geneid | 3176 |
---|---|
ensemblid | ENSG00000150540.14 |
hgncid | 5028 |
symbol | HNMT |
name | histamine N-methyltransferase |
refseq_nuc | NM_006895.3 |
refseq_prot | NP_008826.1 |
ensembl_nuc | ENST00000280097.5 |
ensembl_prot | ENSP00000280097.3 |
mane_status | MANE Select |
chr | chr2 |
start | 137964473 |
end | 138016364 |
strand | + |
ver | v1.2 |
region | chr2:137964473-138016364 |
region5000 | chr2:137959473-138021364 |
regionname0 | HNMT_chr2_137964473_138016364 |
regionname5000 | HNMT_chr2_137959473_138021364 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 292 | 308 | 85 | 52 | 122 | 9 | 38 | 84 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0002 | 0/0 | 292 | 23 | 0 | 8 | 8 | 1 | 6 | 6 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0003 | 0/0 | 292 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 879 | 306 | 85 | 52 | 120 | 9 | 38 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
c0002 | 0/0 | 879 | 23 | 0 | 8 | 8 | 1 | 6 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
c0003 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
c0004 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
c0005 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2254 | 183 | 37 | 36 | 74 | 8 | 26 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0002 | 0/0 | 2254 | 97 | 15 | 19 | 47 | 2 | 14 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0003 | 0/0 | 2254 | 18 | 18 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0004 | 0/0 | 2254 | 5 | 4 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0005 | 0/0 | 2254 | 3 | 3 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0006 | 0/0 | 2254 | 3 | 3 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0007 | 0/0 | 2254 | 3 | 0 | 0 | 3 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0008 | 0/0 | 2254 | 3 | 0 | 0 | 1 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0009 | 0/0 | 2254 | 2 | 0 | 2 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0010 | 0/0 | 2254 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0011 | 0/0 | 2254 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0012 | 0/0 | 2254 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0013 | 0/0 | 2254 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0014 | 0/0 | 2254 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0015 | 0/0 | 2254 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0016 | 0/0 | 2254 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0017 | 0/0 | 2254 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0018 | 0/0 | 2238 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0019 | 0/0 | 2254 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0020 | 0/0 | 2254 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0021 | 0/0 | 2254 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
t0022 | 0/0 | 2254 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 8 | 0 | 2 | 3 | 1 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0002 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0005 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0006 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0013 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0021 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 879 | 306 | 85 | 52 | 120 | 9 | 38 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0004 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0005 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0002c0002 | 0/0 | 879 | 23 | 0 | 8 | 8 | 1 | 6 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0003c0003 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3132 | 180 | 36 | 36 | 72 | 8 | 26 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0002 | 0/0 | 3132 | 75 | 15 | 11 | 39 | 1 | 9 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0003 | 0/0 | 3132 | 18 | 18 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0004 | 0/0 | 3132 | 5 | 4 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0005 | 0/0 | 3132 | 3 | 3 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0006 | 0/0 | 3132 | 3 | 3 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0007 | 0/0 | 3132 | 3 | 0 | 0 | 3 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0008 | 0/0 | 3132 | 3 | 0 | 0 | 1 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0009 | 0/0 | 3132 | 2 | 0 | 2 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0010 | 0/0 | 3132 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0011 | 0/0 | 3132 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0012 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0013 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0014 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0015 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0016 | 0/0 | 3132 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0017 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0018 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0019 | 0/0 | 3132 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0021 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0001t0022 | 0/0 | 3132 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0004t0001 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0001c0005t0001 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0002c0002t0002 | 0/0 | 3132 | 22 | 0 | 8 | 8 | 1 | 5 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0002c0002t0020 | 0/0 | 3132 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
a0003c0003t0001 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | copy fasta | chr2 | 137959473 | 138021364 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 8 | 0 | 2 | 3 | 1 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0002 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0013 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0006 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0008g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0009g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0010g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0010g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0011g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0011g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0012g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0013g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0014g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0015g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0016g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0017g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0018g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0019g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0021g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0001t0022g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0001c0005t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0002c0002t0020g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
a0003c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | GBR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0101 | EUR | FIN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00423 | hp1 | a0001 | c0001 | t0017 | g0225 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0237 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01167 | hp2 | a0001 | c0001 | t0009 | g0009 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01169 | hp2 | a0001 | c0001 | t0009 | g0009 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0234 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0272 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01361 | hp2 | a0001 | c0001 | t0019 | g0195 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | IBS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0069 | EUR | IBS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0271 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0158 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0030 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0049 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02074 | hp1 | a0001 | c0001 | t0011 | g0080 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02135 | hp2 | a0001 | c0001 | t0011 | g0005 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02145 | hp1 | a0003 | c0003 | t0001 | g0262 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | CDX | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02165 | hp1 | a0001 | c0001 | t0008 | g0210 | EAS | CDX | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02257 | hp2 | a0001 | c0001 | t0013 | g0145 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02300 | hp1 | a0001 | c0001 | t0022 | g0115 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02683 | hp2 | a0002 | c0002 | t0020 | g0016 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02698 | hp2 | a0001 | c0001 | t0008 | g0184 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02717 | hp1 | a0001 | c0001 | t0015 | g0266 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02965 | hp1 | a0001 | c0001 | t0021 | g0265 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02970 | hp1 | a0001 | c0001 | t0012 | g0055 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0031 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03491 | hp1 | a0001 | c0001 | t0008 | g0182 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0031 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0016 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03942 | hp1 | a0001 | c0001 | t0016 | g0097 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0132 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0127 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | CHB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | YRI | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18974 | hp1 | a0001 | c0001 | t0007 | g0139 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18977 | hp1 | a0001 | c0001 | t0007 | g0077 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18985 | hp1 | a0001 | c0004 | t0001 | g0202 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18986 | hp2 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19002 | hp2 | a0001 | c0001 | t0014 | g0252 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | LWK | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | LWK | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19055 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19055 | hp2 | a0001 | c0005 | t0001 | g0212 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19066 | hp1 | a0001 | c0001 | t0018 | g0007 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ASW | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ASW | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | TSI | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | TSI | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0047 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | USA | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
HG06807 | hp2 | a0001 | c0001 | t0010 | g0156 | AFR | USA | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | USA | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | USA | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
NA21309 | hp2 | a0001 | c0001 | t0010 | g0155 | AFR | LWK | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0057 | REF | REF | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:138000972
|
G | A | 1 | a0003 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.245G>A | p.Cys82Tyr | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/6 | 264/3132 | 245/879 | 82/292 | chr2 | 138000972 | ||
chr2:138002079
|
C | T | 1 | a0002 | 23 | HG00280.hp1 HG00558.hp2 HG01070.hp1 others(20): Show |
missense_variant | MODERATE | c.314C>T | p.Thr105Ile | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/6 | 333/3132 | 314/879 | 105/292 | chr2 | 138002079 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:138013809
|
C | T | 1 | a0001c0005 | 1 | NA19055.hp2 | synonymous_variant | LOW | c.558C>T | p.Tyr186Tyr | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 577/3132 | 558/879 | 186/292 | chr2 | 138013809 | ||
chr2:138013926
|
T | C | 1 | a0001c0004 | 1 | NA18985.hp1 | synonymous_variant | LOW | c.675T>C | p.Asp225Asp | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 694/3132 | 675/879 | 225/292 | chr2 | 138013926 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:138014165
|
T | C | 1 | a0001c0001t0009 | 2 | HG01167.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*35T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 35 | chr2 | 138014165 | |||||
chr2:138014190
|
A | G | 9 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(6): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*60A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 60 | chr2 | 138014190 | |||||
chr2:138014348
|
A | T | 9 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(6): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*218A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 218 | chr2 | 138014348 | |||||
chr2:138014640
|
A | G | 1 | a0001c0001t0011 | 2 | HG02074.hp1 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*510A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 510 | chr2 | 138014640 | |||||
chr2:138014765
|
G | C | 1 | a0001c0001t0010 | 2 | HG06807.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*635G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 635 | chr2 | 138014765 | |||||
chr2:138014966
|
C | T | 1 | a0001c0001t0007 | 3 | NA18974.hp1 NA18977.hp1 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*836C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 836 | chr2 | 138014966 | |||||
chr2:138014971
|
TTTATTGA others(9): Show |
T | 1 | a0001c0001t0018 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*842_*857delTTATTG others(10): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 842 | chr2 | 138014971 | |||||
chr2:138015124
|
C | T | 9 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(6): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*994C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 994 | chr2 | 138015124 | |||||
chr2:138015139
|
T | G | 1 | a0001c0001t0012 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1009T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1009 | chr2 | 138015139 | |||||
chr2:138015168
|
G | C | 2 | a0001c0001t0004a0001c0001t0010 | 7 | HG00735.hp1 HG02809.hp1 HG03130.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1038G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1038 | chr2 | 138015168 | |||||
chr2:138015169
|
T | G | 1 | a0001c0001t0008 | 3 | HG02165.hp1 HG02698.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1039T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1039 | chr2 | 138015169 | |||||
chr2:138015331
|
A | G | 1 | a0001c0001t0017 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1201A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1201 | chr2 | 138015331 | |||||
chr2:138015412
|
G | A | 1 | a0001c0001t0013 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1282G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1282 | chr2 | 138015412 | |||||
chr2:138015418
|
G | A | 1 | a0001c0001t0019 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1288G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1288 | chr2 | 138015418 | |||||
chr2:138015432
|
A | G | 1 | a0001c0001t0016 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1302A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1302 | chr2 | 138015432 | |||||
chr2:138015492
|
G | A | 1 | a0001c0001t0005 | 3 | HG02258.hp2 HG02486.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1362G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1362 | chr2 | 138015492 | |||||
chr2:138015524
|
T | C | 1 | a0002c0002t0020 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1394T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1394 | chr2 | 138015524 | |||||
chr2:138015559
|
T | C | 1 | a0001c0001t0021 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1429T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1429 | chr2 | 138015559 | |||||
chr2:138015659
|
G | A | 9 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(6): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1529G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1529 | chr2 | 138015659 | |||||
chr2:138015752
|
C | T | 1 | a0001c0001t0022 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1622C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1622 | chr2 | 138015752 | |||||
chr2:138015899
|
G | A | 1 | a0001c0001t0014 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1769G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1769 | chr2 | 138015899 | |||||
chr2:138015899
|
G | T | 1 | a0001c0001t0006 | 3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1769G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1769 | chr2 | 138015899 | |||||
chr2:138016022
|
G | A | 1 | a0001c0001t0015 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1892G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1892 | chr2 | 138016022 | |||||
chr2:138016068
|
C | T | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(13): Show | 140 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*1938C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1938 | chr2 | 138016068 | |||||
chr2:138016113
|
