Item | Value |
---|---|
geneid | 135114 |
ensemblid | ENSG00000111911.7 |
hgncid | 18468 |
symbol | HINT3 |
name | histidine triad nucleotide binding protein 3 |
refseq_nuc | NM_138571.5 |
refseq_prot | NP_612638.3 |
ensembl_nuc | ENST00000229633.7 |
ensembl_prot | ENSP00000229633.5 |
mane_status | MANE Select |
chr | chr6 |
start | 125956770 |
end | 125980244 |
strand | + |
ver | v1.2 |
region | chr6:125956770-125980244 |
region5000 | chr6:125951770-125985244 |
regionname0 | HINT3_chr6_125956770_125980244 |
regionname5000 | HINT3_chr6_125951770_125985244 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 182 | 166 | 58 | 27 | 57 | 9 | 14 | 36 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0002 | 1/0 | 182 | 101 | 33 | 29 | 11 | 9 | 18 | 8 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0003 | 0/0 | 182 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 549 | 165 | 57 | 27 | 57 | 9 | 14 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 | |
c0002 | 1/0 | 549 | 100 | 33 | 29 | 11 | 9 | 17 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 | |
c0003 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 | |
c0004 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 | |
c0005 | 0/0 | 549 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2779 | 152 | 33 | 31 | 56 | 12 | 19 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0002 | 1/0 | 2777 | 67 | 22 | 17 | 11 | 5 | 11 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0003 | 0/0 | 2779 | 18 | 18 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0004 | 0/0 | 2779 | 10 | 9 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0005 | 0/0 | 2779 | 3 | 3 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0006 | 0/0 | 2777 | 2 | 0 | 1 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0007 | 0/0 | 2777 | 2 | 0 | 0 | 0 | 0 | 2 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0008 | 0/0 | 2779 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0009 | 0/0 | 2777 | 2 | 1 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0010 | 0/0 | 2779 | 2 | 0 | 2 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0011 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0012 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0013 | 0/0 | 2779 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0014 | 0/0 | 2779 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0015 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0016 | 0/0 | 2779 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0017 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
t0018 | 0/0 | 2779 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 3 | 2 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0002 | 0/0 | 5 | 0 | 1 | 0 | 0 | 4 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0004 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0008 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0011 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 549 | 165 | 57 | 27 | 57 | 9 | 14 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 | |
a0001c0004 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 | |
a0002c0002 | 1/0 | 549 | 100 | 33 | 29 | 11 | 9 | 17 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 | |
a0002c0005 | 0/0 | 549 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 | |
a0003c0003 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3327 | 131 | 28 | 23 | 56 | 9 | 14 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0001c0001t0003 | 0/0 | 3327 | 17 | 17 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0001c0001t0004 | 0/0 | 3327 | 5 | 5 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0001c0001t0005 | 0/0 | 3327 | 3 | 3 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0001c0001t0008 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0001c0001t0010 | 0/0 | 3327 | 2 | 0 | 2 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0001c0001t0011 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0001c0001t0012 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0001c0001t0014 | 0/0 | 3327 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0001c0001t0016 | 0/0 | 3327 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0001c0001t0018 | 0/0 | 3327 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0001c0004t0001 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0002c0002t0001 | 0/0 | 3327 | 20 | 4 | 8 | 0 | 3 | 5 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0002c0002t0002 | 1/0 | 3325 | 66 | 22 | 17 | 11 | 5 | 10 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0002c0002t0004 | 0/0 | 3327 | 5 | 4 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0002c0002t0006 | 0/0 | 3325 | 2 | 0 | 1 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0002c0002t0007 | 0/0 | 3325 | 2 | 0 | 0 | 0 | 0 | 2 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0002c0002t0009 | 0/0 | 3325 | 2 | 1 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0002c0002t0013 | 0/0 | 3327 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0002c0002t0015 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0002c0002t0017 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0002c0005t0002 | 0/0 | 3325 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
a0003c0003t0003 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | copy fasta | chr6 | 125951770 | 125985244 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 3 | 1 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0010g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0010g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0012g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0014g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0001t0018g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0001c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0002 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0011 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0006g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0007g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0009g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0013g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0015g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0002t0017g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0002c0005t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
a0003c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | GBR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0079 | EUR | GBR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0011 | EUR | GBR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0030 | EUR | FIN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0086 | EUR | FIN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0060 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00642 | hp2 | a0002 | c0002 | t0009 | g0052 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0047 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0077 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0085 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01109 | hp2 | a0002 | c0002 | t0006 | g0012 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0016 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01192 | hp1 | a0002 | c0002 | t0004 | g0209 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0073 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01243 | hp1 | a0001 | c0001 | t0018 | g0031 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01256 | hp1 | a0001 | c0001 | t0010 | g0003 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0059 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01258 | hp2 | a0001 | c0001 | t0010 | g0023 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01358 | hp2 | a0002 | c0002 | t0013 | g0219 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0015 | EUR | IBS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01516 | hp1 | a0002 | c0002 | t0006 | g0012 | EUR | IBS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0015 | EUR | IBS | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01943 | hp1 | a0001 | c0001 | t0014 | g0032 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0041 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0054 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02055 | hp2 | a0002 | c0002 | t0004 | g0210 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | CDX | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0082 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0193 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0043 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02451 | hp2 | a0002 | c0002 | t0015 | g0081 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02572 | hp1 | a0002 | c0002 | t0009 | g0056 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02572 | hp2 | a0002 | c0002 | t0002 | g0044 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0216 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02615 | hp2 | a0002 | c0002 | t0004 | g0027 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02622 | hp2 | a0002 | c0002 | t0002 | g0057 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02647 | hp1 | a0002 | c0002 | t0002 | g0071 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02683 | hp2 | a0002 | c0005 | t0002 | g0002 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02698 | hp1 | a0002 | c0002 | t0007 | g0029 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0066 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02723 | hp1 | a0002 | c0002 | t0017 | g0206 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02818 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0093 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02896 | hp1 | a0002 | c0002 | t0002 | g0069 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0080 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02976 | hp1 | a0002 | c0002 | t0004 | g0027 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0087 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03041 | hp1 | a0002 | c0002 | t0002 | g0070 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0055 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03225 | hp2 | a0001 | c0001 | t0011 | g0194 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0222 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0048 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0040 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0089 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | ESN | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03540 | hp2 | a0003 | c0003 | t0003 | g0028 | AFR | GWD | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0118 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0078 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03669 | hp2 | a0002 | c0002 | t0007 | g0029 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0053 | SAS | PJL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0049 | SAS | BEB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0072 | SAS | STU | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | YRI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | YRI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19003 | hp2 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | LWK | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | LWK | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0042 | AFR | YRI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0214 | AFR | YRI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0074 | AFR | ASW | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ASW | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0128 | EUR | TSI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0004 | EUR | TSI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | GIH | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | GIH | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0076 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02486 | hp1 | a0002 | c0002 | t0004 | g0204 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0051 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0212 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03471 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | USA | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | USA | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0215 | AFR | USA | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | USA | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0218 | AFR | LWK | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | LWK | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0144 | REF | REF | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0011 | REF | REF | HINT3_chr6_125951770_125985244 | HINT3 | chr6 | 125951770 | 125985244 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:125957084 | G | C | 2 | a0001a0003 | 167 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(164): Show |
