 3 | 0 | 0 | 3 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0019 | 0/0 | 6402 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0020 | 0/0 | 6403 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0021 | 0/0 | 6401 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0022 | 0/0 | 6400 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0023 | 0/0 | 6401 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0024 | 0/0 | 6401 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0025 | 0/0 | 6403 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0026 | 0/0 | 6403 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0027 | 0/0 | 6403 | 2 | 0 | 0 | 1 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0028 | 0/0 | 6402 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0029 | 0/0 | 6402 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0030 | 0/0 | 6379 | 2 | 0 | 0 | 0 | 0 | 2 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0031 | 0/0 | 6402 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0032 | 0/0 | 6402 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0033 | 0/0 | 6401 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0034 | 0/0 | 6401 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0035 | 0/0 | 6395 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0036 | 0/0 | 6400 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0037 | 0/0 | 6402 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0038 | 0/0 | 6402 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0039 | 0/0 | 6401 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0040 | 0/0 | 6401 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0041 | 0/0 | 6401 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0042 | 0/0 | 6401 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0043 | 0/0 | 6402 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0044 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0045 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0046 | 0/0 | 6401 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0047 | 0/0 | 6402 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0048 | 0/0 | 6401 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0049 | 0/0 | 6402 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0050 | 0/0 | 6403 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0051 | 0/0 | 6402 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0052 | 0/0 | 6401 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0053 | 0/0 | 6403 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0054 | 0/0 | 6403 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0055 | 0/0 | 6402 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0056 | 0/0 | 6402 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0057 | 0/0 | 6402 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0058 | 0/0 | 6403 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0059 | 0/0 | 6403 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0060 | 0/0 | 6403 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
t0061 | 0/0 | 6404 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 39 | 0 | 5 | 26 | 1 | 7 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0002 | 0/0 | 36 | 5 | 3 | 26 | 0 | 2 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0003 | 0/0 | 25 | 0 | 4 | 15 | 2 | 4 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0004 | 0/0 | 24 | 0 | 0 | 24 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0005 | 0/0 | 21 | 5 | 8 | 0 | 2 | 6 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0006 | 0/0 | 17 | 4 | 9 | 0 | 1 | 3 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0007 | 0/0 | 16 | 3 | 5 | 7 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0008 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0009 | 0/0 | 7 | 2 | 2 | 3 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0010 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0014 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0015 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 831 | 391 | 77 | 72 | 184 | 12 | 46 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0002 | 0/0 | 831 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0002c0004 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0003c0003 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7231 | 91 | 17 | 6 | 65 | 0 | 3 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0002 | 0/0 | 7232 | 63 | 1 | 15 | 32 | 4 | 11 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0003 | 0/0 | 7233 | 59 | 5 | 18 | 19 | 4 | 13 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0004 | 0/0 | 7232 | 37 | 1 | 2 | 32 | 0 | 2 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0005 | 0/0 | 7232 | 30 | 1 | 15 | 7 | 0 | 7 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0006 | 0/0 | 7232 | 15 | 13 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0007 | 0/0 | 7225 | 5 | 5 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0008 | 0/0 | 7231 | 5 | 5 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0009 | 0/0 | 7232 | 5 | 0 | 1 | 3 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0010 | 0/0 | 7233 | 4 | 0 | 0 | 4 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0011 | 0/0 | 7232 | 4 | 3 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0012 | 0/0 | 7229 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0013 | 0/0 | 7232 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0014 | 0/0 | 7232 | 3 | 0 | 2 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0015 | 0/0 | 7231 | 3 | 0 | 3 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0016 | 0/0 | 7231 | 3 | 2 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0017 | 0/0 | 7231 | 3 | 1 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0018 | 0/0 | 7232 | 3 | 0 | 0 | 3 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0020 | 0/0 | 7233 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0021 | 0/0 | 7231 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0022 | 0/0 | 7230 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0023 | 0/0 | 7231 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0024 | 0/0 | 7231 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0025 | 0/0 | 7233 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0026 | 0/0 | 7233 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0027 | 0/0 | 7233 | 2 | 0 | 0 | 1 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0028 | 0/0 | 7232 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0029 | 0/0 | 7232 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0030 | 0/0 | 7209 | 2 | 0 | 0 | 0 | 0 | 2 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0032 | 0/0 | 7232 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0033 | 0/0 | 7231 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0034 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0035 | 0/0 | 7225 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0036 | 0/0 | 7230 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0037 | 0/0 | 7232 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0038 | 0/0 | 7232 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0039 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0040 | 0/0 | 7231 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0041 | 0/0 | 7231 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0042 | 0/0 | 7231 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0043 | 0/0 | 7232 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0044 | 0/0 | 7233 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0045 | 0/0 | 7233 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0046 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0047 | 0/0 | 7232 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0048 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0049 | 0/0 | 7232 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0050 | 0/0 | 7233 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0051 | 0/0 | 7232 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0052 | 0/0 | 7231 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0053 | 0/0 | 7233 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0054 | 0/0 | 7233 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0055 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0056 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0057 | 0/0 | 7232 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0058 | 0/0 | 7233 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0059 | 0/0 | 7233 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0060 | 0/0 | 7233 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0001t0061 | 0/0 | 7234 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0002t0019 | 0/0 | 7232 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0001c0002t0031 | 0/0 | 7232 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0002c0004t0005 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
a0003c0003t0010 | 0/0 | 7233 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | copy fasta | chr3 | 100329757 | 100366635 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 22 | 0 | 0 | 22 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0007 | 0/0 | 11 | 3 | 2 | 6 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0008 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0009 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0001 | 0/0 | 34 | 0 | 4 | 23 | 1 | 6 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0010 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0003 | 0/0 | 22 | 0 | 3 | 14 | 2 | 3 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0005 | 0/0 | 18 | 5 | 8 | 0 | 0 | 5 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0014 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0004g0002 | 0/0 | 27 | 1 | 2 | 22 | 0 | 2 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0004g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0005g0006 | 0/0 | 12 | 0 | 9 | 0 | 0 | 3 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0005g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0005g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0005g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0006g0002 