C | T | 1 | a0001c0001t0006 | 3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1983C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1983 | chr2 | 138016113 | |||||
chr2:138016182
|
T | C | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(13): Show | 140 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*2052T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 2052 | chr2 | 138016182 | |||||
chr2:138016241
|
C | G | 9 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(6): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2111C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 2111 | chr2 | 138016241 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:137964770
|
C | T | 1 | a0001c0001t0005g0032 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.137+142C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137964770 | ||||||
chr2:137964813
|
G | A | 1 | a0001c0001t0005g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137+185G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137964813 | ||||||
chr2:137965033
|
C | A | 1 | a0001c0001t0003g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.137+405C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965033 | ||||||
chr2:137965170
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.137+542G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965170 | ||||||
chr2:137965179
|
A | T | 1 | a0002c0002t0002g0031 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.137+551A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965179 | ||||||
chr2:137965242
|
C | CT | 14 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0002g0007others(11): Show | 18 | HG00558.hp2 HG01346.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.137+622dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 137965242 | |||||
chr2:137965284
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.137+656G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965284 | ||||||
chr2:137965505
|
A | G | 5 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0015g0266others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+877A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965505 | ||||||
chr2:137965516
|
G | A | 1 | a0001c0001t0009g0009 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.137+888G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965516 | ||||||
chr2:137965674
|
A | G | 5 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0015g0266others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+1046A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965674 | ||||||
chr2:137965718
|
T | C | 5 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+1090T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965718 | ||||||
chr2:137965826
|
C | T | 1 | a0001c0001t0003g0028 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.137+1198C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965826 | ||||||
chr2:137966043
|
G | C | 5 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0015g0266others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+1415G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137966043 | ||||||
chr2:137966318
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.137+1690C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137966318 | ||||||
chr2:137966416
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.137+1788C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137966416 | ||||||
chr2:137966528
|
A | T | 1 | a0001c0001t0001g0259 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.137+1900A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137966528 | ||||||
chr2:137966766
|
G | GT | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0020others(123): Show | 148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.137+2140dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 137966766 | |||||
chr2:137966787
|
A | G | 3 | a0001c0001t0001g0157a0002c0002t0002g0019a0002c0002t0002g0158 | 4 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+2159A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137966787 | ||||||
chr2:137967011
|
T | C | 5 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0015g0266others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+2383T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967011 | ||||||
chr2:137967168
|
C | T | 3 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258 | 3 | HG01928.hp1 HG01943.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.137+2540C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967168 | ||||||
chr2:137967176
|
T | A | 5 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0015g0266others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+2548T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967176 | ||||||
chr2:137967181
|
C | T | 2 | a0001c0001t0010g0155a0001c0001t0010g0156 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.137+2553C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967181 | ||||||
chr2:137967182
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG01243.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+2554G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967182 | ||||||
chr2:137967432
|
C | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.138-2733C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967432 | ||||||
chr2:137967526
|
A | G | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02647.hp2 HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.138-2639A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967526 | ||||||
chr2:137967546
|
T | C | 2 | a0001c0001t0003g0061a0001c0001t0003g0062 | 2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.138-2619T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967546 | ||||||
chr2:137967608
|
T | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-2557T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967608 | ||||||
chr2:137967632
|
C | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.138-2533C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967632 | ||||||
chr2:137967762
|
G | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.138-2403G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967762 | ||||||
chr2:137968041
|
G | A | 1 | a0001c0001t0003g0067 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.138-2124G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968041 | ||||||
chr2:137968227
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.138-1938T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968227 | ||||||
chr2:137968310
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.138-1855G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968310 | ||||||
chr2:137968327
|
A | C | 2 | a0001c0001t0003g0061a0001c0001t0003g0062 | 2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.138-1838A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968327 | ||||||
chr2:137968386
|
C | T | 1 | a0001c0001t0003g0067 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.138-1779C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968386 | ||||||
chr2:137968421
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.138-1744G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968421 | ||||||
chr2:137968627
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.138-1538C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968627 | ||||||
chr2:137968712
|
G | T | 7 | a0001c0001t0001g0151a0001c0001t0002g0018a0001c0001t0002g0152others(4): Show | 8 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-1453G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968712 | ||||||
chr2:137968785
|
C | T | 1 | a0001c0001t0005g0032 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.138-1380C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968785 | ||||||
chr2:137968944
|
T | G | 5 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0015g0266others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-1221T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968944 | ||||||
chr2:137968972
|
C | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.138-1193C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968972 | ||||||
chr2:137969045
|
T | C | 1 | a0001c0001t0003g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.138-1120T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969045 | ||||||
chr2:137969063
|
A | G | 3 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258 | 3 | HG01928.hp1 HG01943.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.138-1102A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969063 | ||||||
chr2:137969202
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.138-963C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969202 | ||||||
chr2:137969262
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.138-903A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969262 | ||||||
chr2:137969326
|
C | G | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG01074.hp1 HG01074.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.138-839C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969326 | ||||||
chr2:137969417
|
G | A | 1 | a0001c0001t0005g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.138-748G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969417 | ||||||
chr2:137969627
|
C | T | 1 | a0001c0001t0015g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.138-538C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969627 | ||||||
chr2:137969630
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.138-535G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969630 | ||||||
chr2:137969766
|
A | G | 1 | a0001c0001t0005g0032 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.138-399A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969766 | ||||||
chr2:137969903
|
C | T | 3 | a0001c0001t0004g0017a0001c0001t0004g0144a0001c0001t0013g0145 | 4 | HG02257.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-262C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969903 | ||||||
chr2:137969971
|
T | C | 1 | a0003c0003t0001g0262 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.138-194T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969971 | ||||||
chr2:137970037
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.138-128G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137970037 | ||||||
chr2:137970597
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.190+380A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970597 | ||||||
chr2:137970605
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.190+388T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970605 | ||||||
chr2:137970641
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0014g0252 | 2 | HG02040.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.190+424C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970641 | ||||||
chr2:137970644
|
G | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 6 | HG01081.hp2 HG01256.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.190+427G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970644 | ||||||
chr2:137970654
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.190+437C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970654 | ||||||
chr2:137970691
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.190+474G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970691 | ||||||
chr2:137970696
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.190+479G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970696 | ||||||
chr2:137970781
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG01243.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+564G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970781 | ||||||
chr2:137970796
|
T | G | 1 | a0001c0001t0002g0163 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.190+579T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970796 | ||||||
chr2:137970827
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.190+610G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970827 | ||||||
chr2:137970828
|
G | A | 24 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(21): Show | 28 | HG00558.hp2 HG01167.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.190+611G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970828 | ||||||
chr2:137970906
|
C | A | 1 | a0001c0001t0003g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+689C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970906 | ||||||
chr2:137970931
|
AAAAAAGA others(7): Show |
A | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.190+718_190+731del others(14): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970931 | |||||
chr2:137970933
|
A | AAAAAAGA others(7): Show |
1 | a0001c0001t0003g0076 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.190+719_190+720ins others(14): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970933 | |||||
chr2:137970933
|
AAAAG | A | 6 | a0001c0001t0001g0151a0001c0001t0002g0018a0001c0001t0002g0152others(3): Show | 8 | HG02155.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.190+752_190+755del others(4): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970933 | |||||
chr2:137970933
|
AAAAGAAA others(1): Show |
A | 87 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(84): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.190+748_190+755del others(8): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970933 | |||||
chr2:137970933
|
AAAAGAAA others(5): Show |
A | 14 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(11): Show | 14 | HG02145.hp2 HG02647.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.190+744_190+755del others(12): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970933 | |||||
chr2:137970934
|
AAAGAAAG | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0078a0001c0001t0001g0079others(11): Show | 18 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.190+720_190+726del others(7): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970934 | |||||
chr2:137970934
|
AAAGAAAG others(4): Show |
A | 4 | a0001c0001t0001g0249a0001c0001t0006g0047a0001c0001t0006g0048others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+720_190+730del others(11): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970934 | |||||
chr2:137970934
|
AAAGAAAG others(8): Show |
A | 1 | a0001c0001t0001g0248 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.190+720_190+734del others(15): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970934 | |||||
chr2:137970935
|
AAGAAAGA others(3): Show |
A | 7 | a0001c0001t0001g0066a0001c0001t0002g0173a0001c0001t0002g0264others(4): Show | 7 | HG02145.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.190+720_190+729del others(10): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970935 | |||||
chr2:137970935
|
AAGAAAGA others(7): Show |
A | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0020others(118): Show | 142 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.190+720_190+733del others(14): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970935 | |||||
chr2:137970935
|
AAGAAAGA others(11): Show |
A | 1 | a0001c0001t0001g0180 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.190+720_190+737del others(18): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970935 | |||||
chr2:137970936
|
AGAAAGAA others(2): Show |
A | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+720_190+728del others(9): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970936 | ||||||
chr2:137970936
|
AGAAAGAA others(6): Show |
A | 8 | a0001c0001t0001g0021a0001c0001t0001g0164a0001c0001t0001g0175others(5): Show | 9 | HG00140.hp1 HG01257.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.190+720_190+732del others(13): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970936 | ||||||
chr2:137970945
|
G | A | 3 | a0001c0001t0002g0071a0001c0001t0003g0070a0001c0001t0003g0072 | 3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.190+728G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970945 | ||||||
chr2:137970949
|
G | A | 21 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(18): Show | 21 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.190+732G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970949 | ||||||
chr2:137970965
|
G | A | 1 | a0001c0001t0002g0086 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.190+748G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970965 | ||||||
chr2:137971117
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.190+900C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971117 | ||||||
chr2:137971148
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.190+931T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971148 | ||||||
chr2:137971217
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.190+1000G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971217 | ||||||
chr2:137971388
|
C | T | 3 | a0001c0001t0001g0084a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | NA18941.hp2 NA19083.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.190+1171C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971388 | ||||||
chr2:137971439
|
A | G | 1 | a0001c0001t0007g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.190+1222A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971439 | ||||||
chr2:137971543