missense_variant | MODERATE | c.107G>C | p.Gly36Ala | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/5 | 315/3325 | 107/549 | 36/182 | chr6 | 125957084 | ||
chr6:125966963 | T | C | 1 | a0003 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.278T>C | p.Ile93Thr | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/5 | 486/3325 | 278/549 | 93/182 | chr6 | 125966963 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:125957130 | C | T | 1 | a0002c0005 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.153C>T | p.Cys51Cys | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/5 | 361/3325 | 153/549 | 51/182 | chr6 | 125957130 | ||
chr6:125974940 | G | A | 1 | a0001c0004 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.483G>A | p.Leu161Leu | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/5 | 691/3325 | 483/549 | 161/182 | chr6 | 125974940 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:125956834 | C | T | 1 | a0001c0001t0018 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-144C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/5 | 144 | chr6 | 125956834 | |||||
chr6:125956930 | C | T | 1 | a0001c0001t0010 | 2 | HG01256.hp1 HG01258.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-48C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/5 | chr6 | 125956930 | ||||||
chr6:125977980 | A | T | 1 | a0001c0001t0018 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*304A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 304 | chr6 | 125977980 | |||||
chr6:125978071 | A | T | 1 | a0002c0002t0009 | 2 | HG00642.hp2 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*395A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 395 | chr6 | 125978071 | |||||
chr6:125978118 | A | T | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*442A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 442 | chr6 | 125978118 | |||||
chr6:125978159 | A | G | 1 | a0002c0002t0017 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*483A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 483 | chr6 | 125978159 | |||||
chr6:125978297 | A | T | 3 | a0001c0001t0004a0002c0002t0004a0002c0002t0017 | 11 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*621A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 621 | chr6 | 125978297 | |||||
chr6:125978562 | C | T | 1 | a0001c0001t0016 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*886C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 886 | chr6 | 125978562 | |||||
chr6:125978624 | T | C | 1 | a0001c0001t0011 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*948T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 948 | chr6 | 125978624 | |||||
chr6:125978641 | C | A | 1 | a0001c0001t0012 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*965C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 965 | chr6 | 125978641 | |||||
chr6:125978773 | A | G | 1 | a0001c0001t0008 | 2 | HG02976.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1097A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1097 | chr6 | 125978773 | |||||
chr6:125978838 | A | ACT | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*1162_*1163insCT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1163 | chr6 | 125978838 | |||||
chr6:125979000 | G | A | 1 | a0002c0002t0013 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1324G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1324 | chr6 | 125979000 | |||||
chr6:125979124 | G | A | 16 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(13): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*1448G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1448 | chr6 | 125979124 | |||||
chr6:125979184 | T | C | 1 | a0001c0001t0018 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1508T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1508 | chr6 | 125979184 | |||||
chr6:125979272 | G | T | 2 | a0001c0001t0008a0001c0001t0012 | 3 | HG02976.hp2 HG03453.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1596G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1596 | chr6 | 125979272 | |||||
chr6:125979299 | A | G | 6 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(3): Show | 32 | HG01192.hp1 HG01891.hp2 HG02055.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1623A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1623 | chr6 | 125979299 | |||||
chr6:125979431 | G | A | 1 | a0002c0002t0006 | 2 | HG01109.hp2 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1755G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 1755 | chr6 | 125979431 | |||||
chr6:125979709 | G | A | 1 | a0001c0001t0005 | 3 | HG02895.hp1 HG03579.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2033G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 2033 | chr6 | 125979709 | |||||
chr6:125979821 | A | G | 17 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(14): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*2145A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 2145 | chr6 | 125979821 | |||||
chr6:125979907 | G | A | 1 | a0001c0001t0014 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2231G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 2231 | chr6 | 125979907 | |||||
chr6:125980139 | C | T | 1 | a0002c0002t0015 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2463C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 2463 | chr6 | 125980139 | |||||
chr6:125980219 | A | G | 1 | a0002c0002t0007 | 2 | HG02698.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2543A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 5/5 | 2543 | chr6 | 125980219 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:125957443 | C | A | 1 | a0001c0001t0018g0031 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.201+265C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125957443 | ||||||
chr6:125957481 | C | T | 1 | a0002c0002t0002g0223 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.201+303C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125957481 | ||||||
chr6:125957908 | T | A | 1 | a0001c0001t0014g0032 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.201+730T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125957908 | ||||||
chr6:125957909 | A | T | 6 | a0002c0002t0001g0030a0002c0002t0001g0218a0002c0002t0001g0220others(3): Show | 7 | HG00280.hp2 HG00642.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+731A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125957909 | ||||||
chr6:125957912 | A | C | 1 | a0001c0001t0004g0217 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.201+734A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125957912 | ||||||
chr6:125958041 | C | T | 2 | a0002c0002t0002g0216a0002c0002t0007g0029 | 3 | HG02602.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.201+863C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958041 | ||||||
chr6:125958042 | G | T | 21 | a0001c0001t0003g0028a0001c0001t0003g0200a0001c0001t0003g0201others(18): Show | 22 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.201+864G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958042 | ||||||
chr6:125958120 | AG | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG02809.hp2 HG02970.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+944delG | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125958120 | |||||
chr6:125958280 | G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.201+1102G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958280 | ||||||
chr6:125958428 | T | C | 1 | a0001c0001t0018g0031 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.201+1250T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958428 | ||||||
chr6:125958505 | A | C | 4 | a0001c0001t0003g0195a0001c0001t0003g0196a0001c0001t0003g0197others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+1327A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958505 | ||||||
chr6:125958881 | G | A | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.201+1703G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958881 | ||||||
chr6:125958901 | C | A | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.201+1723C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125958901 | ||||||
chr6:125959188 | C | T | 1 | a0001c0001t0011g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.201+2010C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125959188 | ||||||
chr6:125959369 | C | T | 2 | a0001c0001t0001g0192a0001c0004t0001g0193 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.201+2191C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125959369 | ||||||
chr6:125959373 | A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(155): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.201+2195A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125959373 | ||||||
chr6:125959486 | G | A | 45 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0090others(42): Show | 47 | HG00741.hp1 HG01192.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.201+2308G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125959486 | ||||||
chr6:125959880 | C | T | 2 | a0001c0001t0001g0192a0001c0004t0001g0193 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.201+2702C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125959880 | ||||||
chr6:125960093 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.201+2915T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960093 | ||||||
chr6:125960113 | C | T | 21 | a0001c0001t0003g0028a0001c0001t0003g0200a0001c0001t0003g0201others(18): Show | 22 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.201+2935C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960113 | ||||||
chr6:125960320 | G | T | 1 | a0001c0001t0001g0191 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.201+3142G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960320 | ||||||
chr6:125960371 | T | C | 1 | a0001c0001t0008g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.201+3193T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960371 | ||||||
chr6:125960396 | C | T | 40 | a0001c0001t0001g0018a0001c0001t0001g0090a0001c0001t0001g0096others(37): Show | 42 | HG00741.hp1 HG01192.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.201+3218C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960396 | ||||||