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0006g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0006g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0007g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0008g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0009g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0009g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0009g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0010g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0010g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0011g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0011g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0013g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0014g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0015g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0016g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0017g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0017g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0018g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0020g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0020g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0021g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0022g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0023g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0024g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0025g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0026g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0027g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0027g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0028g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0029g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0030g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0030g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0032g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0033g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0034g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0035g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0036g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0037g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0038g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0039g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0040g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0041g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0042g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0043g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0044g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0045g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0046g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0047g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0048g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0049g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0050g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0051g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0052g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0053g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0054g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0055g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0056g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0057g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0058g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0059g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0060g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0001t0061g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0002t0019g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0001c0002t0031g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0002c0004t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
a0003c0003t0010g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0003 | g0062 | EUR | GBR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00280 | hp1 | a0001 | c0001 | t0058 | g0028 | EUR | FIN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00280 | hp2 | a0001 | c0001 | t0059 | g0005 | EUR | FIN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00323 | hp2 | a0001 | c0001 | t0037 | g0006 | EUR | FIN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00544 | hp2 | a0001 | c0001 | t0029 | g0041 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00639 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00642 | hp2 | a0001 | c0001 | t0014 | g0015 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00735 | hp2 | a0001 | c0001 | t0016 | g0020 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0027 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0108 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0095 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01243 | hp2 | a0001 | c0001 | t0011 | g0024 | AMR | PUR | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01346 | hp2 | a0001 | c0001 | t0014 | g0015 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01358 | hp2 | a0001 | c0001 | t0042 | g0026 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01496 | hp1 | a0001 | c0001 | t0015 | g0007 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01516 | hp1 | a0001 | c0001 | t0050 | g0005 | EUR | IBS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0086 | EUR | IBS | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0098 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01952 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01978 | hp1 | a0001 | c0001 | t0015 | g0007 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01981 | hp2 | a0001 | c0001 | t0032 | g0066 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01993 | hp1 | a0001 | c0001 | t0026 | g0037 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02015 | hp1 | a0001 | c0001 | t0023 | g0009 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02015 | hp2 | a0001 | c0001 | t0021 | g0002 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0099 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02055 | hp2 | a0001 | c0001 | t0011 | g0024 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02071 | hp2 | a0001 | c0001 | t0023 | g0009 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02074 | hp2 | a0001 | c0001 | t0055 | g0001 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02132 | hp1 | a0001 | c0001 | t0036 | g0013 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02135 | hp2 | a0001 | c0001 | t0005 | g0091 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02145 | hp2 | a0001 | c0001 | t0045 | g0006 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | CDX | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CDX | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | CDX | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CDX | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02257 | hp1 | a0001 | c0001 | t0025 | g0035 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02280 | hp1 | a0001 | c0001 | t0022 | g0034 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02293 | hp1 | a0001 | c0001 | t0052 | g0003 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02300 | hp2 | a0001 | c0001 | t0015 | g0007 | AMR | PEL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02572 | hp1 | a0001 | c0001 | t0020 | g0135 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02572 | hp2 | a0001 | c0001 | t0047 | g0107 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02602 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02602 | hp2 | a0001 | c0001 | t0043 | g0015 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02615 | hp1 | a0001 | c0001 | t0048 | g0130 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02615 | hp2 | a0001 | c0001 | t0013 | g0006 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02622 | hp2 | a0001 | c0001 | t0016 | g0020 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02630 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02683 | hp2 | a0001 | c0001 | t0030 | g0001 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02717 | hp2 | a0001 | c0001 | t0013 | g0006 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0024 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0093 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02809 | hp2 | a0001 | c0002 | t0019 | g0023 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02896 | hp2 | a0001 | c0001 | t0012 | g0131 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02965 | hp2 | a0001 | c0001 | t0013 | g0006 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02970 | hp1 | a0001 | c0001 | t0044 | g0102 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02970 | hp2 | a0001 | c0001 | t0025 | g0035 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03017 | hp1 | a0001 | c0001 | t0054 | g0005 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03041 | hp2 | a0001 | c0002 | t0031 | g0023 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03098 | hp1 | a0001 | c0001 | t0011 | g0073 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03098 | hp2 | a0001 | c0001 | t0049 | g0020 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03130 | hp1 | a0001 | c0001 | t0035 | g0069 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0067 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03139 | hp2 | a0001 | c0001 | t0012 | g0132 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0070 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03209 | hp1 | a0001 | c0001 | t0046 | g0068 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03209 | hp2 | a0001 | c0001 | t0038 | g0071 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03225 | hp1 | a0001 | c0001 | t0022 | g0034 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03486 | hp1 | a0001 | c0001 | t0039 | g0011 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03486 | hp2 | a0001 | c0001 | t0020 | g0074 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03490 | hp1 | a0001 | c0001 | t0051 | g0055 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0134 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03579 | hp1 | a0001 | c0001 | t0061 | g0049 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03669 | hp2 | a0001 | c0001 | t0014 | g0015 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03831 | hp2 | a0001 | c0001 | t0053 | g0003 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0027 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03834 | hp2 | a0001 | c0001 | t0033 | g0126 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG04115 | hp2 | a0001 | c0001 | t0009 | g0007 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG04184 | hp2 | a0001 | c0001 | t0005 | g0094 | SAS | BEB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG04199 | hp1 | a0001 | c0001 | t0005 | g0096 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG04199 | hp2 | a0001 | c0001 | t0027 | g0010 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG04204 | hp2 | a0001 | c0001 | t0030 | g0082 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0124 | SAS | STU | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18522 | hp1 | a0001 | c0001 | t0016 | g0020 | AFR | YRI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | YRI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18612 | hp2 | a0001 | c0001 | t0024 | g0048 | EAS | CHB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | YRI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18940 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18940 | hp2 | a0002 | c0004 | t0005 | g0092 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18946 | hp1 | a0001 | c0001 | t0017 | g0081 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18948 | hp2 | a0001 | c0001 | t0040 | g0121 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18953 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18956 | hp1 | a0001 | c0001 | t0028 | g0038 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18961 | hp2 | a0001 | c0001 | t0060 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18963 | hp2 | a0001 | c0001 | t0024 | g0048 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18965 | hp1 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18970 | hp2 | a0001 | c0001 | t0041 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18971 | hp1 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18972 | hp1 | a0001 | c0001 | t0010 | g0103 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18974 | hp2 | a0001 | c0001 | t0005 | g0097 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18981 | hp1 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18988 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18991 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19002 | hp1 | a0001 | c0001 | t0056 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19009 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19010 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0065 | AFR | LWK | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19043 | hp1 | a0001 | c0001 | t0017 | g0064 | AFR | LWK | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | LWK | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19054 | hp1 | a0001 | c0001 | t0021 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19060 | hp2 | a0003 | c0003 | t0010 | g0021 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19064 | hp1 | a0001 | c0001 | t0018 | g0016 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19066 | hp1 | a0001 | c0001 | t0027 | g0088 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19066 | hp2 | a0001 | c0001 | t0029 | g0041 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19067 | hp2 | a0001 | c0001 | t0028 | g0038 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19070 | hp2 | a0001 | c0001 | t0018 | g0016 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19084 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19087 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19089 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19090 | hp1 | a0001 | c0001 | t0010 | g0105 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0104 | AFR | YRI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ASW | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0054 | EUR | TSI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0080 | EUR | TSI | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | GIH | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01123 | hp1 | a0001 | c0001 | t0057 | g0001 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG01123 | hp2 | a0001 | c0001 | t0026 | g0037 | AMR | CLM | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02109 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02559 | hp1 | a0001 | c0001 | t0034 | g0129 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | ACB | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG03471 | hp2 | a0001 | c0002 | t0019 | g0023 | AFR | MSL | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG06807 | hp1 | a0001 | c0001 | t0012 | g0133 | AFR | USA | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | USA | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
NA18955 | hp2 | a0001 | c0001 | t0018 | g0016 | EAS | JPT | NIT2_chr3_100329757_100366635 | NIT2 | chr3 | 100329757 | 100366635 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100334767
|
GCAGGTGG others(16): Show |
G | 1 | a0001 | 2 | HG02683.hp2 HG04204.hp2 |
frameshift_variant&start_lost | HIGH | c.-22_1delGGTGGTGCTT others(13): Show |
p.Met1fs | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/10 | 14/7233 | 1/831 | 1/276 | INFO_REALIGN_3_PRIME | chr3 | 100334767 | |
chr3:100345601
|
T | C | 1 | a0003 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.353T>C | p.Ile118Thr | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 5/10 | 388/7233 | 353/831 | 118/276 | chr3 | 100345601 | ||
chr3:100355226
|
G | C | 1 | a0002 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.789G>C | p.Gln263His | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 824/7233 | 789/831 | 263/276 | chr3 | 100355226 | ||
chr3:100355227
|
A | T | 1 | a0002 | 1 | NA18940.hp2 | stop_gained | HIGH | c.790A>T | p.Lys264* | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 825/7233 | 790/831 | 264/276 | chr3 | 100355227 | ||
chr3:100355229
|
G | T | 1 | a0002 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.792G>T | p.Lys264Asn | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 827/7233 | 792/831 | 264/276 | chr3 | 100355229 | ||
chr3:100355231
|
G | C | 1 | a0002 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.794G>C | p.Arg265Pro | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 829/7233 | 794/831 | 265/276 | chr3 | 100355231 | ||
chr3:100355237
|
A | T | 1 | a0002 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.800A>T | p.Asp267Val | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 835/7233 | 800/831 | 267/276 | chr3 | 100355237 | ||
chr3:100355238
|
C | G | 1 | a0002 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.801C>G | p.Asp267Glu | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 836/7233 | 801/831 | 267/276 | chr3 | 100355238 | ||
chr3:100355239
|
C | A | 1 | a0002 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.802C>A | p.Leu268Ile | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 837/7233 | 802/831 | 268/276 | chr3 | 100355239 | ||
chr3:100361634
|
A | G | 1 | a0001 | 1 | NA18948.hp2 | splice_region_variant | LOW | c.*6366A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | chr3 | 100361634 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100352488
|
C | T | 1 | a0001c0002 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.669C>T | p.Thr223Thr | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/10 | 704/7233 | 669/831 | 223/276 | chr3 | 100352488 | ||
chr3:100355230
|
C | A | 1 | a0002c0004 | 1 | NA18940.hp2 | synonymous_variant | LOW | c.793C>A | p.Arg265Arg | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 828/7233 | 793/831 | 265/276 | chr3 | 100355230 | ||
chr3:100355241
|
C | T | 1 | a0002c0004 | 1 | NA18940.hp2 | synonymous_variant | LOW | c.804C>T | p.Leu268Leu | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 839/7233 | 804/831 | 268/276 | chr3 | 100355241 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100334757
|
A | G | 1 | a0001c0001t0061 | 1 | HG03579.hp1 | 5_prime_UTR_variant | MODIFIER | c.-35A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/10 | 35 | chr3 | 100334757 | |||||
chr3:100355302
|
G | A | 2 | a0001c0002t0019a0001c0002t0031 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*34G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 34 | chr3 | 100355302 | |||||
chr3:100355410
|
A | G | 1 | a0001c0001t0029 | 2 | HG00544.hp2 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*142A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 142 | chr3 | 100355410 | |||||
chr3:100355558
|
G | A | 1 | a0001c0001t0020 | 2 | HG02572.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*290G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 290 | chr3 | 100355558 | |||||
chr3:100355852
|
C | T | 1 | a0001c0002t0031 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*584C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 584 | chr3 | 100355852 | |||||
chr3:100355891
|
T | C | 1 | a0001c0001t0032 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*623T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 623 | chr3 | 100355891 | |||||
chr3:100355915
|
G | C | 41 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(38): Show | 243 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*647G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 647 | chr3 | 100355915 | |||||
chr3:100355928
|
T | C | 1 | a0001c0001t0033 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*660T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 660 | chr3 | 100355928 | |||||
chr3:100355940
|
G | T | 2 | a0001c0001t0016a0001c0001t0049 | 4 | HG00735.hp2 HG02622.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*672G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 672 | chr3 | 100355940 | |||||
chr3:100356006
|
C | T | 1 | a0001c0001t0011 | 4 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*738C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 738 | chr3 | 100356006 | |||||
chr3:100356065
|
C | T | 2 | a0001c0001t0060a0001c0002t0031 | 2 | HG03041.hp2 NA18961.hp2 |
3_prime_UTR_variant | MODIFIER | c.*797C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 797 | chr3 | 100356065 | |||||
chr3:100356247
|
G | T | 1 | a0001c0001t0015 | 3 | HG01496.hp1 HG01978.hp1 HG02300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*979G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 979 | chr3 | 100356247 | |||||
chr3:100356331
|
A | G | 1 | a0001c0001t0025 | 2 | HG02257.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1063A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1063 | chr3 | 100356331 | |||||
chr3:100356544
|
G | A | 2 | a0001c0001t0012a0001c0001t0034 | 4 | HG02559.hp1 HG02896.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1276G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1276 | chr3 | 100356544 | |||||
chr3:100356675
|
A | T | 1 | a0001c0001t0028 | 2 | NA18956.hp1 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1407A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1407 | chr3 | 100356675 | |||||
chr3:100356811
|
A | C | 3 | a0001c0001t0020a0001c0002t0019a0001c0002t0031 | 5 | HG02572.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1543A>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1543 | chr3 | 100356811 | |||||
chr3:100356820
|
A | G | 1 | a0001c0001t0059 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1552A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1552 | chr3 | 100356820 | |||||
chr3:100356915
|
G | T | 2 | a0001c0001t0034a0001c0001t0048 | 2 | HG02559.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1647G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1647 | chr3 | 100356915 | |||||
chr3:100357119
|
A | T | 1 | a0001c0001t0058 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1851A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 1851 | chr3 | 100357119 | |||||
chr3:100357379
|
T | A | 1 | a0001c0001t0050 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2111T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2111 | chr3 | 100357379 | |||||
chr3:100357637
|
C | CT | 12 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(9): Show | 25 | HG01069.hp1 HG02109.hp2 HG02145.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2391dupT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2392 | INFO_REALIGN_3_PRIME | chr3 | 100357637 | ||||
chr3:100357637
|
CT | C | 7 | a0001c0001t0012a0001c0001t0017a0001c0001t0021others(4): Show | 12 | HG02015.hp2 HG02132.hp1 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2391delT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2391 | INFO_REALIGN_3_PRIME | chr3 | 100357637 | ||||
chr3:100357637
|