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0020others(133): Show | 158 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.190+1326G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971543 | ||||||
chr2:137971611
|
G | T | 6 | a0001c0001t0001g0151a0001c0001t0002g0018a0001c0001t0002g0152others(3): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.190+1394G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971611 | ||||||
chr2:137971664
|
G | A | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(249): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.190+1447G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971664 | ||||||
chr2:137971761
|
A | G | 1 | a0001c0001t0002g0008 | 3 | HG02630.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.190+1544A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971761 | ||||||
chr2:137971806
|
TA | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(113): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.190+1590delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971806 | ||||||
chr2:137971880
|
A | G | 1 | a0001c0001t0003g0067 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.190+1663A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971880 | ||||||
chr2:137971934
|
A | G | 1 | a0001c0001t0005g0032 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.190+1717A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971934 | ||||||
chr2:137971966
|
T | C | 3 | a0001c0001t0006g0047a0001c0001t0006g0048a0001c0001t0006g0049 | 3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.190+1749T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971966 | ||||||
chr2:137972057
|
A | C | 1 | a0001c0001t0001g0250 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.190+1840A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972057 | ||||||
chr2:137972135
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG02602.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.190+1918C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972135 | ||||||
chr2:137972136
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.190+1919G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972136 | ||||||
chr2:137972152
|
T | A | 1 | a0001c0001t0003g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+1935T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972152 | ||||||
chr2:137972267
|
G | A | 1 | a0001c0001t0015g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.190+2050G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972267 | ||||||
chr2:137972304
|
C | T | 1 | a0002c0002t0002g0031 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.190+2087C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972304 | ||||||
chr2:137972354
|
C | T | 5 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0015g0266others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+2137C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972354 | ||||||
chr2:137972417
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.190+2200T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972417 | ||||||
chr2:137972419
|
G | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.190+2202G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972419 | ||||||
chr2:137972779
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(112): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.190+2562G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972779 | ||||||
chr2:137972848
|
T | A | 1 | a0001c0001t0003g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+2631T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972848 | ||||||
chr2:137972887
|
C | T | 6 | a0001c0001t0001g0151a0001c0001t0002g0018a0001c0001t0002g0152others(3): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.190+2670C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972887 | ||||||
chr2:137972911
|
A | T | 1 | a0001c0001t0003g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+2694A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972911 | ||||||
chr2:137972913
|
G | A | 1 | a0001c0001t0003g0028 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.190+2696G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972913 | ||||||
chr2:137973024
|
A | T | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | HG02109.hp2 HG02895.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.190+2807A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973024 | ||||||
chr2:137973091
|
A | G | 1 | a0001c0001t0003g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+2874A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973091 | ||||||
chr2:137973105
|
T | A | 5 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0015g0266others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+2888T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973105 | ||||||
chr2:137973219
|
C | T | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | HG02109.hp2 HG02895.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.190+3002C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973219 | ||||||
chr2:137973596
|
A | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG01243.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+3379A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973596 | ||||||
chr2:137973712
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.190+3495A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973712 | ||||||
chr2:137973771
|
G | GT | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0020others(130): Show | 155 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.190+3562dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137973771 | |||||
chr2:137973780
|
G | T | 4 | a0001c0001t0001g0244a0001c0001t0002g0071a0001c0001t0003g0070others(1): Show | 4 | HG01255.hp1 HG02109.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+3563G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973780 | ||||||
chr2:137973781
|
G | T | 1 | a0001c0001t0002g0136 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.190+3564G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973781 | ||||||
chr2:137973872
|
G | A | 1 | a0001c0001t0001g0022 | 2 | NA18979.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.190+3655G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973872 | ||||||
chr2:137973982
|
C | G | 1 | a0001c0001t0001g0243 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.190+3765C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973982 | ||||||
chr2:137974065
|
C | CAAGATTT others(40): Show |
1 | a0001c0001t0001g0243 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.190+3849_190+3850i others(49): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137974065 | |||||
chr2:137974067
|
T | A | 1 | a0001c0001t0001g0243 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.190+3850T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974067 | ||||||
chr2:137974195
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 35 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.190+3978G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974195 | ||||||
chr2:137974353
|
A | G | 4 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0021g0265others(1): Show | 4 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+4136A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974353 | ||||||
chr2:137974573
|
G | A | 1 | a0001c0001t0005g0032 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.190+4356G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974573 | ||||||
chr2:137974606
|
A | C | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+4389A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974606 | ||||||
chr2:137974624
|
G | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.190+4407G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974624 | ||||||
chr2:137974711
|
C | G | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(249): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.190+4494C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974711 | ||||||
chr2:137974778
|
G | T | 5 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0015g0266others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+4561G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974778 | ||||||
chr2:137974848
|
C | A | 3 | a0001c0001t0002g0071a0001c0001t0003g0070a0001c0001t0003g0072 | 3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.190+4631C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974848 | ||||||
chr2:137974850
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.190+4633C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974850 | ||||||
chr2:137975006
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.190+4789C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137975006 | ||||||
chr2:137975113
|
A | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG01243.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+4896A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137975113 | ||||||
chr2:137975249
|
A | T | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+5032A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137975249 | ||||||
chr2:137975499
|
A | G | 2 | a0001c0001t0001g0251a0001c0001t0014g0252 | 2 | HG02040.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.190+5282A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137975499 | ||||||
chr2:137975514
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.190+5297T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137975514 | ||||||
chr2:137975930
|
G | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.190+5713G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137975930 | ||||||
chr2:137976026
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02074.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.190+5809G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976026 | ||||||
chr2:137976084
|
T | C | 2 | a0001c0001t0003g0061a0001c0001t0003g0062 | 2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.190+5867T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976084 | ||||||
chr2:137976272
|
AC | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 58 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.190+6056delC | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976272 | ||||||
chr2:137976273
|
C | A | 220 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(217): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.190+6056C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976273 | ||||||
chr2:137976280
|
C | A | 20 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(17): Show | 20 | HG00280.hp1 HG00558.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.190+6063C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976280 | ||||||
chr2:137976280
|
CA | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.190+6076delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137976280 | |||||
chr2:137976281
|
A | C | 16 | a0001c0001t0001g0027a0001c0001t0001g0063a0001c0001t0001g0064others(13): Show | 17 | HG00558.hp1 HG01261.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.190+6064A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976281 | ||||||
chr2:137976284
|
A | C | 2 | a0001c0001t0003g0061a0001c0001t0003g0062 | 2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.190+6067A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976284 | ||||||
chr2:137976355
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.190+6138T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976355 | ||||||
chr2:137976404
|
A | G | 3 | a0001c0001t0006g0047a0001c0001t0006g0048a0001c0001t0006g0049 | 3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.190+6187A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976404 | ||||||
chr2:137976546
|
C | T | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+6329C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976546 | ||||||
chr2:137977092
|
T | G | 1 | a0001c0001t0002g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.190+6875T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977092 | ||||||
chr2:137977151
|
T | C | 7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(4): Show | 7 | HG02109.hp2 HG02895.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.190+6934T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977151 | ||||||
chr2:137977239
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.190+7022A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977239 | ||||||
chr2:137977549
|
C | T | 1 | a0001c0001t0003g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+7332C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977549 | ||||||
chr2:137977552
|
C | T | 1 | a0001c0001t0012g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.190+7335C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977552 | ||||||
chr2:137977600
|
T | C | 1 | a0001c0001t0005g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.190+7383T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977600 | ||||||
chr2:137977668
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0191 | 3 | HG02056.hp1 HG02080.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.190+7451A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977668 | ||||||
chr2:137977800
|
C | A | 1 | a0001c0001t0003g0028 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.190+7583C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977800 | ||||||
chr2:137977885
|
T | A | 1 | a0001c0001t0001g0192 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.190+7668T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977885 | ||||||
chr2:137977907
|
T | G | 3 | a0001c0001t0002g0071a0001c0001t0003g0070a0001c0001t0003g0072 | 3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.190+7690T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977907 | ||||||
chr2:137977926
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.190+7709A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977926 | ||||||
chr2:137977945
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02647.hp2 HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.190+7728C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977945 | ||||||
chr2:137978033
|
A | T | 1 | a0001c0001t0001g0243 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.190+7816A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978033 | ||||||
chr2:137978101
|
G | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.190+7884G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978101 | ||||||
chr2:137978172
|
C | T | 1 | a0001c0001t0003g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+7955C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978172 | ||||||
chr2:137978270
|
G | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+8053G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978270 | ||||||
chr2:137978289
|
C | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.190+8072C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978289 | ||||||
chr2:137978300
|
G | A | 9 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0167others(6): Show | 9 | HG01167.hp1 HG01257.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.190+8083G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978300 | ||||||
chr2:137978317
|
TATA | T | 4 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0015g0266others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+8104_190+8106d others(5): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978317 | |||||
chr2:137978340
|
T | C | 3 | a0001c0001t0002g0071a0001c0001t0003g0070a0001c0001t0003g0072 | 3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.190+8123T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978340 | ||||||
chr2:137978382
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.190+8165T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978382 | ||||||
chr2:137978428
|
A | ATATACAA others(25): Show |
3 | a0001c0001t0002g0029a0001c0001t0002g0269a0001c0001t0003g0070 | 4 | HG02523.hp1 HG03486.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+8263_190+8294d others(34): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978428 | |||||
chr2:137978480
|
G | T | 4 | a0001c0001t0001g0157a0001c0001t0013g0145a0002c0002t0002g0019others(1): Show | 5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8263G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978480 | ||||||
chr2:137978491
|
AT | A | 3 | a0001c0001t0001g0157a0002c0002t0002g0019a0002c0002t0002g0158 | 4 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+8276delT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978491 | |||||
chr2:137978510
|
TATATAAT others(86): Show |
T | 1 | a0001c0001t0002g0268 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.190+8356_190+8448d others(95): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978510 | |||||
chr2:137978512
|
T | G | 4 | a0001c0001t0001g0157a0001c0001t0013g0145a0002c0002t0002g0019others(1): Show | 5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8295T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978512 | ||||||
chr2:137978523
|
AT | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(111): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.190+8308delT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978523 | |||||
chr2:137978541
|
T | C | 4 | a0001c0001t0001g0157a0001c0001t0013g0145a0002c0002t0002g0019others(1): Show | 5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8324T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978541 | ||||||