chr6:125960451 | G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0103 | 4 | HG00408.hp1 HG02083.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+3273G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960451 | ||||||
chr6:125960613 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.201+3435C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960613 | ||||||
chr6:125960616 | C | T | 1 | a0002c0002t0002g0086 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.201+3438C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960616 | ||||||
chr6:125960655 | T | TG | 22 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0103others(19): Show | 23 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.201+3487dupG | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125960655 | |||||
chr6:125960657 | G | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0090 | 3 | HG02896.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.201+3479G>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960657 | ||||||
chr6:125960665 | GA | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0033others(29): Show | 37 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.201+3496delA | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125960665 | |||||
chr6:125960666 | A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(109): Show | 129 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.201+3488A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960666 | ||||||
chr6:125960667 | A | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0107 | 4 | HG02040.hp1 HG02040.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+3489A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960667 | ||||||
chr6:125960667 | A | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0019others(123): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.201+3489A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960667 | ||||||
chr6:125960668 | A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(130): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.201+3490A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960668 | ||||||
chr6:125960669 | A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(127): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.201+3491A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960669 | ||||||
chr6:125960670 | A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(127): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.201+3492A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960670 | ||||||
chr6:125960671 | A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(127): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.201+3493A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960671 | ||||||
chr6:125960672 | A | G | 11 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0034others(8): Show | 12 | HG00280.hp1 HG01106.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.201+3494A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960672 | ||||||
chr6:125960718 | A | T | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.201+3540A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960718 | ||||||
chr6:125960929 | T | C | 1 | a0001c0001t0011g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.201+3751T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960929 | ||||||
chr6:125960997 | A | T | 1 | a0001c0004t0001g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.201+3819A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125960997 | ||||||
chr6:125961062 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.201+3884A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961062 | ||||||
chr6:125961111 | A | G | 1 | a0001c0001t0003g0211 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.201+3933A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961111 | ||||||
chr6:125961140 | G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(127): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.201+3962G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961140 | ||||||
chr6:125961194 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.201+4016G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961194 | ||||||
chr6:125961206 | C | A | 1 | a0002c0002t0002g0041 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.201+4028C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961206 | ||||||
chr6:125961388 | A | G | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.201+4210A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961388 | ||||||
chr6:125961459 | T | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(172): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.201+4281T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961459 | ||||||
chr6:125961478 | C | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0183 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.201+4300C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961478 | ||||||
chr6:125961764 | T | C | 1 | a0002c0002t0002g0042 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.201+4586T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961764 | ||||||
chr6:125961765 | C | T | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.201+4587C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125961765 | ||||||
chr6:125961985 | CCTGACTT others(63): Show |
C | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.201+4809_202-4831d others(72): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125961985 | |||||
chr6:125962149 | C | CATATATA others(19): Show |
2 | a0002c0002t0002g0013a0002c0002t0002g0014 | 4 | HG01069.hp1 HG01071.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-4702_202-4677d others(28): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962149 | |||||
chr6:125962155 | T | C | 2 | a0001c0001t0008g0087a0001c0001t0008g0089 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.202-4732T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962155 | ||||||
chr6:125962159 | TACACATA others(87): Show |
T | 2 | a0001c0001t0003g0099a0001c0001t0003g0200 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.202-4724_202-4631d others(96): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962159 | |||||
chr6:125962160 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-4727A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962160 | ||||||
chr6:125962161 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-4726C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962161 | ||||||
chr6:125962161 | CACATAT | C | 17 | a0001c0001t0001g0182a0002c0002t0001g0008a0002c0002t0001g0030others(14): Show | 20 | HG00280.hp2 HG00642.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.202-4724_202-4719d others(8): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | |||||
chr6:125962161 | CACATATA others(1): Show |
C | 74 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(71): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.202-4724_202-4717d others(10): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | |||||
chr6:125962161 | CACATATA others(3): Show |
C | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0020others(49): Show | 61 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.202-4724_202-4715d others(12): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | |||||
chr6:125962161 | CACATATA others(5): Show |
C | 2 | a0001c0001t0001g0025a0001c0001t0001g0172 | 3 | HG01515.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.202-4724_202-4713d others(14): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | |||||
chr6:125962161 | CACATATA others(7): Show |
C | 1 | a0001c0001t0001g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.202-4724_202-4711d others(16): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | |||||
chr6:125962161 | CACATATA others(25): Show |
C | 11 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0061others(8): Show | 16 | HG00609.hp1 HG00738.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.202-4724_202-4693d others(34): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | |||||
chr6:125962161 | CACATATA others(27): Show |
C | 1 | a0002c0002t0002g0005 | 3 | HG02965.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.202-4724_202-4691d others(36): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | |||||
chr6:125962161 | CACATATA others(89): Show |
C | 1 | a0001c0001t0018g0031 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.202-4724_202-4629d others(98): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | |||||
chr6:125962161 | CACATATA others(146): Show |
C | 2 | a0001c0001t0001g0192a0001c0004t0001g0193 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.202-4724_202-4572d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962161 | |||||
chr6:125962163 | C | CAT | 2 | a0002c0002t0002g0016a0002c0002t0002g0059 | 3 | HG00738.hp2 HG01167.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.202-4702_202-4701d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962163 | |||||
chr6:125962163 | C | T | 31 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0033others(28): Show | 35 | HG00099.hp2 HG01074.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.202-4724C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962163 | ||||||
chr6:125962165 | TATATATA others(17): Show |
T | 5 | a0002c0002t0002g0010a0002c0002t0002g0043a0002c0002t0002g0044others(2): Show | 6 | HG02258.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-4660_202-4637d others(26): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962165 | |||||
chr6:125962167 | T | C | 2 | a0001c0001t0008g0087a0001c0001t0008g0089 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.202-4720T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962167 | ||||||
chr6:125962167 | TATATATA others(15): Show |
T | 1 | a0002c0002t0002g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.202-4700_202-4679d others(24): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962167 | |||||
chr6:125962171 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-4716T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962171 | ||||||
chr6:125962177 | T | C | 29 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0033others(26): Show | 33 | HG00099.hp2 HG01074.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.202-4710T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962177 | ||||||
chr6:125962179 | T | C | 29 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0033others(26): Show | 33 | HG00099.hp2 HG01074.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.202-4708T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962179 | ||||||
chr6:125962181 | T | C | 2 | a0001c0001t0001g0124a0002c0002t0001g0079 | 2 | HG00099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.202-4706T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962181 | ||||||
chr6:125962183 | T | C | 16 | a0001c0001t0001g0123a0002c0002t0001g0008a0002c0002t0001g0030others(13): Show | 19 | HG00280.hp2 HG00558.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.202-4704T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962183 | ||||||
chr6:125962183 | TATACAC | T | 14 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0034others(11): Show | 17 | HG01074.hp2 HG02080.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.202-4700_202-4695d others(8): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962183 | |||||
chr6:125962185 | T | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(68): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.202-4702T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962185 | ||||||