CTTTTTTT | C | 2 | a0001c0001t0007a0001c0001t0035 | 6 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2385_*2391delTTTT others(3): Show |
NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2385 | INFO_REALIGN_3_PRIME | chr3 | 100357637 | ||||
chr3:100357672
|
C | T | 20 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(17): Show | 164 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*2404C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2404 | chr3 | 100357672 | |||||
chr3:100357723
|
T | G | 1 | a0001c0001t0037 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2455T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2455 | chr3 | 100357723 | |||||
chr3:100357726
|
A | G | 3 | a0001c0001t0008a0001c0001t0022a0001c0001t0046 | 8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2458A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2458 | chr3 | 100357726 | |||||
chr3:100357844
|
C | G | 53 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(50): Show | 327 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(324): Show |
3_prime_UTR_variant | MODIFIER | c.*2576C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2576 | chr3 | 100357844 | |||||
chr3:100357979
|
T | C | 15 | a0001c0001t0001a0001c0001t0009a0001c0001t0012others(12): Show | 118 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2711T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2711 | chr3 | 100357979 | |||||
chr3:100357997
|
C | T | 1 | a0001c0001t0042 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2729C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2729 | chr3 | 100357997 | |||||
chr3:100357998
|
G | A | 1 | a0001c0001t0046 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2730G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2730 | chr3 | 100357998 | |||||
chr3:100358019
|
C | A | 8 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(5): Show | 64 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2751C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2751 | chr3 | 100358019 | |||||
chr3:100358034
|
TC | T | 51 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(48): Show | 324 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*2770delC | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2770 | INFO_REALIGN_3_PRIME | chr3 | 100358034 | ||||
chr3:100358067
|
C | T | 1 | a0001c0001t0061 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2799C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2799 | chr3 | 100358067 | |||||
chr3:100358136
|
A | G | 11 | a0001c0001t0002a0001c0001t0011a0001c0001t0017others(8): Show | 83 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2868A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 2868 | chr3 | 100358136 | |||||
chr3:100358377
|
C | T | 1 | a0001c0001t0057 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3109C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3109 | chr3 | 100358377 | |||||
chr3:100358633
|
A | G | 1 | a0001c0001t0024 | 2 | NA18612.hp2 NA18963.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3365A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3365 | chr3 | 100358633 | |||||
chr3:100358795
|
C | T | 1 | a0001c0001t0041 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3527C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3527 | chr3 | 100358795 | |||||
chr3:100358800
|
G | A | 1 | a0001c0001t0025 | 2 | HG02257.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3532G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3532 | chr3 | 100358800 | |||||
chr3:100358894
|
C | T | 1 | a0001c0001t0054 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3626C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3626 | chr3 | 100358894 | |||||
chr3:100359217
|
T | G | 1 | a0001c0001t0011 | 4 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3949T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3949 | chr3 | 100359217 | |||||
chr3:100359239
|
C | T | 1 | a0001c0001t0047 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3971C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 3971 | chr3 | 100359239 | |||||
chr3:100359541
|
C | A | 1 | a0001c0001t0026 | 2 | HG01123.hp2 HG01993.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4273C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 4273 | chr3 | 100359541 | |||||
chr3:100359542
|
C | T | 1 | a0001c0001t0023 | 2 | HG02015.hp1 HG02071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4274C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 4274 | chr3 | 100359542 | |||||
chr3:100359566
|
CCT | C | 5 | a0001c0001t0008a0001c0001t0012a0001c0001t0022others(2): Show | 12 | HG02109.hp2 HG02280.hp1 HG02293.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4304_*4305delTC | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 4304 | INFO_REALIGN_3_PRIME | chr3 | 100359566 | ||||
chr3:100359777
|
C | T | 1 | a0001c0001t0013 | 3 | HG02615.hp2 HG02717.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4509C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 4509 | chr3 | 100359777 | |||||
chr3:100359850
|
G | C | 3 | a0001c0001t0008a0001c0001t0022a0001c0001t0046 | 8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4582G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 4582 | chr3 | 100359850 | |||||
chr3:100360460
|
C | T | 1 | a0001c0001t0053 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5192C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5192 | chr3 | 100360460 | |||||
chr3:100360544
|
T | C | 1 | a0001c0001t0018 | 3 | NA18955.hp2 NA19064.hp1 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5276T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5276 | chr3 | 100360544 | |||||
chr3:100360575
|
C | A | 3 | a0001c0001t0008a0001c0001t0022a0001c0001t0046 | 8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5307C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5307 | chr3 | 100360575 | |||||
chr3:100360603
|
G | T | 14 | a0001c0001t0001a0001c0001t0009a0001c0001t0015others(11): Show | 114 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*5335G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5335 | chr3 | 100360603 | |||||
chr3:100360638
|
C | T | 1 | a0001c0001t0056 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5370C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5370 | chr3 | 100360638 | |||||
chr3:100360795
|
C | T | 3 | a0001c0001t0008a0001c0001t0022a0001c0001t0046 | 8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5527C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5527 | chr3 | 100360795 | |||||
chr3:100360892
|
G | A | 1 | a0001c0001t0013 | 3 | HG02615.hp2 HG02717.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5624G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 5624 | chr3 | 100360892 | |||||
chr3:100361289
|
T | A | 1 | a0001c0001t0043 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6021T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 6021 | chr3 | 100361289 | |||||
chr3:100361302
|
AT | A | 14 | a0001c0001t0001a0001c0001t0009a0001c0001t0015others(11): Show | 114 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*6035delT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 6035 | chr3 | 100361302 | |||||
chr3:100361354
|
T | G | 7 | a0001c0001t0005a0001c0001t0013a0001c0001t0029others(4): Show | 39 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*6086T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 6086 | chr3 | 100361354 | |||||
chr3:100361495
|
G | A | 1 | a0001c0001t0055 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6227G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 6227 | chr3 | 100361495 | |||||
chr3:100361602
|
T | C | 2 | a0001c0001t0014a0001c0001t0043 | 4 | HG00642.hp2 HG01346.hp2 HG02602.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6334T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 10/10 | 6334 | chr3 | 100361602 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100334807
|
C | T | 1 | a0001c0001t0020g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.7+9C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100334807 | ||||||
chr3:100334808
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0061g0049 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.7+10G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100334808 | ||||||
chr3:100334840
|
C | CG | 139 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(136): Show | 320 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(317): Show |
intron_variant | MODIFIER | c.7+47dupG | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100334840 | |||||
chr3:100334892
|
C | A | 1 | a0001c0001t0001g0063 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.7+94C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100334892 | ||||||
chr3:100334960
|
C | G | 1 | a0001c0001t0008g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.7+162C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100334960 | ||||||
chr3:100335044
|
C | T | 5 | a0001c0001t0012g0131a0001c0001t0012g0132a0001c0001t0012g0133others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+246C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335044 | ||||||
chr3:100335157
|
T | A | 1 | a0001c0001t0017g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7+359T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335157 | ||||||
chr3:100335276
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7+478A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335276 | ||||||
chr3:100335316
|
A | G | 47 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.7+518A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335316 | ||||||
chr3:100335342
|
G | A | 1 | a0001c0001t0009g0108 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.7+544G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335342 | ||||||
chr3:100335408
|
A | C | 1 | a0001c0001t0047g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.7+610A>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335408 | ||||||
chr3:100335472
|
T | C | 1 | a0001c0001t0005g0065 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.7+674T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335472 | ||||||
chr3:100335646
|
G | T | 34 | a0001c0001t0001g0040a0001c0001t0004g0002a0001c0001t0004g0042others(31): Show | 94 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.7+848G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335646 | ||||||
chr3:100335779
|
G | A | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0032g0066 | 5 | HG00741.hp2 HG01361.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+981G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335779 | ||||||
chr3:100335784
|
G | T | 2 | a0001c0001t0001g0127a0001c0001t0033g0126 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.7+986G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335784 | ||||||
chr3:100335802
|
A | T | 46 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 110 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.7+1004A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335802 | ||||||
chr3:100335890