chr2:137978553
|
G | A | 4 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0015g0266others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+8336G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978553 | ||||||
chr2:137978571
|
GACT | G | 4 | a0001c0001t0001g0157a0001c0001t0013g0145a0002c0002t0002g0019others(1): Show | 5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8356_190+8358d others(5): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978571 | |||||
chr2:137978576
|
G | GATAATAT others(22): Show |
3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02647.hp2 HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.190+8389_190+8417d others(31): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978576 | |||||
chr2:137978576
|
G | T | 4 | a0001c0001t0001g0157a0001c0001t0013g0145a0002c0002t0002g0019others(1): Show | 5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8359G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978576 | ||||||
chr2:137978605
|
T | G | 1 | a0001c0001t0002g0268 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.190+8388T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978605 | ||||||
chr2:137978605
|
T | TATAATAT others(25): Show |
1 | a0001c0001t0005g0032 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.190+8400_190+8401i others(34): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978605 | |||||
chr2:137978605
|
T | TATAATAT others(25): Show |
118 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.190+8484_190+8515d others(34): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978605 | |||||
chr2:137978605
|
T | TATAATAT others(57): Show |
126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0020others(123): Show | 149 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.190+8452_190+8515d others(66): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978605 | |||||
chr2:137978605
|
T | TATAATAT others(89): Show |
4 | a0001c0001t0001g0166a0001c0001t0001g0197a0001c0001t0001g0198others(1): Show | 4 | HG01981.hp2 HG03654.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+8420_190+8515d others(98): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978605 | |||||
chr2:137978605
|
T | TATAATAT others(153): Show |
1 | a0001c0001t0001g0196 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.190+8515_190+8516i others(162): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978605 | |||||
chr2:137978605
|
T | TTAG | 4 | a0001c0001t0001g0157a0001c0001t0013g0145a0002c0002t0002g0019others(1): Show | 5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8388_190+8389i others(5): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978605 | ||||||
chr2:137978637
|
G | T | 1 | a0002c0002t0002g0158 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.190+8420G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978637 | ||||||
chr2:137978638
|
A | ATAATATA others(25): Show |
4 | a0001c0001t0003g0028a0001c0001t0006g0047a0001c0001t0006g0048others(1): Show | 5 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+8452_190+8453i others(34): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978638 | |||||
chr2:137978701
|
G | GATAATAT others(57): Show |
2 | a0001c0001t0001g0171a0001c0001t0003g0034 | 2 | HG02922.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.190+8515_190+8516i others(66): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978701 | |||||
chr2:137978701
|
G | GATAATAT others(25): Show |
1 | a0001c0001t0002g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.190+8533_190+8564d others(34): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978701 | |||||
chr2:137978701
|
G | GATAATAT others(57): Show |
2 | a0001c0001t0001g0051a0003c0003t0001g0262 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.190+8501_190+8564d others(66): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978701 | |||||
chr2:137978701
|
G | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02647.hp2 HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.190+8484G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978701 | ||||||
chr2:137978733
|
T | G | 11 | a0001c0001t0001g0091a0001c0001t0001g0199a0001c0001t0002g0071others(8): Show | 11 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.190+8516T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978733 | ||||||
chr2:137978765
|
T | G | 1 | a0001c0001t0002g0088 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.190+8548T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978765 | ||||||
chr2:137978789
|
T | A | 1 | a0001c0001t0002g0083 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.190+8572T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978789 | ||||||
chr2:137978895
|
G | C | 5 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8678G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978895 | ||||||
chr2:137978899
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG00408.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.190+8682A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978899 | ||||||
chr2:137978946
|
T | C | 1 | a0001c0001t0010g0155 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.190+8729T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978946 | ||||||
chr2:137978959
|
A | G | 1 | a0001c0001t0005g0032 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.190+8742A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978959 | ||||||
chr2:137978998
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.190+8781A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978998 | ||||||
chr2:137979100
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.190+8883A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979100 | ||||||
chr2:137979241
|
A | G | 1 | a0003c0003t0001g0262 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.190+9024A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979241 | ||||||
chr2:137979356
|
C | T | 4 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0015g0266others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+9139C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979356 | ||||||
chr2:137979364
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.190+9147G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979364 | ||||||
chr2:137979388
|
A | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.190+9171A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979388 | ||||||
chr2:137979398
|
G | A | 4 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0015g0266others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+9181G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979398 | ||||||
chr2:137979532
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.190+9315G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979532 | ||||||
chr2:137979602
|
T | C | 2 | a0001c0001t0003g0061a0001c0001t0003g0062 | 2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.190+9385T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979602 | ||||||
chr2:137979691
|
C | T | 2 | a0001c0001t0010g0155a0001c0001t0010g0156 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.190+9474C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979691 | ||||||
chr2:137980037
|
G | GT | 31 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(28): Show | 32 | HG00280.hp1 HG00609.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.190+9836dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137980037 | |||||
chr2:137980041
|
T | G | 1 | a0001c0001t0005g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.190+9824T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980041 | ||||||
chr2:137980099
|
G | T | 4 | a0001c0001t0002g0264a0001c0001t0003g0076a0001c0001t0003g0263others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+9882G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980099 | ||||||
chr2:137980258
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.190+10041C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980258 | ||||||
chr2:137980288
|
C | T | 5 | a0001c0001t0002g0264a0001c0001t0003g0076a0001c0001t0003g0263others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+10071C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980288 | ||||||
chr2:137980348
|
T | C | 1 | a0001c0001t0007g0077 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.190+10131T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980348 | ||||||
chr2:137980369
|
AAGAGCAA others(4): Show |
A | 1 | a0001c0001t0001g0099 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.190+10155_190+1016 others(15): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137980369 | |||||
chr2:137980441
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0016g0097 | 2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.190+10224C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980441 | ||||||
chr2:137980442
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.190+10225C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980442 | ||||||
chr2:137980497
|
G | A | 13 | a0001c0001t0001g0177a0001c0001t0001g0193a0001c0001t0001g0200others(10): Show | 13 | HG00099.hp2 HG00140.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.190+10280G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980497 | ||||||
chr2:137980533
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.190+10316T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980533 | ||||||
chr2:137981119
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.190+10902A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981119 | ||||||
chr2:137981190
|
T | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0240a0001c0001t0001g0241 | 3 | HG00408.hp2 NA18949.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.190+10973T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981190 | ||||||
chr2:137981427
|
CCTA | C | 3 | a0001c0001t0002g0264a0001c0001t0003g0263a0001c0001t0021g0265 | 3 | HG02486.hp2 HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.190+11214_190+1121 others(7): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137981427 | |||||
chr2:137981460
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.190+11243C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981460 | ||||||
chr2:137981505
|
G | A | 1 | a0001c0001t0016g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.190+11288G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981505 | ||||||
chr2:137981595
|
G | A | 1 | a0001c0001t0010g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.190+11378G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981595 | ||||||
chr2:137981731
|
C | T | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+11514C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981731 | ||||||
chr2:137981733
|
A | G | 4 | a0001c0001t0004g0017a0001c0001t0004g0144a0001c0001t0004g0236others(1): Show | 5 | HG00735.hp1 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+11516A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981733 | ||||||
chr2:137981821
|
C | T | 1 | a0001c0001t0012g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.190+11604C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981821 | ||||||
chr2:137982118
|
G | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0143 | 3 | HG00621.hp2 HG02129.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.190+11901G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982118 | ||||||
chr2:137982140
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.190+11923C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982140 | ||||||
chr2:137982306
|
T | G | 1 | a0001c0001t0001g0192 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.190+12089T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982306 | ||||||
chr2:137982466
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.190+12249G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982466 | ||||||
chr2:137982487
|
A | T | 2 | a0001c0001t0010g0155a0001c0001t0010g0156 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.190+12270A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982487 | ||||||
chr2:137982510
|
C | T | 10 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(7): Show | 11 | HG00735.hp1 HG02055.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.190+12293C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982510 | ||||||
chr2:137982606
|
T | G | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+12389T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982606 | ||||||
chr2:137982769
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.190+12552C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982769 | ||||||
chr2:137982941
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.190+12724A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982941 | ||||||
chr2:137982974
|
A | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 6 | HG01256.hp2 HG02258.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+12757A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982974 | ||||||
chr2:137983196
|
A | C | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.190+12979A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983196 | ||||||
chr2:137983340
|
A | G | 1 | a0001c0001t0003g0068 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.190+13123A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983340 | ||||||
chr2:137983378
|
T | C | 1 | a0002c0002t0002g0103 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.190+13161T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983378 | ||||||
chr2:137983383
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.190+13166G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983383 | ||||||
chr2:137983468
|
CA | C | 5 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0068others(2): Show | 6 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+13260delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137983468 | |||||
chr2:137983506
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 37 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.190+13289C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983506 | ||||||
chr2:137983525
|
C | G | 8 | a0002c0002t0002g0016a0002c0002t0002g0019a0002c0002t0002g0031others(5): Show | 10 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.190+13308C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983525 | ||||||
chr2:137983568
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.190+13351G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983568 | ||||||
chr2:137983606
|
G | C | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+13389G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983606 | ||||||
chr2:137983613
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.190+13396G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983613 | ||||||
chr2:137983866
|
G | C | 1 | a0001c0001t0001g0256 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.190+13649G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983866 | ||||||
chr2:137984030
|
G | T | 4 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0068others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+13813G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984030 | ||||||
chr2:137984351
|
A | G | 7 | a0001c0001t0002g0050a0001c0001t0002g0071a0001c0001t0002g0173others(4): Show | 7 | HG02572.hp1 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.190+14134A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984351 | ||||||
chr2:137984365
|
G | A | 4 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0068others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+14148G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984365 | ||||||
chr2:137984559
|
T | C | 1 | a0001c0001t0005g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.190+14342T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984559 | ||||||
chr2:137984586
|
A | T | 6 | a0001c0001t0002g0050a0001c0001t0002g0071a0001c0001t0002g0173others(3): Show | 6 | HG02572.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+14369A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984586 | ||||||
chr2:137984650
|
C | T | 1 | a0001c0001t0015g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.190+14433C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984650 | ||||||
chr2:137984651
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.190+14434G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984651 | ||||||
chr2:137984916
|
G | C | 1 | a0001c0001t0001g0246 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.190+14699G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984916 | ||||||
chr2:137985080
|
T | C | 1 | a0001c0001t0005g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.190+14863T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985080 | ||||||
chr2:137985202
|
TA | T | 90 | a0001c0001t0001g0096a0001c0001t0001g0206a0001c0001t0001g0256others(87): Show | 109 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.190+15000delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137985202 | |||||
chr2:137985237
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.190+15020T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985237 | ||||||
chr2:137985245
|
C | T | 1 | a0001c0001t0003g0028 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.190+15028C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985245 | ||||||