chr6:125962185 | TACAC | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0090a0001c0001t0001g0119others(7): Show | 11 | HG00099.hp2 HG02258.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.202-4700_202-4697d others(6): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962185 | |||||
chr6:125962185 | TACACATA others(120): Show |
T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.202-4700_202-4574d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962185 | |||||
chr6:125962187 | C | T | 6 | a0001c0001t0001g0088a0001c0001t0001g0098a0001c0001t0003g0196others(3): Show | 6 | HG00639.hp1 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-4700C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962187 | ||||||
chr6:125962189 | C | CAT | 2 | a0002c0002t0002g0015a0002c0002t0002g0216 | 3 | HG01515.hp2 HG01517.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.202-4678_202-4677d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962189 | |||||
chr6:125962189 | C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(69): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.202-4698C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962189 | ||||||
chr6:125962191 | TATATATA others(15): Show |
T | 2 | a0002c0002t0002g0042a0002c0002t0002g0055 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.202-4676_202-4655d others(24): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962191 | |||||
chr6:125962193 | TATATATA others(13): Show |
T | 1 | a0002c0002t0002g0057 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.202-4676_202-4657d others(22): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962193 | |||||
chr6:125962198 | A | G | 2 | a0001c0001t0003g0197a0001c0001t0003g0198 | 2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.202-4689A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962198 | ||||||
chr6:125962199 | TATATATA others(106): Show |
T | 1 | a0001c0001t0008g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.202-4676_202-4564d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962199 | |||||
chr6:125962201 | TATATATA others(104): Show |
T | 1 | a0001c0001t0008g0089 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.202-4676_202-4566d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962201 | |||||
chr6:125962203 | TATATATA others(102): Show |
T | 3 | a0001c0001t0003g0095a0001c0001t0004g0217a0001c0001t0012g0040 | 3 | HG02922.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.202-4676_202-4568d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962203 | |||||
chr6:125962205 | TATATACA others(100): Show |
T | 2 | a0002c0002t0004g0209a0002c0002t0004g0210 | 2 | HG01192.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.202-4676_202-4570d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962205 | |||||
chr6:125962207 | T | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0172a0002c0002t0002g0068 | 4 | HG01515.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-4680T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962207 | ||||||
chr6:125962207 | TATACACA others(98): Show |
T | 8 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0098others(5): Show | 8 | HG02055.hp1 HG02630.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-4676_202-4572d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962207 | |||||
chr6:125962209 | T | C | 15 | a0001c0001t0001g0025a0001c0001t0001g0172a0002c0002t0002g0002others(12): Show | 23 | HG00609.hp1 HG00738.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-4678T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962209 | ||||||
chr6:125962209 | TACAC | T | 4 | a0001c0001t0003g0195a0001c0001t0003g0201a0001c0001t0003g0202others(1): Show | 4 | HG02145.hp2 HG02647.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-4676_202-4673d others(6): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962209 | |||||
chr6:125962209 | TACACATA others(92): Show |
T | 5 | a0001c0001t0003g0028a0001c0001t0003g0205a0002c0002t0004g0027others(2): Show | 6 | HG02486.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-4655_202-4557d others(101): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962209 | |||||
chr6:125962209 | TACACATA others(94): Show |
T | 2 | a0001c0001t0003g0213a0001c0001t0004g0212 | 2 | HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.202-4674_202-4574d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962209 | |||||
chr6:125962209 | TACACATA others(96): Show |
T | 12 | a0001c0001t0001g0018a0001c0001t0001g0100a0001c0001t0003g0196others(9): Show | 13 | HG00741.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.202-4676_202-4574d others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962209 | |||||
chr6:125962211 | C | T | 47 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0020others(44): Show | 56 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.202-4676C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962211 | ||||||
chr6:125962213 | C | CAT | 4 | a0002c0002t0002g0004a0002c0002t0002g0053a0002c0002t0002g0086others(1): Show | 7 | HG00323.hp2 HG02523.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-4654_202-4653d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962213 | |||||
chr6:125962213 | C | CATATATA others(61): Show |
1 | a0002c0002t0002g0054 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.202-4653_202-4652i others(70): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962213 | |||||
chr6:125962213 | C | T | 15 | a0001c0001t0001g0025a0001c0001t0001g0172a0002c0002t0002g0002others(12): Show | 23 | HG00609.hp1 HG00738.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-4674C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962213 | ||||||
chr6:125962213 | CAT | C | 4 | a0002c0002t0002g0047a0002c0002t0002g0048a0002c0002t0002g0049others(1): Show | 4 | HG01074.hp1 HG02698.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-4654_202-4653d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962213 | |||||
chr6:125962215 | T | C | 47 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0020others(44): Show | 56 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.202-4672T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962215 | ||||||
chr6:125962215 | T | TATATATA others(41): Show |
1 | a0002c0002t0002g0216 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.202-4653_202-4652i others(50): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962215 | |||||
chr6:125962217 | TATATATA others(51): Show |
T | 2 | a0001c0001t0001g0171a0001c0001t0001g0183 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.202-4658_202-4601d others(60): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962217 | |||||
chr6:125962219 | TATATATA others(11): Show |
T | 3 | a0002c0002t0002g0017a0002c0002t0002g0066a0002c0002t0002g0069 | 4 | HG02717.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-4654_202-4637d others(20): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962219 | |||||
chr6:125962219 | TATATATA others(49): Show |
T | 6 | a0001c0001t0001g0127a0001c0001t0001g0144a0002c0002t0001g0080others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-4656_202-4601d others(58): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962219 | |||||
chr6:125962219 | TATATATA others(86): Show |
T | 2 | a0001c0001t0003g0202a0001c0001t0003g0203 | 2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.202-4652_202-4560d others(95): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962219 | |||||
chr6:125962221 | TATATATA others(47): Show |
T | 68 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0026others(65): Show | 77 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(74): Show |
intron_variant | MODIFIER | c.202-4654_202-4601d others(56): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962221 | |||||
chr6:125962225 | TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.202-4652_202-4641d others(14): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962225 | |||||
chr6:125962225 | TATATATA others(80): Show |
T | 2 | a0001c0001t0003g0195a0001c0001t0003g0201 | 2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.202-4652_202-4566d others(89): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962225 | |||||
chr6:125962227 | TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.202-4652_202-4643d others(12): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962227 | |||||
chr6:125962231 | T | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0109 | 2 | HG02683.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.202-4656T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962231 | ||||||
chr6:125962233 | T | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0020others(40): Show | 52 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.202-4654T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962233 | ||||||
chr6:125962233 | T | TAC | 3 | a0002c0002t0002g0014a0002c0002t0002g0060a0002c0002t0002g0073 | 4 | HG00639.hp1 HG01192.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-4650_202-4649d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962233 | |||||
chr6:125962235 | C | T | 7 | a0001c0001t0001g0126a0001c0001t0001g0160a0001c0001t0001g0161others(4): Show | 7 | HG00280.hp1 HG00323.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-4652C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962235 | ||||||
chr6:125962235 | CACATATA others(43): Show |
C | 2 | a0001c0001t0001g0129a0001c0001t0001g0157 | 2 | HG02074.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.202-4648_202-4599d others(52): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962235 | |||||
chr6:125962237 | C | T | 1 | a0002c0002t0002g0071 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.202-4650C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962237 | ||||||
chr6:125962237 | CATATATA others(74): Show |
C | 2 | a0001c0001t0001g0025a0001c0001t0001g0172 | 3 | HG01515.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.202-4637_202-4557d others(83): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962237 | |||||
chr6:125962239 | T | C | 8 | a0001c0001t0001g0126a0001c0001t0001g0160a0001c0001t0001g0161others(5): Show | 8 | HG00280.hp1 HG00323.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-4648T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962239 | ||||||
chr6:125962239 | T | TATATATA others(83): Show |
1 | a0002c0002t0002g0015 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.202-4637_202-4636i others(92): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962239 | |||||
chr6:125962239 | TATATATA others(9): Show |
T | 1 | a0002c0002t0002g0070 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.202-4636_202-4621d others(18): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962239 | |||||
chr6:125962241 | TATATATA others(41): Show |
T | 38 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0020others(35): Show | 46 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.202-4636_202-4589d others(50): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962241 | |||||
chr6:125962243 | TATATATA others(39): Show |
T | 1 | a0002c0002t0001g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.202-4636_202-4591d others(48): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962243 | |||||
chr6:125962247 | TATACACA others(21): Show |
T | 7 | a0001c0001t0001g0126a0001c0001t0001g0160a0001c0001t0001g0161others(4): Show | 7 | HG00280.hp1 HG00323.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-4636_202-4609d others(30): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962247 | |||||