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7+1092A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100335890 | ||||||
chr3:100336004
|
G | T | 1 | a0001c0001t0002g0039 | 2 | HG01258.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.7+1206G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336004 | ||||||
chr3:100336007
|
C | A | 2 | a0001c0001t0034g0129a0001c0001t0048g0130 | 2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.7+1209C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336007 | ||||||
chr3:100336169
|
C | T | 2 | a0001c0001t0002g0089a0001c0001t0002g0090 | 2 | HG02155.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.7+1371C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336169 | ||||||
chr3:100336197
|
C | T | 5 | a0001c0001t0012g0131a0001c0001t0012g0132a0001c0001t0012g0133others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+1399C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336197 | ||||||
chr3:100336281
|
C | T | 33 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0016others(30): Show | 78 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.7+1483C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336281 | ||||||
chr3:100336302
|
A | G | 46 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 110 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.7+1504A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336302 | ||||||
chr3:100336429
|
G | A | 130 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(127): Show | 307 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(304): Show |
intron_variant | MODIFIER | c.7+1631G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336429 | ||||||
chr3:100336471
|
T | C | 46 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 110 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.7+1673T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336471 | ||||||
chr3:100336493
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.7+1695A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336493 | ||||||
chr3:100336497
|
A | AT | 5 | a0001c0001t0012g0131a0001c0001t0012g0132a0001c0001t0012g0133others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+1700dupT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100336497 | |||||
chr3:100336506
|
C | T | 5 | a0001c0001t0012g0131a0001c0001t0012g0132a0001c0001t0012g0133others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+1708C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336506 | ||||||
chr3:100336520
|
G | A | 5 | a0001c0001t0012g0131a0001c0001t0012g0132a0001c0001t0012g0133others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+1722G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336520 | ||||||
chr3:100336610
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | NA18975.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.7+1812G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336610 | ||||||
chr3:100336760
|
C | T | 6 | a0001c0001t0011g0024a0001c0001t0011g0073a0001c0001t0017g0064others(3): Show | 9 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+1962C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336760 | ||||||
chr3:100336770
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0061g0049 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.7+1972C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336770 | ||||||
chr3:100336833
|
G | A | 1 | a0001c0001t0011g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7+2035G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336833 | ||||||
chr3:100336835
|
T | G | 1 | a0001c0001t0011g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7+2037T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336835 | ||||||
chr3:100336876
|
C | T | 1 | a0001c0001t0003g0124 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.7+2078C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100336876 | ||||||
chr3:100337030
|
T | G | 1 | a0001c0001t0002g0075 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.8-2057T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337030 | ||||||
chr3:100337160
|
A | G | 47 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.8-1927A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337160 | ||||||
chr3:100337162
|
T | G | 1 | a0001c0001t0020g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.8-1925T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337162 | ||||||
chr3:100337173
|
T | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.8-1914T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337173 | ||||||
chr3:100337234
|
G | A | 1 | a0001c0001t0001g0019 | 4 | HG02109.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-1853G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337234 | ||||||
chr3:100337334
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.8-1753G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337334 | ||||||
chr3:100337482
|
C | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.8-1605C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337482 | ||||||
chr3:100337510
|
G | T | 2 | a0001c0001t0017g0064a0001c0001t0020g0074 | 2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.8-1577G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337510 | ||||||
chr3:100337541
|
A | T | 1 | a0001c0001t0027g0088 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.8-1546A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337541 | ||||||
chr3:100337655
|
C | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.8-1432C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337655 | ||||||
chr3:100337656
|
G | A | 1 | a0001c0001t0034g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.8-1431G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337656 | ||||||
chr3:100337748
|
C | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0024g0048 | 4 | NA18612.hp2 NA18963.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-1339C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337748 | ||||||
chr3:100337765
|
T | C | 2 | a0001c0002t0019g0023a0001c0002t0031g0023 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.8-1322T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337765 | ||||||
chr3:100337771
|
A | T | 1 | a0001c0001t0002g0087 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.8-1316A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337771 | ||||||
chr3:100337772
|
T | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0077a0001c0001t0027g0010 | 7 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1315T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337772 | ||||||
chr3:100337943
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.8-1144T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100337943 | ||||||
chr3:100338001
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.8-1086G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338001 | ||||||
chr3:100338049
|
C | T | 5 | a0001c0001t0007g0011a0001c0001t0007g0070a0001c0001t0035g0069others(2): Show | 8 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-1038C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338049 | ||||||
chr3:100338050
|
G | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.8-1037G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338050 | ||||||
chr3:100338163
|
T | C | 1 | a0001c0001t0012g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.8-924T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338163 | ||||||
chr3:100338265
|
A | G | 21 | a0001c0001t0004g0002a0001c0001t0004g0021a0001c0001t0004g0031others(18): Show | 64 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.8-822A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338265 | ||||||
chr3:100338359
|
A | G | 142 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(139): Show | 324 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(321): Show |
intron_variant | MODIFIER | c.8-728A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338359 | ||||||
chr3:100338425
|
C | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.8-662C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338425 | ||||||
chr3:100338573
|
T | G | 53 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 120 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.8-514T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338573 | ||||||
chr3:100338826
|
C | T | 1 | a0001c0001t0002g0033 | 2 | HG00741.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.8-261C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338826 | ||||||
chr3:100338859
|
G | A | 1 | a0001c0001t0061g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.8-228G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338859 | ||||||
chr3:100338940
|
C | G | 1 | a0001c0001t0034g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.8-147C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338940 | ||||||
chr3:100338991
|
CG | C | 3 | a0001c0001t0001g0040a0001c0001t0020g0135a0001c0001t0047g0107 | 4 | HG02572.hp1 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-92delG | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100338991 | |||||
chr3:100338999
|
TAA | T | 3 | a0001c0001t0001g0040a0001c0001t0020g0135a0001c0001t0047g0107 | 4 | HG02572.hp1 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-87_8-86delAA | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100338999 | ||||||
chr3:100339002
|
C | A | 2 | a0001c0001t0004g0021a0003c0003t0010g0021 | 3 | NA18988.hp2 NA19060.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.8-85C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100339002 | ||||||
chr3:100339002
|
C | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 120 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.8-85C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100339002 | ||||||
chr3:100339048
|
G | A | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | NA18950.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.8-39G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 1/9 | chr3 | 100339048 | ||||||
chr3:100339258
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 120 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.126+53G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339258 | ||||||
chr3:100339294
|
G | A | 1 | a0001c0001t0003g0051 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.126+89G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339294 | ||||||
chr3:100339361
|
G | A | 28 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(25): Show | 54 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.126+156G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339361 | ||||||
chr3:100339456
|
T | C | 24 | a0001c0001t0001g0040a0001c0001t0005g0006a0001c0001t0005g0012others(21): Show | 48 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.126+251T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339456 | ||||||
chr3:100339472
|
A | C | 1 | a0001c0001t0029g0041 | 2 | HG00544.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.126+267A>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339472 | ||||||
chr3:100339566
|