chr2:137985334
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.190+15117G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985334 | ||||||
chr2:137985595
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0206 | 2 | NA18939.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.191-15323C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985595 | ||||||
chr2:137985596
|
G | A | 96 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(93): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.191-15322G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985596 | ||||||
chr2:137985657
|
G | A | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-15261G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985657 | ||||||
chr2:137985925
|
C | T | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-14993C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985925 | ||||||
chr2:137985926
|
A | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(266): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.191-14992A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985926 | ||||||
chr2:137986017
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.191-14901A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986017 | ||||||
chr2:137986042
|
T | G | 1 | a0001c0001t0003g0028 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191-14876T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986042 | ||||||
chr2:137986065
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.191-14853G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986065 | ||||||
chr2:137986253
|
T | C | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-14665T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986253 | ||||||
chr2:137986302
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.191-14616A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986302 | ||||||
chr2:137986756
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(134): Show | 166 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.191-14162G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986756 | ||||||
chr2:137986964
|
A | C | 1 | a0001c0001t0003g0028 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191-13954A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986964 | ||||||
chr2:137987574
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(87): Show | 110 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.191-13344G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137987574 | ||||||
chr2:137987601
|
CT | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 148 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.191-13289delT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137987601 | |||||
chr2:137987601
|
CTT | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(118): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.191-13290_191-1328 others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137987601 | |||||
chr2:137987601
|
CTTT | C | 13 | a0001c0001t0001g0075a0001c0001t0001g0147a0001c0001t0001g0186others(10): Show | 13 | HG01074.hp1 HG02074.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.191-13291_191-1328 others(7): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137987601 | |||||
chr2:137987691
|
C | T | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-13227C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137987691 | ||||||
chr2:137987826
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.191-13092C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137987826 | ||||||
chr2:137987943
|
C | T | 3 | a0001c0001t0006g0047a0001c0001t0006g0048a0001c0001t0006g0049 | 3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.191-12975C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137987943 | ||||||
chr2:137988015
|
T | C | 1 | a0001c0001t0012g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.191-12903T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988015 | ||||||
chr2:137988095
|
C | T | 1 | a0001c0001t0003g0041 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.191-12823C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988095 | ||||||
chr2:137988124
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.191-12794G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988124 | ||||||
chr2:137988280
|
G | T | 3 | a0001c0001t0003g0072a0001c0001t0003g0150a0001c0001t0003g0153 | 3 | HG02109.hp2 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.191-12638G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988280 | ||||||
chr2:137988469
|
C | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(29): Show | 41 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.191-12449C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988469 | ||||||
chr2:137988525
|
T | C | 1 | a0002c0002t0002g0272 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.191-12393T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988525 | ||||||
chr2:137988550
|
CT | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(134): Show | 166 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.191-12360delT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137988550 | |||||
chr2:137988745
|
C | T | 5 | a0001c0001t0003g0028a0001c0001t0003g0070a0001c0001t0003g0072others(2): Show | 6 | HG02109.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-12173C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988745 | ||||||
chr2:137988789
|
C | T | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-12129C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988789 | ||||||
chr2:137988829
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(109): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.191-12089T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988829 | ||||||
chr2:137988834
|
C | T | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-12084C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988834 | ||||||
chr2:137988879
|
A | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(135): Show | 168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.191-12039A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988879 | ||||||
chr2:137989205
|
C | A | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-11713C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989205 | ||||||
chr2:137989352
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.191-11566G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989352 | ||||||
chr2:137989586
|
A | G | 1 | a0002c0002t0002g0274 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.191-11332A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989586 | ||||||
chr2:137989634
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.191-11284A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989634 | ||||||
chr2:137989653
|
C | T | 3 | a0001c0001t0002g0018a0001c0001t0002g0152a0001c0001t0002g0154 | 4 | HG02615.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-11265C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989653 | ||||||
chr2:137989698
|
G | T | 12 | a0001c0001t0001g0177a0001c0001t0001g0193a0001c0001t0001g0203others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.191-11220G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989698 | ||||||
chr2:137989756
|
T | C | 2 | a0001c0001t0010g0155a0001c0001t0010g0156 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.191-11162T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989756 | ||||||
chr2:137989771
|
G | A | 2 | a0001c0001t0006g0047a0001c0001t0006g0049 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.191-11147G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989771 | ||||||
chr2:137989837
|
G | T | 4 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0068others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-11081G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989837 | ||||||
chr2:137989953
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0151 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.191-10965G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989953 | ||||||
chr2:137990159
|
G | A | 1 | a0001c0001t0005g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.191-10759G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990159 | ||||||
chr2:137990470
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.191-10448C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990470 | ||||||
chr2:137990493
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.191-10425T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990493 | ||||||
chr2:137990540
|
CT | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0191others(2): Show | 7 | HG02056.hp1 HG02080.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.191-10377delT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990540 | ||||||
chr2:137990559
|
C | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.191-10359C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990559 | ||||||
chr2:137990598
|
T | G | 5 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0068others(2): Show | 5 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.191-10320T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990598 | ||||||
chr2:137990696
|
C | G | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191-10222C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990696 | ||||||
chr2:137990732
|
T | C | 76 | a0001c0001t0001g0084a0001c0001t0002g0004a0001c0001t0002g0005others(73): Show | 94 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.191-10186T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990732 | ||||||
chr2:137990755
|
T | C | 1 | a0001c0001t0003g0028 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191-10163T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990755 | ||||||
chr2:137990793
|
A | T | 1 | a0001c0001t0013g0145 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.191-10125A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990793 | ||||||
chr2:137990876
|
A | G | 5 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0068others(2): Show | 5 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.191-10042A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990876 | ||||||
chr2:137990939
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.191-9979A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990939 | ||||||
chr2:137991108
|
T | A | 1 | a0001c0001t0005g0032 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.191-9810T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991108 | ||||||
chr2:137991176
|
C | T | 3 | a0001c0001t0008g0182a0001c0001t0008g0184a0001c0001t0008g0210 | 3 | HG02165.hp1 HG02698.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.191-9742C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991176 | ||||||
chr2:137991273
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.191-9645G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991273 | ||||||
chr2:137991320
|
T | C | 111 | a0001c0001t0001g0084a0001c0001t0001g0194a0001c0001t0002g0004others(108): Show | 132 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.191-9598T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991320 | ||||||
chr2:137991325
|
A | G | 2 | a0001c0001t0010g0155a0001c0001t0010g0156 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.191-9593A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991325 | ||||||
chr2:137991375
|
A | G | 1 | a0001c0001t0003g0028 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191-9543A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991375 | ||||||
chr2:137991487
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(134): Show | 167 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.191-9431C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991487 | ||||||
chr2:137991692
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.191-9226A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991692 | ||||||
chr2:137991818
|
C | A | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-9100C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991818 | ||||||
chr2:137991819
|
G | A | 1 | a0001c0001t0002g0136 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.191-9099G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991819 | ||||||
chr2:137991834
|
G | A | 2 | a0001c0001t0003g0067a0001c0001t0003g0263 | 2 | HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.191-9084G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991834 | ||||||
chr2:137992013
|
G | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0151 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.191-8905G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992013 | ||||||
chr2:137992014
|
G | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0151 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.191-8904G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992014 | ||||||
chr2:137992015
|
G | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0151 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.191-8903G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992015 | ||||||
chr2:137992016
|
G | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0151 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.191-8902G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992016 | ||||||
chr2:137992017
|
A | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0151 | 2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.191-8901A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992017 | ||||||
chr2:137992024
|
TC | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(128): Show | 160 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.191-8887delC | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137992024 | |||||
chr2:137992106
|
T | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(266): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.191-8812T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992106 | ||||||
chr2:137992176
|
G | C | 1 | a0001c0001t0003g0039 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.191-8742G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992176 | ||||||
chr2:137992770
|
G | C | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.191-8148G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992770 | ||||||
chr2:137992891
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.191-8027A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992891 | ||||||
chr2:137992967
|
G | GA | 6 | a0001c0001t0001g0089a0001c0001t0001g0213a0001c0001t0001g0214others(3): Show | 6 | HG01346.hp1 HG01952.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-7943dupA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137992967 | |||||
chr2:137992988
|
A | G | 1 | a0001c0001t0002g0273 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.191-7930A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992988 | ||||||
chr2:137993008
|
C | G | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191-7910C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993008 | ||||||
chr2:137993030
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.191-7888C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993030 | ||||||
chr2:137993367
|
G | C | 3 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG02109.hp1 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.191-7551G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993367 | ||||||
chr2:137993398
|
C | T | 1 | a0001c0001t0003g0028 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191-7520C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993398 | ||||||
chr2:137993448
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.191-7470A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993448 | ||||||
chr2:137993618
|
A | G | 1 | a0001c0001t0019g0195 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.191-7300A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993618 | ||||||
chr2:137993663
|
G | A | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-7255G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993663 | ||||||
chr2:137993832
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0143 | 2 | HG00621.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.191-7086C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993832 | ||||||
chr2:137994090
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-6828C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137994090 | ||||||
chr2:137994317
|
A | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG01243.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.191-6601A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137994317 | ||||||
chr2:137994319
|
G | A | 1 | a0003c0003t0001g0262 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.191-6599G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137994319 | ||||||
chr2:137994527
|
G | GT | 3 | a0001c0001t0006g0047a0001c0001t0006g0048a0001c0001t0006g0049 | 3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.191-6386dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137994527 | |||||
chr2:137994756
|
C | T | 1 | a0001c0001t0013g0145 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.191-6162C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137994756 | ||||||
chr2:137994760