chr6:125962251 | C | T | 1 | a0002c0002t0002g0015 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.202-4636C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962251 | ||||||
chr6:125962255 | C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0164 | 2 | HG02735.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.202-4632C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962255 | ||||||
chr6:125962255 | CAT | C | 3 | a0002c0002t0002g0054a0002c0002t0002g0059a0002c0002t0002g0216 | 3 | HG01256.hp2 HG01981.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.202-4618_202-4617d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962255 | |||||
chr6:125962257 | T | C | 1 | a0002c0002t0002g0015 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.202-4630T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962257 | ||||||
chr6:125962269 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.202-4618T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962269 | ||||||
chr6:125962271 | CATACATA others(38): Show |
C | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.202-4612_202-4568d others(47): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962271 | |||||
chr6:125962271 | CATACATA others(40): Show |
C | 1 | a0001c0001t0001g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.202-4612_202-4566d others(49): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962271 | |||||
chr6:125962273 | T | C | 5 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0003g0099others(2): Show | 5 | HG01243.hp1 HG02735.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-4614T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962273 | ||||||
chr6:125962279 | TATATATA others(3): Show |
T | 2 | a0001c0001t0001g0159a0001c0001t0001g0164 | 2 | HG02735.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.202-4600_202-4591d others(12): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962279 | |||||
chr6:125962285 | T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0026others(61): Show | 70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.202-4602T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962285 | ||||||
chr6:125962289 | CAT | C | 8 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0016others(5): Show | 14 | HG00738.hp1 HG00738.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.202-4581_202-4580d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962289 | |||||
chr6:125962291 | T | C | 2 | a0001c0001t0001g0144a0002c0002t0002g0061 | 2 | HG00609.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.202-4596T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962291 | ||||||
chr6:125962306 | AT | A | 11 | a0001c0001t0001g0159a0001c0001t0001g0165a0002c0002t0001g0030others(8): Show | 12 | HG00280.hp2 HG00642.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-4580delT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962306 | ||||||
chr6:125962307 | T | A | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-4580T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962307 | ||||||
chr6:125962307 | TC | T | 60 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0020others(57): Show | 70 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.202-4579delC | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962307 | ||||||
chr6:125962307 | TCAC | T | 12 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0125others(9): Show | 12 | HG01074.hp2 HG02080.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-4579_202-4577d others(5): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962307 | ||||||
chr6:125962307 | TCACAC | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0026others(42): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.202-4579_202-4575d others(7): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962307 | ||||||
chr6:125962308 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-4579C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962308 | ||||||
chr6:125962310 | C | T | 6 | a0001c0001t0001g0108a0001c0001t0003g0028a0001c0001t0003g0205others(3): Show | 7 | HG02486.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-4577C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962310 | ||||||
chr6:125962312 | C | T | 20 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0108others(17): Show | 21 | HG01074.hp2 HG02080.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.202-4575C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962312 | ||||||
chr6:125962312 | CAT | C | 18 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(15): Show | 26 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.202-4558_202-4557d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962312 | |||||
chr6:125962312 | CATATAT | C | 71 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0020others(68): Show | 82 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.202-4562_202-4557d others(8): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125962312 | |||||
chr6:125962316 | T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0026others(50): Show | 59 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.202-4571T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962316 | ||||||
chr6:125962318 | T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0026others(53): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.202-4569T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962318 | ||||||
chr6:125962320 | T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0156 | 2 | HG01070.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.202-4567T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962320 | ||||||
chr6:125962343 | A | T | 3 | a0001c0001t0008g0087a0001c0001t0008g0089a0001c0001t0012g0040 | 3 | HG02976.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.202-4544A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962343 | ||||||
chr6:125962345 | C | T | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-4542C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962345 | ||||||
chr6:125962374 | C | T | 2 | a0001c0001t0008g0087a0001c0001t0008g0089 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.202-4513C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962374 | ||||||
chr6:125962396 | G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(172): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.202-4491G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962396 | ||||||
chr6:125962490 | C | T | 3 | a0001c0001t0008g0087a0001c0001t0008g0089a0001c0001t0012g0040 | 3 | HG02976.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.202-4397C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962490 | ||||||
chr6:125962498 | C | T | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-4389C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962498 | ||||||
chr6:125962534 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.202-4353C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962534 | ||||||
chr6:125962628 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.202-4259T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962628 | ||||||
chr6:125962759 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-4128G>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125962759 | ||||||
chr6:125963067 | A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(220): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.202-3820A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963067 | ||||||
chr6:125963123 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-3764A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963123 | ||||||
chr6:125963253 | G | A | 6 | a0002c0002t0002g0013a0002c0002t0002g0014a0002c0002t0002g0060others(3): Show | 8 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-3634G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963253 | ||||||
chr6:125963255 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-3632T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963255 | ||||||
chr6:125963258 | T | A | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-3629T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963258 | ||||||
chr6:125963262 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-3625A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963262 | ||||||
chr6:125963350 | A | T | 1 | a0002c0002t0002g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.202-3537A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963350 | ||||||
chr6:125963521 | C | T | 2 | a0001c0001t0008g0087a0001c0001t0008g0089 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.202-3366C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963521 | ||||||
chr6:125963687 | A | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0090others(3): Show | 7 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-3200A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963687 | ||||||
chr6:125963709 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.202-3178A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963709 | ||||||
chr6:125963820 | T | C | 5 | a0002c0002t0004g0027a0002c0002t0004g0204a0002c0002t0004g0209others(2): Show | 6 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-3067T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963820 | ||||||
chr6:125963942 | C | G | 1 | a0001c0001t0008g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.202-2945C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125963942 | ||||||
chr6:125964064 | A | G | 1 | a0001c0001t0011g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-2823A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964064 | ||||||
chr6:125964101 | C | A | 1 | a0002c0002t0002g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.202-2786C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964101 | ||||||
chr6:125964187 | A | G | 21 | a0001c0001t0003g0028a0001c0001t0003g0200a0001c0001t0003g0201others(18): Show | 22 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.202-2700A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964187 | ||||||
chr6:125964195 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.202-2692C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964195 | ||||||
chr6:125964323 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.202-2564T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964323 | ||||||
chr6:125964395 | G | GT | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(172): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.202-2491dupT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964395 | |||||
chr6:125964453 | A | G | 1 | a0002c0002t0001g0221 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.202-2434A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964453 | ||||||
chr6:125964597 | A | G | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-2290A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964597 | ||||||
chr6:125964737 | T | TAC | 4 | a0002c0002t0002g0013a0002c0002t0002g0042a0002c0002t0002g0060others(1): Show | 5 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-2112_202-2111d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | |||||
chr6:125964737 | T | TACAC | 2 | a0002c0002t0002g0005a0002c0002t0002g0073 | 4 | HG01192.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-2114_202-2111d others(6): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | |||||
chr6:125964737 | TAC | T | 11 | a0001c0001t0001g0100a0001c0001t0001g0192a0001c0001t0003g0099others(8): Show | 12 | HG00609.hp1 HG00741.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-2112_202-2111d others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | |||||