A | AT | 6 | a0001c0001t0011g0024a0001c0001t0011g0073a0001c0001t0017g0064others(3): Show | 9 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-239dupT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 100339566 | |||||
chr3:100339577
|
A | T | 3 | a0001c0001t0001g0040a0001c0001t0020g0135a0001c0001t0047g0107 | 4 | HG02572.hp1 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-238A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339577 | ||||||
chr3:100339622
|
C | G | 45 | a0001c0001t0001g0040a0001c0001t0004g0002a0001c0001t0004g0021others(42): Show | 112 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.127-193C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339622 | ||||||
chr3:100339698
|
T | A | 1 | a0001c0001t0004g0042 | 2 | NA18956.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.127-117T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339698 | ||||||
chr3:100339772
|
T | A | 1 | a0001c0001t0002g0036 | 2 | HG01099.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.127-43T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 2/9 | chr3 | 100339772 | ||||||
chr3:100340272
|
C | G | 1 | a0001c0001t0020g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.247+337C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340272 | ||||||
chr3:100340324
|
C | G | 21 | a0001c0001t0005g0006a0001c0001t0005g0012a0001c0001t0005g0025others(18): Show | 44 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.247+389C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340324 | ||||||
chr3:100340391
|
T | C | 10 | a0001c0001t0008g0022a0001c0001t0008g0067a0001c0001t0008g0134others(7): Show | 13 | HG02109.hp2 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.247+456T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340391 | ||||||
chr3:100340590
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.248-483G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340590 | ||||||
chr3:100340623
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.248-450C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340623 | ||||||
chr3:100340644
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.248-429T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340644 | ||||||
chr3:100340674
|
GAATTC | G | 33 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0016others(30): Show | 78 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.248-396_248-392del others(5): Show |
NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 100340674 | |||||
chr3:100340694
|
G | C | 1 | a0001c0001t0001g0109 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.248-379G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340694 | ||||||
chr3:100340714
|
A | G | 2 | a0001c0001t0011g0024a0001c0001t0011g0073 | 4 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-359A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340714 | ||||||
chr3:100340822
|
T | C | 32 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0016others(29): Show | 76 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.248-251T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340822 | ||||||
chr3:100340849
|
T | C | 2 | a0001c0001t0003g0014a0001c0001t0003g0051 | 5 | HG01358.hp1 HG01943.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.248-224T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 3/9 | chr3 | 100340849 | ||||||
chr3:100341250
|
C | T | 1 | a0001c0001t0001g0045 | 2 | NA18970.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.336+89C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341250 | ||||||
chr3:100341291
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 120 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.336+130G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341291 | ||||||
chr3:100341448
|
T | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 120 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.336+287T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341448 | ||||||
chr3:100341637
|
G | A | 1 | a0001c0001t0001g0040 | 2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.336+476G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341637 | ||||||
chr3:100341717
|
G | C | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+556G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341717 | ||||||
chr3:100341724
|
G | T | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+563G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341724 | ||||||
chr3:100341726
|
G | T | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+565G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341726 | ||||||
chr3:100341727
|
T | A | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+566T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341727 | ||||||
chr3:100341729
|
G | T | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+568G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341729 | ||||||
chr3:100341731
|
C | A | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+570C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341731 | ||||||
chr3:100341734
|
C | G | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+573C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341734 | ||||||
chr3:100341735
|
T | A | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+574T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341735 | ||||||
chr3:100341736
|
T | A | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+575T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341736 | ||||||
chr3:100341737
|
T | A | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+576T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341737 | ||||||
chr3:100341741
|
G | C | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+580G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341741 | ||||||
chr3:100341744
|
T | A | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+583T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341744 | ||||||
chr3:100341750
|
G | A | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+589G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341750 | ||||||
chr3:100341752
|
G | A | 1 | a0002c0004t0005g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.336+591G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341752 | ||||||
chr3:100341935
|
C | T | 62 | a0001c0001t0001g0040a0001c0001t0002g0001a0001c0001t0002g0010others(59): Show | 131 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.336+774C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341935 | ||||||
chr3:100341978
|
C | T | 2 | a0001c0001t0003g0030a0001c0001t0003g0059 | 3 | HG02155.hp1 NA18977.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.336+817C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100341978 | ||||||
chr3:100342027
|
A | G | 1 | a0001c0001t0028g0038 | 2 | NA18956.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.336+866A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100342027 | ||||||
chr3:100342177
|
A | G | 1 | a0001c0001t0003g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.336+1016A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100342177 | ||||||
chr3:100342200
|
C | G | 1 | a0001c0001t0003g0029 | 2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.336+1039C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100342200 | ||||||
chr3:100342407
|
A | G | 28 | a0001c0001t0001g0040a0001c0001t0005g0006a0001c0001t0005g0012others(25): Show | 52 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.336+1246A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100342407 | ||||||
chr3:100342519
|
CT | C | 7 | a0001c0001t0003g0030a0001c0001t0003g0059a0001c0001t0008g0022others(4): Show | 11 | HG02109.hp2 HG02155.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.336+1371delT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 100342519 | |||||
chr3:100342897
|
A | G | 1 | a0001c0001t0002g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.336+1736A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100342897 | ||||||
chr3:100342946
|
A | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0046others(14): Show | 53 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.336+1785A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100342946 | ||||||
chr3:100343001
|
A | G | 14 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0043others(11): Show | 22 | HG00423.hp1 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.336+1840A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343001 | ||||||
chr3:100343062
|
T | C | 1 | a0001c0001t0005g0025 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.336+1901T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343062 | ||||||
chr3:100343084
|
A | G | 1 | a0001c0001t0032g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.336+1923A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343084 | ||||||
chr3:100343096
|
T | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0070a0001c0001t0035g0069others(2): Show | 8 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.336+1935T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343096 | ||||||
chr3:100343105
|
G | A | 5 | a0001c0001t0008g0022a0001c0001t0008g0067a0001c0001t0008g0134others(2): Show | 8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.336+1944G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343105 | ||||||
chr3:100343253
|
C | G | 1 | a0001c0001t0020g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.336+2092C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343253 | ||||||
chr3:100343363
|
C | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 111 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.336+2202C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343363 | ||||||
chr3:100343407
|
T | A | 22 | a0001c0001t0002g0072a0001c0001t0004g0002a0001c0001t0004g0021others(19): Show | 65 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.337-2178T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343407 | ||||||
chr3:100343482
|
C | T | 1 | a0001c0001t0026g0037 | 2 | HG01123.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.337-2103C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343482 | ||||||
chr3:100343483
|
G | A | 1 | a0001c0001t0005g0093 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.337-2102G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343483 | ||||||
chr3:100343606
|
C | T | 1 | a0001c0001t0020g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.337-1979C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343606 | ||||||
chr3:100343785
|
G | A | 2 | a0001c0002t0019g0023a0001c0002t0031g0023 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.337-1800G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343785 | ||||||
chr3:100343934
|
G | T | 1 | a0001c0001t0001g0123 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.337-1651G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100343934 | ||||||
chr3:100344008
|
T | A | 1 | a0001c0001t0020g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.337-1577T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344008 | ||||||
chr3:100344267