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.191-6158A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137994760 | ||||||
chr2:137994964
|
C | T | 2 | a0001c0001t0003g0150a0001c0001t0003g0153 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.191-5954C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137994964 | ||||||
chr2:137995231
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.191-5687G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995231 | ||||||
chr2:137995249
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.191-5669T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995249 | ||||||
chr2:137995285
|
G | T | 1 | a0002c0002t0002g0234 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.191-5633G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995285 | ||||||
chr2:137995350
|
C | G | 1 | a0001c0001t0001g0239 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.191-5568C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995350 | ||||||
chr2:137995440
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.191-5478C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995440 | ||||||
chr2:137995556
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.191-5362G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995556 | ||||||
chr2:137995660
|
A | G | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-5258A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995660 | ||||||
chr2:137995753
|
A | G | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-5165A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995753 | ||||||
chr2:137996036
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.191-4882T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137996036 | ||||||
chr2:137996388
|
C | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 42 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.191-4530C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137996388 | ||||||
chr2:137996574
|
A | G | 2 | a0001c0001t0008g0182a0001c0001t0008g0184 | 2 | HG02698.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.191-4344A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137996574 | ||||||
chr2:137996734
|
G | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.191-4184G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137996734 | ||||||
chr2:137996804
|
G | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 44 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.191-4114G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137996804 | ||||||
chr2:137997374
|
A | C | 1 | a0001c0001t0002g0122 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.191-3544A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997374 | ||||||
chr2:137997380
|
C | A | 1 | a0001c0001t0001g0051 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.191-3538C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997380 | ||||||
chr2:137997434
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.191-3484G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997434 | ||||||
chr2:137997484
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.191-3434T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997484 | ||||||
chr2:137997633
|
G | T | 3 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0068 | 3 | HG02055.hp2 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.191-3285G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997633 | ||||||
chr2:137997689
|
A | C | 2 | a0001c0001t0001g0229a0001c0001t0001g0254 | 2 | HG01106.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.191-3229A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997689 | ||||||
chr2:137997859
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(132): Show | 165 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.191-3059T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997859 | ||||||
chr2:137997942
|
C | G | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.191-2976C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997942 | ||||||
chr2:137997989
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0209a0001c0001t0001g0228 | 3 | HG01261.hp2 HG01516.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.191-2929C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997989 | ||||||
chr2:137997990
|
G | A | 4 | a0001c0001t0004g0017a0001c0001t0004g0144a0001c0001t0004g0236others(1): Show | 5 | HG00735.hp1 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.191-2928G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997990 | ||||||
chr2:137998077
|
A | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0086a0001c0001t0002g0121others(2): Show | 8 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.191-2841A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998077 | ||||||
chr2:137998117
|
C | T | 1 | a0001c0001t0005g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.191-2801C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998117 | ||||||
chr2:137998164
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0218 | 2 | NA18975.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.191-2754T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998164 | ||||||
chr2:137998204
|
A | G | 1 | a0001c0001t0003g0038 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.191-2714A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998204 | ||||||
chr2:137998206
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.191-2712G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998206 | ||||||
chr2:137998227
|
G | A | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.191-2691G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998227 | ||||||
chr2:137998400
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.191-2518A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998400 | ||||||
chr2:137998422
|
T | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(135): Show | 168 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.191-2496T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998422 | ||||||
chr2:137998672
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.191-2246G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998672 | ||||||
chr2:137998875
|
A | G | 1 | a0001c0001t0002g0120 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.191-2043A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998875 | ||||||
chr2:137998988
|
C | CT | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.191-1923dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137998988 | |||||
chr2:137998996
|
C | A | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.191-1922C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998996 | ||||||
chr2:137999003
|
G | A | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-1915G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999003 | ||||||
chr2:137999075
|
T | C | 3 | a0001c0001t0006g0047a0001c0001t0006g0048a0001c0001t0006g0049 | 3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.191-1843T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999075 | ||||||
chr2:137999274
|
T | C | 3 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0068 | 3 | HG02055.hp2 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.191-1644T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999274 | ||||||
chr2:137999361
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.191-1557A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999361 | ||||||
chr2:137999430
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.191-1488C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999430 | ||||||
chr2:137999475
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.191-1443A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999475 | ||||||
chr2:137999506
|
G | T | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-1412G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999506 | ||||||
chr2:137999918
|
TA | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(263): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.191-988delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137999918 | |||||
chr2:138000021
|
T | C | 6 | a0001c0001t0002g0050a0001c0001t0002g0071a0001c0001t0002g0173others(3): Show | 6 | HG02572.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-897T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000021 | ||||||
chr2:138000095
|
C | G | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.191-823C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000095 | ||||||
chr2:138000148
|
T | C | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-770T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000148 | ||||||
chr2:138000169
|
G | A | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-749G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000169 | ||||||
chr2:138000184
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.191-734G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000184 | ||||||
chr2:138000277
|
C | A | 1 | a0002c0002t0002g0111 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.191-641C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000277 | ||||||
chr2:138000280
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.191-638C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000280 | ||||||
chr2:138000320
|
C | T | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-598C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000320 | ||||||
chr2:138000374
|
G | GT | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-544_191-543ins others(1): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000374 | ||||||
chr2:138000375
|
A | C | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-543A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000375 | ||||||
chr2:138000441
|
T | C | 9 | a0001c0001t0001g0089a0001c0001t0001g0180a0001c0001t0001g0213others(6): Show | 9 | HG00741.hp1 HG01255.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.191-477T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000441 | ||||||
chr2:138000455
|
A | T | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-463A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000455 | ||||||
chr2:138000467
|
A | AT | 111 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0194others(108): Show | 132 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.191-444dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 138000467 | |||||
chr2:138000528
|
T | C | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-390T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000528 | ||||||
chr2:138000567
|
TA | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.191-346delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 138000567 | |||||
chr2:138000568
|
A | T | 1 | a0001c0001t0002g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.191-350A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000568 | ||||||
chr2:138000583
|
T | A | 111 | a0001c0001t0001g0084a0001c0001t0001g0175a0001c0001t0001g0194others(108): Show | 132 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.191-335T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000583 | ||||||
chr2:138000630
|
T | A | 1 | a0001c0001t0004g0144 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.191-288T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000630 | ||||||
chr2:138000698
|
G | A | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-220G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000698 | ||||||
chr2:138000757
|
A | C | 1 | a0001c0001t0021g0265 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.191-161A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000757 | ||||||
chr2:138000789
|
G | T | 1 | a0001c0001t0001g0051 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.191-129G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000789 | ||||||
chr2:138001162
|
C | A | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+137C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001162 | ||||||
chr2:138001257
|
G | A | 1 | a0001c0001t0005g0032 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.298+232G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001257 | ||||||
chr2:138001275
|
A | C | 3 | a0001c0001t0003g0028a0001c0001t0010g0155a0001c0001t0010g0156 | 4 | HG02280.hp2 HG03209.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+250A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001275 | ||||||
chr2:138001385
|
A | G | 2 | a0001c0001t0010g0155a0001c0001t0010g0156 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.298+360A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001385 | ||||||
chr2:138001445
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.298+420G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001445 | ||||||
chr2:138001624
|
A | G | 4 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0068others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-440A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001624 | ||||||
chr2:138001693
|
T | C | 3 | a0001c0001t0003g0028a0001c0001t0010g0155a0001c0001t0010g0156 | 4 | HG02280.hp2 HG03209.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-371T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001693 | ||||||
chr2:138001751
|
T | TATC | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-312_299-310dup others(3): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 138001751 | |||||
chr2:138001851
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.299-213T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001851 | ||||||
chr2:138001900
|
C | A | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-164C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001900 | ||||||
chr2:138001921
|
C | T | 1 | a0001c0001t0013g0145 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299-143C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001921 | ||||||
chr2:138001951
|
C | T | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-113C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001951 | ||||||
chr2:138002242
|
AAT | A | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+58_429+59delTA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138002242 | |||||
chr2:138002243
|
A | G | 10 | a0001c0001t0002g0085a0001c0001t0002g0102a0001c0001t0002g0117others(7): Show | 10 | HG00438.hp1 HG00735.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+49A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002243 | ||||||
chr2:138002499
|
G | T | 2 | a0001c0001t0002g0006a0001c0001t0002g0120 | 5 | HG01943.hp2 HG02273.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+305G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002499 | ||||||
chr2:138002535
|
A | C | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+341A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002535 | ||||||
chr2:138002536
|
A | C | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+342A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002536 | ||||||
chr2:138002674
|
T | C | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+480T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002674 | ||||||
chr2:138002796
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.429+602A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002796 | ||||||
chr2:138002855
|
G | T | 2 | a0001c0001t0002g0081a0001c0001t0002g0116 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.429+661G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002855 | ||||||
chr2:138002939
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.429+745C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002939 | ||||||
chr2:138002980
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG02723.hp1 HG02818.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+786A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002980 | ||||||
chr2:138003044
|
T | C | 1 | a0002c0002t0002g0274 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.429+850T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003044 | ||||||
chr2:138003077
|
T | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.429+883T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003077 | ||||||
chr2:138003084
|
TGG | T | 80 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(77): Show | 99 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.429+893_429+894del others(2): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138003084 | |||||
chr2:138003087
|
G | T | 1 | a0001c0001t0002g0086 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.429+893G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003087 | ||||||
chr2:138003096
|
A | AG | 7 | a0001c0001t0001g0157a0001c0001t0002g0050a0001c0001t0002g0071others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+908dupG | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138003096 | |||||
chr2:138003113
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.429+919T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003113 | ||||||
chr2:138003114
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(267): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.429+920C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003114 | ||||||
chr2:138003147
|
G | A | 3 | a0001c0001t0003g0028a0001c0001t0010g0155a0001c0001t0010g0156 | 4 | HG02280.hp2 HG03209.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+953G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003147 | ||||||
chr2:138003158
|