chr6:125964737 | TACAC | T | 8 | a0001c0001t0001g0183a0001c0001t0011g0194a0001c0001t0018g0031others(5): Show | 13 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.202-2114_202-2111d others(6): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | |||||
chr6:125964737 | TACACAC | T | 22 | a0001c0001t0003g0028a0001c0001t0003g0095a0001c0001t0003g0200others(19): Show | 23 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.202-2116_202-2111d others(8): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | |||||
chr6:125964737 | TACACACA others(1): Show |
T | 30 | a0001c0001t0001g0114a0001c0001t0001g0143a0001c0001t0001g0155others(27): Show | 33 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.202-2118_202-2111d others(10): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | |||||
chr6:125964737 | TACACACA others(3): Show |
T | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(104): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.202-2120_202-2111d others(12): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | |||||
chr6:125964737 | TACACACA others(5): Show |
T | 5 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0090others(2): Show | 6 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-2122_202-2111d others(14): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 125964737 | |||||
chr6:125964739 | CACACACA others(4): Show |
C | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-2147_202-2137d others(13): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964739 | ||||||
chr6:125964799 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.202-2088G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964799 | ||||||
chr6:125964799 | G | T | 1 | a0001c0001t0008g0089 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.202-2088G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964799 | ||||||
chr6:125964877 | A | G | 1 | a0001c0001t0003g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.202-2010A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964877 | ||||||
chr6:125964969 | C | G | 1 | a0002c0002t0001g0085 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.202-1918C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125964969 | ||||||
chr6:125965026 | A | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0153a0001c0001t0001g0154others(1): Show | 4 | HG00621.hp2 HG02523.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-1861A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125965026 | ||||||
chr6:125965427 | T | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0145 | 2 | HG02080.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.202-1460T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125965427 | ||||||
chr6:125965441 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.202-1446T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125965441 | ||||||
chr6:125965670 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.202-1217T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125965670 | ||||||
chr6:125965743 | C | A | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-1144C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125965743 | ||||||
chr6:125965909 | A | G | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-978A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125965909 | ||||||
chr6:125966005 | T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(222): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.202-882T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966005 | ||||||
chr6:125966008 | G | A | 1 | a0001c0004t0001g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.202-879G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966008 | ||||||
chr6:125966012 | C | T | 4 | a0001c0001t0003g0095a0001c0001t0005g0092a0001c0001t0005g0093others(1): Show | 4 | HG02895.hp1 HG02922.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-875C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966012 | ||||||
chr6:125966080 | G | A | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-807G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966080 | ||||||
chr6:125966084 | A | G | 2 | a0001c0001t0008g0087a0001c0001t0008g0089 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.202-803A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966084 | ||||||
chr6:125966112 | T | C | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-775T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966112 | ||||||
chr6:125966115 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-772A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966115 | ||||||
chr6:125966118 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-769A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966118 | ||||||
chr6:125966291 | G | T | 3 | a0001c0001t0008g0087a0001c0001t0008g0089a0001c0001t0012g0040 | 3 | HG02976.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.202-596G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966291 | ||||||
chr6:125966444 | C | T | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-443C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966444 | ||||||
chr6:125966560 | G | GA | 3 | a0001c0001t0008g0087a0001c0001t0008g0089a0001c0001t0012g0040 | 3 | HG02976.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.202-327_202-326ins others(1): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966560 | ||||||
chr6:125966582 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-305A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966582 | ||||||
chr6:125966767 | G | T | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-120G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966767 | ||||||
chr6:125966777 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-110A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966777 | ||||||
chr6:125966779 | A | G | 5 | a0002c0002t0002g0017a0002c0002t0002g0066a0002c0002t0002g0069others(2): Show | 6 | HG02647.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-108A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966779 | ||||||
chr6:125966780 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-107T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966780 | ||||||
chr6:125966854 | T | A | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-33T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966854 | ||||||
chr6:125966855 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-32A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966855 | ||||||
chr6:125966858 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202-29A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966858 | ||||||
chr6:125966877 | T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.202-10T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 1/4 | chr6 | 125966877 | ||||||
chr6:125967009 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA19066.hp1 | splice_region_variant&intron_variant | LOW | c.319+5G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967009 | ||||||
chr6:125967052 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.319+48A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967052 | ||||||
chr6:125967221 | A | T | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.319+217A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967221 | ||||||
chr6:125967225 | T | A | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.319+221T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967225 | ||||||
chr6:125967326 | CT | C | 10 | a0001c0001t0001g0108a0001c0001t0001g0115a0001c0001t0001g0133others(7): Show | 10 | HG00099.hp1 HG00323.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.319+345delT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125967326 | |||||
chr6:125967326 | CTT | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(152): Show | 173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.319+344_319+345del others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125967326 | |||||
chr6:125967326 | CTTT | C | 10 | a0001c0001t0001g0088a0001c0001t0001g0098a0001c0001t0001g0111others(7): Show | 11 | HG02258.hp1 HG02615.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.319+343_319+345del others(3): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125967326 | |||||
chr6:125967466 | G | T | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.319+462G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967466 | ||||||
chr6:125967524 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.319+520G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967524 | ||||||
chr6:125967601 | G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0155 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.319+597G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967601 | ||||||
chr6:125967772 | A | T | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.319+768A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967772 | ||||||
chr6:125967880 | C | G | 1 | a0002c0002t0002g0060 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.319+876C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967880 | ||||||
chr6:125967993 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.319+989G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125967993 | ||||||
chr6:125968151 | C | T | 1 | a0002c0002t0002g0045 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.319+1147C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968151 | ||||||
chr6:125968301 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.319+1297A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968301 | ||||||
chr6:125968324 | T | C | 1 | a0001c0001t0008g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.319+1320T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968324 | ||||||
chr6:125968366 | G | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.319+1362G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968366 | ||||||
chr6:125968800 | C | T | 1 | a0002c0002t0002g0063 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.319+1796C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968800 | ||||||
chr6:125968845 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.319+1841A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968845 | ||||||
chr6:125968882 | A | G | 3 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0205 | 3 | HG02622.hp1 HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.319+1878A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125968882 | ||||||
chr6:125969058 | C | T | 4 | a0002c0002t0002g0010a0002c0002t0002g0044a0002c0002t0002g0045others(1): Show | 5 | HG02451.hp1 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.319+2054C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969058 | ||||||
chr6:125969115 | C | T | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.319+2111C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969115 | ||||||
chr6:125969119 | A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(91): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.319+2115A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969119 | ||||||
chr6:125969189 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.319+2185A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969189 | ||||||
chr6:125969263 | G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0090 | 3 | HG02896.hp2 HG02897.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.319+2259G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969263 | ||||||
chr6:125969265 | A | G | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.319+2261A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969265 | ||||||