|
G | A | 1 | a0001c0001t0047g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.337-1318G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344267 | ||||||
chr3:100344285
|
A | G | 1 | a0001c0001t0003g0057 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.337-1300A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344285 | ||||||
chr3:100344296
|
C | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0117a0001c0001t0009g0013others(1): Show | 6 | HG00423.hp1 HG02027.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-1289C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344296 | ||||||
chr3:100344327
|
G | T | 1 | a0001c0001t0003g0124 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.337-1258G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344327 | ||||||
chr3:100344533
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.337-1052C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344533 | ||||||
chr3:100344557
|
T | A | 1 | a0001c0001t0020g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.337-1028T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344557 | ||||||
chr3:100344642
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.337-943C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344642 | ||||||
chr3:100344667
|
A | G | 1 | a0001c0001t0004g0106 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.337-918A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344667 | ||||||
chr3:100344685
|
G | A | 21 | a0001c0001t0004g0002a0001c0001t0004g0021a0001c0001t0004g0031others(18): Show | 64 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.337-900G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344685 | ||||||
chr3:100344851
|
G | C | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.337-734G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344851 | ||||||
chr3:100344901
|
C | T | 1 | a0001c0001t0010g0105 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.337-684C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344901 | ||||||
chr3:100344911
|
C | T | 1 | a0001c0001t0002g0090 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.337-674C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344911 | ||||||
chr3:100344959
|
C | T | 2 | a0001c0001t0006g0018a0001c0001t0006g0104 | 5 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.337-626C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344959 | ||||||
chr3:100344959
|
CT | C | 138 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 317 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(314): Show |
intron_variant | MODIFIER | c.337-615delT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 100344959 | |||||
chr3:100344960
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0006g0018a0001c0001t0006g0104 | 6 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-625T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100344960 | ||||||
chr3:100345050
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.337-535G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345050 | ||||||
chr3:100345101
|
C | T | 1 | a0001c0001t0048g0130 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.337-484C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345101 | ||||||
chr3:100345161
|
T | G | 85 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(82): Show | 193 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.337-424T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345161 | ||||||
chr3:100345210
|
C | T | 4 | a0001c0001t0011g0024a0001c0001t0011g0073a0001c0001t0017g0064others(1): Show | 6 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-375C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345210 | ||||||
chr3:100345254
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.337-331C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345254 | ||||||
chr3:100345383
|
A | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0070a0001c0001t0035g0069others(2): Show | 8 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.337-202A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345383 | ||||||
chr3:100345439
|
G | T | 1 | a0001c0001t0051g0055 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.337-146G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 4/9 | chr3 | 100345439 | ||||||
chr3:100345758
|
G | A | 5 | a0001c0001t0002g0036a0001c0001t0011g0024a0001c0001t0011g0073others(2): Show | 8 | HG01099.hp1 HG01243.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+80G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 5/9 | chr3 | 100345758 | ||||||
chr3:100345897
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 192 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.430+219C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 5/9 | chr3 | 100345897 | ||||||
chr3:100345985
|
C | G | 32 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0016others(29): Show | 76 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.431-196C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 5/9 | chr3 | 100345985 | ||||||
chr3:100346058
|
C | T | 31 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0016others(28): Show | 75 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.431-123C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 5/9 | chr3 | 100346058 | ||||||
chr3:100346401
|
G | A | 2 | a0001c0001t0020g0074a0001c0001t0020g0135 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.505+146G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346401 | ||||||
chr3:100346454
|
T | A | 2 | a0001c0001t0001g0026a0001c0001t0042g0026 | 3 | HG01346.hp1 HG01358.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.505+199T>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346454 | ||||||
chr3:100346698
|
T | G | 1 | a0001c0001t0001g0046 | 2 | NA18978.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.505+443T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346698 | ||||||
chr3:100346733
|
C | G | 22 | a0001c0001t0002g0072a0001c0001t0004g0002a0001c0001t0004g0021others(19): Show | 65 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.505+478C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346733 | ||||||
chr3:100346788
|
G | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 195 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.505+533G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346788 | ||||||
chr3:100346936
|
TG | T | 1 | a0001c0001t0006g0018 | 4 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+684delG | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 100346936 | |||||
chr3:100346982
|
C | G | 142 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(139): Show | 324 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(321): Show |
intron_variant | MODIFIER | c.505+727C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346982 | ||||||
chr3:100346995
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.505+740C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100346995 | ||||||
chr3:100347039
|
T | C | 3 | a0001c0001t0008g0022a0001c0001t0008g0067a0001c0001t0008g0134 | 5 | HG02109.hp2 HG02630.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.505+784T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347039 | ||||||
chr3:100347061
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.505+806T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347061 | ||||||
chr3:100347089
|
G | T | 1 | a0001c0001t0001g0044 | 2 | HG02083.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.505+834G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347089 | ||||||
chr3:100347109
|
T | G | 1 | a0001c0001t0035g0069 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.505+854T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347109 | ||||||
chr3:100347385
|
C | T | 1 | a0001c0001t0003g0124 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.505+1130C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347385 | ||||||
chr3:100347647
|
C | T | 3 | a0001c0001t0003g0028a0001c0001t0003g0054a0001c0001t0058g0028 | 3 | HG00280.hp1 HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.506-1156C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347647 | ||||||
chr3:100347731
|
A | T | 1 | a0001c0001t0002g0036 | 2 | HG01099.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.506-1072A>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347731 | ||||||
chr3:100347784
|
G | T | 17 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0028others(14): Show | 42 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.506-1019G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347784 | ||||||
chr3:100347860
|
C | T | 1 | a0001c0001t0061g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.506-943C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347860 | ||||||
chr3:100347897
|
C | CT | 5 | a0001c0001t0002g0084a0001c0001t0011g0024a0001c0001t0011g0073others(2): Show | 7 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.506-895dupT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 100347897 | |||||
chr3:100347937
|
C | G | 1 | a0001c0001t0008g0067 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.506-866C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347937 | ||||||
chr3:100347953
|
C | T | 2 | a0001c0001t0002g0016a0001c0001t0018g0016 | 4 | NA18955.hp2 NA18962.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.506-850C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347953 | ||||||
chr3:100347954
|
G | A | 2 | a0001c0001t0034g0129a0001c0001t0048g0130 | 2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.506-849G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100347954 | ||||||
chr3:100348013
|
C | T | 2 | a0001c0002t0019g0023a0001c0002t0031g0023 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.506-790C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348013 | ||||||
chr3:100348036
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.506-767G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348036 | ||||||
chr3:100348089
|
A | C | 1 | a0001c0001t0020g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.506-714A>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348089 | ||||||
chr3:100348125
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.506-678C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348125 | ||||||
chr3:100348143
|
C | T | 5 | a0001c0001t0012g0131a0001c0001t0012g0132a0001c0001t0012g0133others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.506-660C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348143 | ||||||
chr3:100348312
|
A | C | 1 | a0001c0001t0006g0017 | 4 | HG01106.hp1 HG02257.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.506-491A>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348312 | ||||||
chr3:100348533
|
G | A | 1 | a0001c0001t0010g0105 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.506-270G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348533 | ||||||
chr3:100348624
|
C | T | 143 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(140): Show | 325 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.506-179C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 6/9 | chr3 | 100348624 | ||||||