G | A | 3 | a0001c0001t0006g0047a0001c0001t0006g0048a0001c0001t0006g0049 | 3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.429+964G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003158 | ||||||
chr2:138003199
|
C | T | 80 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(77): Show | 99 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.429+1005C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003199 | ||||||
chr2:138003240
|
T | TA | 20 | a0001c0001t0001g0194a0001c0001t0002g0050a0001c0001t0002g0071others(17): Show | 20 | HG00609.hp2 HG02109.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.429+1048dupA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138003240 | |||||
chr2:138003243
|
T | A | 20 | a0001c0001t0001g0194a0001c0001t0002g0050a0001c0001t0002g0071others(17): Show | 20 | HG00609.hp2 HG02109.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.429+1049T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003243 | ||||||
chr2:138003243
|
T | TA | 3 | a0001c0001t0003g0028a0001c0001t0010g0155a0001c0001t0010g0156 | 4 | HG02280.hp2 HG03209.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+1051dupA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138003243 | |||||
chr2:138003246
|
T | A | 113 | a0001c0001t0001g0194a0001c0001t0002g0004a0001c0001t0002g0005others(110): Show | 133 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.429+1052T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003246 | ||||||
chr2:138003275
|
T | C | 2 | a0001c0001t0005g0032a0001c0001t0005g0033 | 3 | HG02258.hp2 HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.429+1081T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003275 | ||||||
chr2:138003433
|
A | G | 106 | a0001c0001t0001g0175a0001c0001t0001g0194a0001c0001t0002g0004others(103): Show | 127 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.429+1239A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003433 | ||||||
chr2:138003483
|
A | G | 2 | a0001c0001t0003g0076a0001c0001t0013g0145 | 2 | HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.429+1289A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003483 | ||||||
chr2:138003525
|
C | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG01243.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+1331C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003525 | ||||||
chr2:138003571
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.429+1377A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003571 | ||||||
chr2:138003597
|
T | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.429+1403T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003597 | ||||||
chr2:138003653
|
A | G | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+1459A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003653 | ||||||
chr2:138003679
|
C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0185others(2): Show | 7 | HG02056.hp1 HG02080.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-1453C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003679 | ||||||
chr2:138003689
|
C | A | 4 | a0001c0001t0004g0017a0001c0001t0004g0144a0001c0001t0004g0236others(1): Show | 5 | HG00735.hp1 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-1443C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003689 | ||||||
chr2:138003729
|
G | A | 21 | a0001c0001t0003g0028a0001c0001t0003g0034a0001c0001t0003g0037others(18): Show | 23 | HG00735.hp1 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.430-1403G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003729 | ||||||
chr2:138003770
|
C | G | 3 | a0001c0001t0006g0047a0001c0001t0006g0048a0001c0001t0006g0049 | 3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.430-1362C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003770 | ||||||
chr2:138003995
|
C | T | 102 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(99): Show | 122 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.430-1137C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003995 | ||||||
chr2:138004107
|
T | G | 1 | a0001c0001t0001g0093 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.430-1025T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004107 | ||||||
chr2:138004134
|
T | TA | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(146): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.430-997dupA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138004134 | |||||
chr2:138004180
|
G | C | 1 | a0001c0001t0003g0038 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.430-952G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004180 | ||||||
chr2:138004365
|
GGACAGGC others(13): Show |
G | 1 | a0001c0001t0001g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.430-764_430-745del others(20): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138004365 | |||||
chr2:138004442
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.430-690G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004442 | ||||||
chr2:138004486
|
C | A | 116 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 138 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.430-646C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004486 | ||||||
chr2:138004486
|
C | G | 2 | a0001c0001t0003g0061a0001c0001t0003g0062 | 2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.430-646C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004486 | ||||||
chr2:138004567
|
A | T | 1 | a0001c0001t0001g0175 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.430-565A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004567 | ||||||
chr2:138004598
|
C | A | 87 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(84): Show | 105 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.430-534C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004598 | ||||||
chr2:138004812
|
C | T | 1 | a0001c0001t0002g0015 | 2 | NA18961.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.430-320C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004812 | ||||||
chr2:138004875
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.430-257A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004875 | ||||||
chr2:138004990
|
C | T | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-142C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004990 | ||||||
chr2:138005273
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.523+48G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005273 | ||||||
chr2:138005281
|
G | A | 23 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0067others(20): Show | 25 | HG00735.hp1 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.523+56G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005281 | ||||||
chr2:138005303
|
C | CTT | 81 | a0001c0001t0001g0084a0001c0001t0002g0004a0001c0001t0002g0005others(78): Show | 100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.523+79_523+80dupTT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138005303 | |||||
chr2:138005460
|
T | C | 95 | a0001c0001t0001g0084a0001c0001t0002g0004a0001c0001t0002g0005others(92): Show | 114 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.523+235T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005460 | ||||||
chr2:138005571
|
G | T | 5 | a0001c0001t0002g0050a0001c0001t0002g0071a0001c0001t0002g0173others(2): Show | 5 | HG02572.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+346G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005571 | ||||||
chr2:138005597
|
T | G | 3 | a0001c0001t0001g0220a0001c0001t0001g0242a0001c0001t0001g0253 | 3 | HG03710.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.523+372T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005597 | ||||||
chr2:138005717
|
C | A | 94 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(91): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+492C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005717 | ||||||
chr2:138005760
|
A | G | 23 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0067others(20): Show | 25 | HG00735.hp1 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.523+535A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005760 | ||||||
chr2:138005850
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.523+625G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005850 | ||||||
chr2:138005927
|
GAT | G | 94 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(91): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+704_523+705del others(2): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138005927 | |||||
chr2:138005943
|
T | A | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+718T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005943 | ||||||
chr2:138005976
|
T | G | 94 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(91): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+751T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005976 | ||||||
chr2:138005983
|
G | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.523+758G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005983 | ||||||
chr2:138006040
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.523+815C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006040 | ||||||
chr2:138006116
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0183 | 2 | HG02071.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.523+891C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006116 | ||||||
chr2:138006191
|
C | G | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.523+966C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006191 | ||||||
chr2:138006245
|
C | T | 80 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(77): Show | 99 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.523+1020C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006245 | ||||||
chr2:138006328
|
T | G | 94 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(91): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+1103T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006328 | ||||||
chr2:138006364
|
G | A | 94 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(91): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+1139G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006364 | ||||||
chr2:138006430
|
G | A | 3 | a0001c0001t0006g0047a0001c0001t0006g0048a0001c0001t0006g0049 | 3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.523+1205G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006430 | ||||||
chr2:138006575
|
C | G | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.523+1350C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006575 | ||||||
chr2:138006692
|
A | G | 1 | a0001c0001t0005g0032 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.523+1467A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006692 | ||||||
chr2:138006744
|
A | G | 94 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(91): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+1519A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006744 | ||||||
chr2:138006759
|
T | A | 3 | a0001c0001t0008g0182a0001c0001t0008g0184a0001c0001t0008g0210 | 3 | HG02165.hp1 HG02698.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.523+1534T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006759 | ||||||
chr2:138006808
|
C | T | 12 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0067others(9): Show | 13 | HG00735.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.523+1583C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006808 | ||||||
chr2:138006830
|
T | C | 4 | a0002c0002t0002g0030a0002c0002t0002g0267a0002c0002t0002g0271others(1): Show | 5 | HG01346.hp2 HG01928.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+1605T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006830 | ||||||
chr2:138006839
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG02109.hp1 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.523+1614C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006839 | ||||||
chr2:138006871
|
TA | T | 94 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(91): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+1654delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138006871 | |||||
chr2:138006891
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.523+1666G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006891 | ||||||
chr2:138006901
|
C | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0226a0001c0001t0001g0239others(1): Show | 8 | NA18941.hp1 NA18949.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.523+1676C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006901 | ||||||
chr2:138007205
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.523+1980G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007205 | ||||||
chr2:138007235
|
A | G | 1 | a0001c0001t0017g0225 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.523+2010A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007235 | ||||||
chr2:138007250
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0185a0001c0001t0001g0227 | 4 | NA18989.hp1 NA19001.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.523+2025C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007250 | ||||||
chr2:138007340
|
A | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0253 | 2 | HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.523+2115A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007340 | ||||||
chr2:138007349
|
T | A | 118 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 140 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.523+2124T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007349 | ||||||
chr2:138007481
|
A | G | 118 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 140 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.523+2256A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007481 | ||||||
chr2:138007491
|
C | T | 2 | a0001c0001t0003g0061a0001c0001t0003g0062 | 2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.523+2266C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007491 | ||||||
chr2:138007513
|
G | C | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.523+2288G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007513 | ||||||
chr2:138007516
|
C | T | 8 | a0001c0001t0002g0085a0001c0001t0002g0102a0001c0001t0002g0118others(5): Show | 8 | HG00438.hp1 HG02071.hp2 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.523+2291C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007516 | ||||||
chr2:138007637
|
A | G | 2 | a0001c0001t0005g0032a0001c0001t0005g0033 | 3 | HG02258.hp2 HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.523+2412A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007637 | ||||||
chr2:138007698
|
G | A | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+2473G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007698 | ||||||
chr2:138007875
|
G | C | 1 | a0001c0001t0001g0213 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.523+2650G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007875 | ||||||
chr2:138008092
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.523+2867T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008092 | ||||||
chr2:138008173
|
C | T | 94 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(91): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+2948C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008173 | ||||||
chr2:138008190
|
T | C | 6 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(3): Show | 6 | HG02145.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.523+2965T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008190 | ||||||
chr2:138008225
|
T | G | 1 | a0001c0001t0001g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.523+3000T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008225 | ||||||
chr2:138008301
|
C | T | 5 | a0001c0001t0002g0050a0001c0001t0002g0071a0001c0001t0002g0173others(2): Show | 5 | HG02572.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+3076C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008301 | ||||||
chr2:138008360
|
G | A | 1 | a0001c0001t0002g0102 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.523+3135G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008360 | ||||||
chr2:138008364
|
C | T | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.523+3139C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008364 | ||||||
chr2:138008414
|
T | C | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.523+3189T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008414 | ||||||
chr2:138008439
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.523+3214G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008439 | ||||||
chr2:138008523
|
C | T | 94 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(91): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+3298C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008523 | ||||||
chr2:138008534
|
G | A | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.523+3309G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008534 | ||||||
chr2:138008607
|
C | T | 6 | a0001c0001t0004g0017a0001c0001t0004g0144a0001c0001t0004g0236others(3): Show | 7 | HG00735.hp1 HG02809.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.523+3382C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008607 | ||||||
chr2:138008625
|
A | G | 1 | a0001c0001t0003g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.523+3400A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008625 | ||||||