chr6:125969319 | A | G | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.319+2315A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969319 | ||||||
chr6:125969396 | T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(166): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.319+2392T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969396 | ||||||
chr6:125969408 | C | T | 3 | a0001c0001t0004g0214a0001c0001t0004g0215a0001c0001t0004g0217 | 3 | HG03041.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.319+2404C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969408 | ||||||
chr6:125969488 | T | G | 1 | a0002c0002t0002g0223 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.319+2484T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969488 | ||||||
chr6:125969551 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.319+2547G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969551 | ||||||
chr6:125969573 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.319+2569T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969573 | ||||||
chr6:125969635 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.320-2624C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969635 | ||||||
chr6:125969636 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.320-2623A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969636 | ||||||
chr6:125969637 | T | A | 1 | a0001c0001t0001g0108 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.320-2622T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969637 | ||||||
chr6:125969644 | G | A | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.320-2615G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969644 | ||||||
chr6:125969846 | C | T | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.320-2413C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969846 | ||||||
chr6:125969911 | G | A | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.320-2348G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125969911 | ||||||
chr6:125970123 | A | G | 2 | a0001c0001t0008g0087a0001c0001t0008g0089 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.320-2136A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125970123 | ||||||
chr6:125970330 | T | C | 1 | a0002c0002t0002g0074 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.320-1929T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125970330 | ||||||
chr6:125970762 | G | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(171): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.320-1497G>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125970762 | ||||||
chr6:125970950 | A | G | 4 | a0001c0001t0003g0195a0001c0001t0003g0196a0001c0001t0003g0197others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.320-1309A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125970950 | ||||||
chr6:125970968 | A | G | 1 | a0001c0001t0011g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.320-1291A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125970968 | ||||||
chr6:125970996 | A | C | 1 | a0001c0001t0001g0140 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.320-1263A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125970996 | ||||||
chr6:125971041 | G | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(201): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.320-1218G>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971041 | ||||||
chr6:125971155 | C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.320-1104C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971155 | ||||||
chr6:125971269 | C | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0151 | 3 | HG00408.hp2 NA19066.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.320-990C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971269 | ||||||
chr6:125971318 | T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(171): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.320-941T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971318 | ||||||
chr6:125971676 | A | G | 1 | a0002c0002t0002g0005 | 3 | HG02965.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.320-583A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971676 | ||||||
chr6:125971688 | C | G | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.320-571C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971688 | ||||||
chr6:125971702 | C | CT | 40 | a0001c0001t0001g0088a0001c0001t0001g0098a0001c0001t0001g0162others(37): Show | 42 | HG00609.hp1 HG00642.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.320-531dupT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125971702 | |||||
chr6:125971702 | C | CTT | 99 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(96): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.320-532_320-531dup others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125971702 | |||||
chr6:125971702 | C | CTTT | 23 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0037others(20): Show | 24 | HG00597.hp1 HG00597.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.320-533_320-531dup others(3): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125971702 | |||||
chr6:125971702 | C | CTTTT | 17 | a0001c0001t0001g0034a0001c0001t0001g0124a0001c0001t0001g0171others(14): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.320-534_320-531dup others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125971702 | |||||
chr6:125971702 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0137a0001c0001t0001g0173 | 2 | HG00639.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.320-544_320-531del others(14): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 125971702 | |||||
chr6:125971866 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.320-393C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 2/4 | chr6 | 125971866 | ||||||
chr6:125972365 | T | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0183 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.389+37T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972365 | ||||||
chr6:125972493 | C | T | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.389+165C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972493 | ||||||
chr6:125972507 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.389+179A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972507 | ||||||
chr6:125972593 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.389+265T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972593 | ||||||
chr6:125972639 | G | T | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.389+311G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972639 | ||||||
chr6:125972749 | G | A | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.389+421G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972749 | ||||||
chr6:125972899 | T | C | 1 | a0002c0002t0001g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.389+571T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972899 | ||||||
chr6:125972932 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.389+604T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125972932 | ||||||
chr6:125973065 | C | CT | 7 | a0001c0001t0001g0115a0001c0001t0001g0134a0001c0001t0001g0180others(4): Show | 7 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+765dupT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 125973065 | |||||
chr6:125973065 | C | CTT | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(85): Show | 102 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.389+764_389+765dup others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 125973065 | |||||
chr6:125973065 | C | CTTT | 59 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0033others(56): Show | 63 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.389+763_389+765dup others(3): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 125973065 | |||||
chr6:125973065 | C | CTTTT | 15 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0037others(12): Show | 16 | HG01069.hp2 HG01109.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.389+762_389+765dup others(4): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 125973065 | |||||
chr6:125973078 | T | G | 1 | a0002c0002t0002g0068 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.389+750T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973078 | ||||||
chr6:125973154 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.389+826C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973154 | ||||||
chr6:125973168 | G | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(172): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.389+840G>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973168 | ||||||
chr6:125973217 | G | A | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.389+889G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973217 | ||||||
chr6:125973299 | G | A | 1 | a0002c0002t0002g0047 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.389+971G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973299 | ||||||
chr6:125973303 | T | C | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.389+975T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973303 | ||||||
chr6:125973321 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.389+993C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973321 | ||||||
chr6:125973361 | G | A | 1 | a0002c0002t0001g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.389+1033G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973361 | ||||||
chr6:125973426 | G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(172): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.389+1098G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973426 | ||||||
chr6:125973556 | G | A | 1 | a0001c0001t0003g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.389+1228G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973556 | ||||||
chr6:125973562 | A | G | 2 | a0001c0001t0001g0192a0001c0004t0001g0193 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.389+1234A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973562 | ||||||
chr6:125973594 | G | C | 1 | a0002c0002t0002g0053 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.390-1253G>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973594 | ||||||
chr6:125973834 | G | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(172): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.390-1013G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973834 | ||||||
chr6:125973882 | T | C | 1 | a0001c0001t0018g0031 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.390-965T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973882 | ||||||
chr6:125973951 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.390-896G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125973951 | ||||||
chr6:125974138 | G | A | 8 | a0001c0001t0003g0095a0001c0001t0003g0195a0001c0001t0003g0196others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.390-709G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974138 | ||||||
chr6:125974153 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.390-694T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974153 | ||||||
chr6:125974189 | A | G | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.390-658A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974189 | ||||||
chr6:125974336 | A | C | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.390-511A>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974336 | ||||||