chr3:100348927
|
G | A | 2 | a0001c0001t0011g0024a0001c0001t0011g0073 | 4 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.584+46G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100348927 | ||||||
chr3:100348957
|
C | T | 2 | a0001c0001t0034g0129a0001c0001t0048g0130 | 2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.584+76C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100348957 | ||||||
chr3:100349053
|
C | T | 1 | a0001c0001t0046g0068 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.584+172C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100349053 | ||||||
chr3:100349108
|
C | CT | 9 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0004g0060others(6): Show | 12 | HG02027.hp1 HG02135.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.584+245dupT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 100349108 | |||||
chr3:100349192
|
C | T | 1 | a0001c0001t0005g0098 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.584+311C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100349192 | ||||||
chr3:100349954
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.584+1073A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100349954 | ||||||
chr3:100349962
|
A | G | 1 | a0001c0001t0002g0083 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.584+1081A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100349962 | ||||||
chr3:100350414
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.584+1533G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350414 | ||||||
chr3:100350593
|
T | C | 1 | a0001c0001t0004g0100 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.584+1712T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350593 | ||||||
chr3:100350596
|
G | A | 2 | a0001c0002t0019g0023a0001c0002t0031g0023 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.584+1715G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350596 | ||||||
chr3:100350784
|
C | T | 1 | a0001c0001t0012g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.585-1620C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350784 | ||||||
chr3:100350848
|
T | C | 145 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(142): Show | 328 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(325): Show |
intron_variant | MODIFIER | c.585-1556T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350848 | ||||||
chr3:100350855
|
C | G | 50 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 115 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.585-1549C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350855 | ||||||
chr3:100350900
|
C | T | 5 | a0001c0001t0008g0022a0001c0001t0008g0067a0001c0001t0008g0134others(2): Show | 8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.585-1504C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350900 | ||||||
chr3:100350918
|
C | T | 2 | a0001c0002t0019g0023a0001c0002t0031g0023 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.585-1486C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350918 | ||||||
chr3:100350934
|
C | T | 1 | a0001c0001t0001g0047 | 2 | HG00597.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.585-1470C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350934 | ||||||
chr3:100350939
|
G | A | 1 | a0001c0001t0020g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.585-1465G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100350939 | ||||||
chr3:100351174
|
C | T | 5 | a0001c0001t0012g0131a0001c0001t0012g0132a0001c0001t0012g0133others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.585-1230C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351174 | ||||||
chr3:100351200
|
A | G | 3 | a0001c0001t0005g0012a0001c0001t0005g0097a0002c0004t0005g0092 | 7 | NA18940.hp2 NA18953.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.585-1204A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351200 | ||||||
chr3:100351220
|
C | A | 1 | a0001c0001t0004g0101 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.585-1184C>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351220 | ||||||
chr3:100351418
|
A | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0043others(13): Show | 25 | HG00423.hp1 HG00642.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.585-986A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351418 | ||||||
chr3:100351452
|
G | A | 1 | a0001c0001t0044g0102 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.585-952G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351452 | ||||||
chr3:100351620
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.585-784A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351620 | ||||||
chr3:100351846
|
C | T | 1 | a0001c0001t0003g0054 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.585-558C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351846 | ||||||
chr3:100351847
|
G | A | 21 | a0001c0001t0004g0002a0001c0001t0004g0021a0001c0001t0004g0031others(18): Show | 64 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.585-557G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351847 | ||||||
chr3:100351884
|
T | C | 1 | a0001c0001t0003g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.585-520T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351884 | ||||||
chr3:100351901
|
C | T | 50 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 115 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.585-503C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351901 | ||||||
chr3:100351911
|
A | C | 1 | a0001c0001t0030g0082 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.585-493A>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351911 | ||||||
chr3:100351912
|
G | T | 1 | a0001c0001t0001g0115 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.585-492G>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100351912 | ||||||
chr3:100352022
|
G | C | 106 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(103): Show | 241 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.585-382G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100352022 | ||||||
chr3:100352226
|
G | C | 33 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0016others(30): Show | 77 | HG00140.hp2 HG00438.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.585-178G>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100352226 | ||||||
chr3:100352310
|
T | C | 1 | a0001c0001t0005g0094 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.585-94T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100352310 | ||||||
chr3:100352372
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 18 | HG00544.hp1 HG00558.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.585-32C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 7/9 | chr3 | 100352372 | ||||||
chr3:100352938
|
A | G | 1 | a0001c0001t0020g0074 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.683+436A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100352938 | ||||||
chr3:100353191
|
G | A | 2 | a0001c0002t0019g0023a0001c0002t0031g0023 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.683+689G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100353191 | ||||||
chr3:100353392
|
C | T | 2 | a0001c0001t0005g0094a0001c0001t0005g0096 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.683+890C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100353392 | ||||||
chr3:100353488
|
G | A | 51 | a0001c0001t0004g0002a0001c0001t0004g0021a0001c0001t0004g0031others(48): Show | 120 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.683+986G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100353488 | ||||||
chr3:100353601
|
T | G | 2 | a0001c0002t0019g0023a0001c0002t0031g0023 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.683+1099T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100353601 | ||||||
chr3:100353765
|
AGTTTC | A | 5 | a0001c0001t0008g0022a0001c0001t0008g0067a0001c0001t0008g0134others(2): Show | 8 | HG02109.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.684-1006_684-1002d others(7): Show |
NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100353765 | ||||||
chr3:100353777
|
C | CT | 140 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 319 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.684-981dupT | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 100353777 | |||||
chr3:100354051
|
C | T | 1 | a0001c0001t0061g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.684-721C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100354051 | ||||||
chr3:100354197
|
C | T | 1 | a0001c0001t0020g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.684-575C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100354197 | ||||||
chr3:100354418
|
T | C | 1 | a0001c0001t0005g0095 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.684-354T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100354418 | ||||||
chr3:100354489
|
C | T | 17 | a0001c0001t0005g0006a0001c0001t0005g0012a0001c0001t0005g0025others(14): Show | 38 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.684-283C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100354489 | ||||||
chr3:100354633
|
C | T | 1 | a0001c0001t0038g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.684-139C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100354633 | ||||||
chr3:100354737
|
G | A | 4 | a0001c0001t0020g0074a0001c0001t0020g0135a0001c0002t0019g0023others(1): Show | 5 | HG02572.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.684-35G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 8/9 | chr3 | 100354737 | ||||||
chr3:100354880
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.739+53G>A | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100354880 | ||||||
chr3:100354881
|
C | G | 22 | a0001c0001t0004g0002a0001c0001t0004g0021a0001c0001t0004g0031others(19): Show | 65 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.739+54C>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100354881 | ||||||
chr3:100354939
|
C | T | 1 | a0001c0001t0003g0053 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.739+112C>T | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100354939 | ||||||
chr3:100354982
|
T | G | 143 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(140): Show | 325 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.739+155T>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100354982 | ||||||
chr3:100355048
|
A | G | 1 | a0001c0001t0005g0097 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.740-129A>G | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100355048 | ||||||
chr3:100355062
|
TA | T | 22 | a0001c0001t0004g0002a0001c0001t0004g0021a0001c0001t0004g0031others(19): Show | 65 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.740-114delA | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100355062 | ||||||
chr3:100355097
|
T | C | 1 | a0001c0001t0002g0090 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.740-80T>C | NIT2 | ENSG00000114021.12 | transcript | ENST00000394140.9 | protein_coding | 9/9 | chr3 | 100355097 |