chr2:138008630
|
C | T | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.523+3405C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008630 | ||||||
chr2:138008693
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.523+3468T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008693 | ||||||
chr2:138008708
|
T | C | 1 | a0001c0001t0003g0028 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.523+3483T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008708 | ||||||
chr2:138008712
|
T | G | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.523+3487T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008712 | ||||||
chr2:138008906
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.523+3681G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008906 | ||||||
chr2:138009137
|
A | G | 3 | a0001c0001t0006g0047a0001c0001t0006g0048a0001c0001t0006g0049 | 3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.523+3912A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009137 | ||||||
chr2:138009270
|
G | C | 23 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0067others(20): Show | 25 | HG00735.hp1 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.523+4045G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009270 | ||||||
chr2:138009387
|
C | T | 94 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(91): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+4162C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009387 | ||||||
chr2:138009430
|
C | A | 2 | a0001c0001t0005g0032a0001c0001t0005g0033 | 3 | HG02258.hp2 HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.523+4205C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009430 | ||||||
chr2:138009515
|
A | G | 1 | a0001c0001t0005g0032 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.524-4260A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009515 | ||||||
chr2:138009685
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG00408.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.524-4090T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009685 | ||||||
chr2:138009729
|
C | G | 83 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(80): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.524-4046C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009729 | ||||||
chr2:138009742
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.524-4033T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009742 | ||||||
chr2:138009931
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.524-3844T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009931 | ||||||
chr2:138009957
|
T | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(146): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.524-3818T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009957 | ||||||
chr2:138010016
|
A | G | 1 | a0001c0001t0019g0195 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.524-3759A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010016 | ||||||
chr2:138010181
|
T | C | 1 | a0001c0001t0002g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.524-3594T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010181 | ||||||
chr2:138010240
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.524-3535T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010240 | ||||||
chr2:138010318
|
C | CA | 94 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(91): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.524-3450dupA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010318 | |||||
chr2:138010434
|
G | GAC | 4 | a0001c0001t0002g0069a0001c0001t0019g0195a0002c0002t0002g0138others(1): Show | 4 | HG01361.hp2 HG01516.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-3336_524-3335d others(4): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010434 | |||||
chr2:138010434
|
G | GACAC | 3 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0002g0122 | 6 | HG00408.hp1 HG00597.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.524-3338_524-3335d others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010434 | |||||
chr2:138010434
|
G | GACACACA others(3): Show |
2 | a0001c0001t0002g0112a0001c0001t0002g0137 | 2 | NA18968.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.524-3335_524-3334i others(12): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010434 | |||||
chr2:138010434
|
GACACACG others(5): Show |
G | 1 | a0001c0001t0002g0085 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.524-3334_524-3323d others(14): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010434 | |||||
chr2:138010435
|
A | ACACACAC others(1): Show |
9 | a0001c0001t0002g0081a0001c0001t0002g0113a0001c0001t0002g0116others(6): Show | 9 | HG00438.hp1 HG02071.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.524-3335_524-3334i others(10): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010435 | |||||
chr2:138010437
|
A | ACACACG | 18 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0015others(15): Show | 24 | HG00423.hp2 HG00639.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.524-3335_524-3334i others(8): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010437 | |||||
chr2:138010437
|
ACACG | A | 5 | a0001c0001t0002g0050a0001c0001t0002g0071a0001c0001t0002g0173others(2): Show | 5 | HG02572.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.524-3334_524-3331d others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010437 | |||||
chr2:138010439
|
A | ACACG | 34 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0014others(31): Show | 43 | HG00280.hp1 HG00558.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.524-3335_524-3334i others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010439 | |||||
chr2:138010439
|
ACG | A | 5 | a0001c0001t0002g0073a0001c0001t0002g0123a0001c0001t0008g0182others(2): Show | 5 | HG01261.hp1 HG02165.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.524-3334_524-3333d others(4): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010439 | |||||
chr2:138010441
|
G | A | 73 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(70): Show | 92 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.524-3334G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010441 | ||||||
chr2:138010441
|
G | GCA | 30 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(27): Show | 34 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.524-3293_524-3292d others(4): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | |||||
chr2:138010441
|
G | GCACA | 11 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0064others(8): Show | 11 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.524-3295_524-3292d others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | |||||
chr2:138010441
|
G | GCACACA | 7 | a0001c0001t0001g0026a0001c0001t0001g0179a0001c0001t0001g0191others(4): Show | 8 | HG02056.hp1 HG02080.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.524-3297_524-3292d others(8): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | |||||
chr2:138010441
|
GCA | G | 5 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0165others(2): Show | 6 | HG01243.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.524-3293_524-3292d others(4): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | |||||
chr2:138010441
|
GCACA | G | 3 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0003g0041 | 3 | HG02647.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.524-3295_524-3292d others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | |||||
chr2:138010441
|
GCACACA | G | 9 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.524-3297_524-3292d others(8): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | |||||
chr2:138010441
|
GCACACAC others(1): Show |
G | 4 | a0001c0001t0003g0028a0001c0001t0003g0067a0001c0001t0003g0070others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.524-3299_524-3292d others(10): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | |||||
chr2:138010441
|
GCACACAC others(3): Show |
G | 6 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0068others(3): Show | 6 | HG00735.hp1 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.524-3301_524-3292d others(12): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | |||||
chr2:138010441
|
GCACACAC others(5): Show |
G | 3 | a0001c0001t0004g0017a0001c0001t0004g0144a0001c0001t0004g0236 | 4 | HG02809.hp1 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-3303_524-3292d others(14): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | |||||
chr2:138010441
|
GCACACAC others(7): Show |
G | 1 | a0001c0001t0010g0155 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.524-3305_524-3292d others(16): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | |||||
chr2:138010443
|
A | G | 5 | a0001c0001t0002g0018a0001c0001t0002g0152a0001c0001t0002g0154others(2): Show | 6 | HG02300.hp1 HG02615.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-3332A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010443 | ||||||
chr2:138010445
|
A | G | 5 | a0001c0001t0002g0073a0001c0001t0002g0123a0001c0001t0008g0182others(2): Show | 5 | HG01261.hp1 HG02165.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.524-3330A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010445 | ||||||
chr2:138010447
|
A | G | 6 | a0001c0001t0002g0050a0001c0001t0002g0071a0001c0001t0002g0173others(3): Show | 6 | HG02572.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-3328A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010447 | ||||||
chr2:138010449
|
A | G | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-3326A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010449 | ||||||
chr2:138010451
|
A | G | 5 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.524-3324A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010451 | ||||||
chr2:138010455
|
A | G | 1 | a0001c0001t0002g0085 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.524-3320A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010455 | ||||||
chr2:138010474
|
CACACACA others(3): Show |
C | 1 | a0001c0001t0001g0022 | 2 | NA18979.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.524-3300_524-3291d others(12): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010474 | ||||||
chr2:138010478
|
CACACAG | C | 4 | a0001c0001t0001g0161a0001c0001t0001g0242a0001c0001t0007g0077others(1): Show | 4 | HG02258.hp1 HG03710.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-3296_524-3291d others(8): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010478 | ||||||
chr2:138010480
|
CACAG | C | 11 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0146others(8): Show | 12 | HG00639.hp2 HG01168.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.524-3294_524-3291d others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010480 | ||||||
chr2:138010482
|
CAG | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0013others(44): Show | 56 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.524-3292_524-3291d others(4): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010482 | ||||||
chr2:138010484
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0250 | 2 | HG03225.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.524-3291G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010484 | ||||||
chr2:138010484
|
G | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(75): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.524-3291G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010484 | ||||||
chr2:138010529
|
A | C | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-3246A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010529 | ||||||
chr2:138010766
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.524-3009G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010766 | ||||||
chr2:138010768
|
T | C | 1 | a0001c0001t0002g0008 | 3 | HG02630.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.524-3007T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010768 | ||||||
chr2:138010925
|
A | C | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-2850A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010925 | ||||||
chr2:138011035
|
C | T | 118 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 140 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.524-2740C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011035 | ||||||
chr2:138011348
|
C | A | 1 | a0001c0001t0003g0067 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.524-2427C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011348 | ||||||
chr2:138011422
|
G | C | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-2353G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011422 | ||||||
chr2:138011530
|
T | A | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-2245T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011530 | ||||||
chr2:138011566
|
A | G | 6 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0038others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-2209A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011566 | ||||||
chr2:138011949
|
G | A | 13 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0067others(10): Show | 14 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.524-1826G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011949 | ||||||
chr2:138011953
|
T | C | 3 | a0001c0001t0002g0069a0001c0001t0002g0088a0001c0001t0002g0149 | 3 | HG00639.hp1 HG00741.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.524-1822T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011953 | ||||||
chr2:138012055
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.524-1720A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012055 | ||||||
chr2:138012099
|
C | T | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-1676C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012099 | ||||||
chr2:138012293
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.524-1482G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012293 | ||||||
chr2:138012337
|
G | C | 1 | a0001c0001t0015g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.524-1438G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012337 | ||||||
chr2:138012381
|
T | C | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-1394T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012381 | ||||||
chr2:138012397
|
G | A | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-1378G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012397 | ||||||
chr2:138012575
|
T | C | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-1200T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012575 | ||||||
chr2:138012579
|
G | C | 4 | a0001c0001t0003g0070a0001c0001t0003g0072a0001c0001t0003g0150others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.524-1196G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012579 | ||||||
chr2:138012695
|
C | A | 48 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(45): Show | 61 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.524-1080C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012695 | ||||||
chr2:138012741
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.524-1034G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012741 | ||||||
chr2:138012755
|
T | C | 1 | a0001c0001t0003g0028 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.524-1020T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012755 | ||||||
chr2:138012791
|
A | G | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-984A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012791 | ||||||
chr2:138012792
|
T | A | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-983T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012792 | ||||||
chr2:138012793
|
C | A | 1 | a0001c0001t0002g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.524-982C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012793 | ||||||
chr2:138012812
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.524-963C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012812 | ||||||
chr2:138012935
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.524-840G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012935 | ||||||
chr2:138013285
|
C | T | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-490C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138013285 | ||||||
chr2:138013481
|
C | G | 1 | a0001c0001t0005g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.524-294C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138013481 | ||||||
chr2:138013482
|
A | G | 100 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(97): Show | 120 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.524-293A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138013482 | ||||||
chr2:138013600
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.524-175A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138013600 | ||||||
chr2:138013649
|
G | A | 88 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(85): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-126G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138013649 | ||||||
chr2:138013753
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0218 | 2 | NA18975.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.524-22T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138013753 |