chr6:125974340 | C | T | 2 | a0002c0002t0009g0052a0002c0002t0009g0056 | 2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.390-507C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974340 | ||||||
chr6:125974365 | T | C | 2 | a0002c0002t0002g0060a0002c0002t0002g0073 | 2 | HG00639.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.390-482T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974365 | ||||||
chr6:125974399 | G | GA | 7 | a0001c0001t0001g0112a0001c0001t0001g0189a0002c0002t0004g0027others(4): Show | 8 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.390-445dupA | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 125974399 | |||||
chr6:125974540 | C | A | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.390-307C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974540 | ||||||
chr6:125974599 | T | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(172): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.390-248T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974599 | ||||||
chr6:125974786 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.390-61C>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 3/4 | chr6 | 125974786 | ||||||
chr6:125975105 | A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0156 | 2 | HG01070.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.516+132A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975105 | ||||||
chr6:125975178 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.516+205A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975178 | ||||||
chr6:125975200 | C | G | 11 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0003g0091others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.516+227C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975200 | ||||||
chr6:125975463 | A | G | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0005g0094 | 3 | HG02895.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.516+490A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975463 | ||||||
chr6:125975524 | A | G | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.516+551A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975524 | ||||||
chr6:125975575 | T | C | 17 | a0002c0002t0001g0008a0002c0002t0001g0030a0002c0002t0001g0076others(14): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.516+602T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975575 | ||||||
chr6:125975581 | G | GT | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(155): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.516+610dupT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 125975581 | |||||
chr6:125975581 | G | GTT | 12 | a0001c0001t0001g0096a0001c0001t0001g0114a0001c0001t0001g0123others(9): Show | 12 | HG00558.hp1 HG01175.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.516+609_516+610dup others(2): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 125975581 | |||||
chr6:125975584 | G | GTTTTTTT | 6 | a0001c0001t0008g0087a0001c0001t0008g0089a0002c0002t0002g0017others(3): Show | 7 | HG02647.hp1 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.516+619_516+625dup others(7): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 125975584 | |||||
chr6:125975584 | G | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(170): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.516+611G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975584 | ||||||
chr6:125975586 | T | TTTGTTTT others(4): Show |
1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.516+615_516+616ins others(11): Show |
HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 125975586 | |||||
chr6:125975656 | C | T | 2 | a0001c0001t0008g0087a0001c0001t0008g0089 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.516+683C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975656 | ||||||
chr6:125975728 | C | G | 1 | a0001c0001t0003g0099 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.516+755C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975728 | ||||||
chr6:125975765 | A | G | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.516+792A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125975765 | ||||||
chr6:125976110 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.516+1137A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976110 | ||||||
chr6:125976142 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.516+1169A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976142 | ||||||
chr6:125976235 | C | T | 3 | a0001c0001t0008g0087a0001c0001t0008g0089a0001c0001t0012g0040 | 3 | HG02976.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.516+1262C>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976235 | ||||||
chr6:125976399 | T | G | 1 | a0001c0001t0001g0125 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.517-1245T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976399 | ||||||
chr6:125976454 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.517-1190A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976454 | ||||||
chr6:125976517 | G | GT | 20 | a0001c0001t0001g0037a0001c0001t0001g0113a0001c0001t0001g0119others(17): Show | 20 | HG00642.hp2 HG01081.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.517-1111dupT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 125976517 | |||||
chr6:125976517 | GT | G | 10 | a0001c0001t0003g0028a0001c0001t0003g0200a0001c0001t0003g0201others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.517-1111delT | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 125976517 | |||||
chr6:125976558 | C | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1086C>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976558 | ||||||
chr6:125976559 | T | C | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1085T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976559 | ||||||
chr6:125976562 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1082T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976562 | ||||||
chr6:125976565 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1079T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976565 | ||||||
chr6:125976567 | T | A | 4 | a0001c0001t0003g0095a0001c0001t0005g0092a0001c0001t0005g0093others(1): Show | 4 | HG02895.hp1 HG02922.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-1077T>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976567 | ||||||
chr6:125976585 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1059T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976585 | ||||||
chr6:125976591 | T | C | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-1053T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976591 | ||||||
chr6:125976593 | A | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1051A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976593 | ||||||
chr6:125976594 | G | A | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1050G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976594 | ||||||
chr6:125976604 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1040T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976604 | ||||||
chr6:125976612 | A | T | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1032A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976612 | ||||||
chr6:125976614 | A | T | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1030A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976614 | ||||||
chr6:125976632 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1012T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976632 | ||||||
chr6:125976634 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-1010T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976634 | ||||||
chr6:125976654 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-990T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976654 | ||||||
chr6:125976659 | T | C | 9 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0123others(6): Show | 9 | HG00558.hp1 HG01255.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-985T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976659 | ||||||
chr6:125976661 | A | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-983A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976661 | ||||||
chr6:125976674 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-970T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976674 | ||||||
chr6:125976698 | A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(172): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.517-946A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976698 | ||||||
chr6:125976700 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-944T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976700 | ||||||
chr6:125976702 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-942T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976702 | ||||||
chr6:125976715 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-929T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976715 | ||||||
chr6:125976722 | A | T | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-922A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976722 | ||||||
chr6:125976724 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-920T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976724 | ||||||
chr6:125976728 | A | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-916A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976728 | ||||||
chr6:125976734 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-910T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976734 | ||||||
chr6:125976737 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-907T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976737 | ||||||
chr6:125976739 | A | T | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-905A>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976739 | ||||||
chr6:125976741 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-903T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976741 | ||||||
chr6:125976749 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-895T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976749 | ||||||
chr6:125976761 | T | G | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-883T>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976761 | ||||||
chr6:125976823 | T | C | 1 | a0001c0001t0004g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.517-821T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976823 | ||||||
chr6:125976922 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.517-722T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976922 | ||||||
chr6:125976949 | G | A | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-695G>A | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125976949 | ||||||
chr6:125977223 | T | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(172): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.517-421T>C | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125977223 | ||||||
chr6:125977275 | G | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(172): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.517-369G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125977275 | ||||||
chr6:125977368 | A | G | 1 | a0001c0001t0012g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-276A>G | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125977368 | ||||||
chr6:125977601 | G | T | 1 | a0001c0001t0003g0099 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.517-43G>T | HINT3 | ENSG00000111911.7 | transcript | ENST00000229633.7 | protein_coding | 4/4 | chr6 | 125977601 |