geneid | 3074 |
---|---|
ensemblid | ENSG00000049860.14 |
hgncid | 4879 |
symbol | HEXB |
name | hexosaminidase subunit beta |
refseq_nuc | NM_000521.4 |
refseq_prot | NP_000512.2 |
ensembl_nuc | ENST00000261416.12 |
ensembl_prot | ENSP00000261416.7 |
mane_status | MANE Select |
chr | chr5 |
start | 74685233 |
end | 74721288 |
strand | + |
ver | v1.2 |
region | chr5:74685233-74721288 |
region5000 | chr5:74680233-74726288 |
regionname0 | HEXB_chr5_74685233_74721288 |
regionname5000 | HEXB_chr5_74680233_74726288 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 556 | 237 | 62 | 38 | 97 | 7 | 32 | 67 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0002 | 0/0 | 556 | 89 | 28 | 18 | 30 | 4 | 9 | 26 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0003 | 0/0 | 556 | 54 | 1 | 12 | 35 | 2 | 4 | 28 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0004 | 1/0 | 556 | 5 | 0 | 2 | 0 | 1 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0005 | 0/0 | 556 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0006 | 0/0 | 556 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0007 | 0/0 | 556 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0008 | 0/0 | 556 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0009 | 0/0 | 556 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0010 | 0/0 | 556 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0011 | 0/0 | 556 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1671 | 231 | 56 | 38 | 97 | 7 | 32 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
c0002 | 0/0 | 1671 | 89 | 28 | 18 | 30 | 4 | 9 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
c0003 | 0/0 | 1671 | 54 | 1 | 12 | 35 | 2 | 4 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
c0004 | 0/0 | 1671 | 5 | 5 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
c0005 | 1/0 | 1671 | 5 | 0 | 2 | 0 | 1 | 1 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
c0006 | 0/0 | 1671 | 3 | 2 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
c0007 | 0/0 | 1671 | 3 | 2 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
c0008 | 0/0 | 1671 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
c0009 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
c0010 | 0/0 | 1671 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
c0011 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
c0012 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
c0013 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 142 | 357 | 95 | 66 | 138 | 13 | 43 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
t0002 | 0/0 | 140 | 38 | 1 | 6 | 27 | 1 | 3 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
t0003 | 0/0 | 142 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0005 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0007 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0035 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1671 | 231 | 56 | 38 | 97 | 7 | 32 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0001c0004 | 0/0 | 1671 | 5 | 5 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0001c0010 | 0/0 | 1671 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0002c0002 | 0/0 | 1671 | 89 | 28 | 18 | 30 | 4 | 9 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0003c0003 | 0/0 | 1671 | 54 | 1 | 12 | 35 | 2 | 4 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0004c0005 | 1/0 | 1671 | 5 | 0 | 2 | 0 | 1 | 1 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0005c0006 | 0/0 | 1671 | 3 | 2 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0006c0007 | 0/0 | 1671 | 3 | 2 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0007c0013 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0008c0009 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0009c0011 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0010c0008 | 0/0 | 1671 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0011c0012 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1812 | 224 | 55 | 38 | 94 | 6 | 30 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0001c0001t0002 | 0/0 | 1810 | 6 | 1 | 0 | 2 | 1 | 2 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0001c0001t0003 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0001c0004t0001 | 0/0 | 1812 | 5 | 5 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0001c0010t0001 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0002c0002t0001 | 0/0 | 1812 | 81 | 28 | 18 | 23 | 4 | 8 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0002c0002t0002 | 0/0 | 1810 | 8 | 0 | 0 | 7 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0003c0003t0001 | 0/0 | 1812 | 31 | 1 | 6 | 18 | 2 | 4 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0003c0003t0002 | 0/0 | 1810 | 23 | 0 | 6 | 17 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0004c0005t0001 | 1/0 | 1812 | 5 | 0 | 2 | 0 | 1 | 1 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0005c0006t0001 | 0/0 | 1812 | 3 | 2 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0006c0007t0001 | 0/0 | 1812 | 3 | 2 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0007c0013t0001 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0008c0009t0001 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0009c0011t0001 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0010c0008t0001 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
a0011c0012t0002 | 0/0 | 1810 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | copy fasta | chr5 | 74680233 | 74726288 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0004t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0004t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0001c0010t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0005 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0003c0003t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0004c0005t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0004c0005t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0004c0005t0001g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0004c0005t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0005c0006t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0005c0006t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0005c0006t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0006c0007t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0006c0007t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0006c0007t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0007c0013t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0008c0009t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0009c0011t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0010c0008t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
a0011c0012t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0035 | EUR | GBR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00099 | hp2 | a0004 | c0005 | t0001 | g0032 | EUR | GBR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | GBR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | GBR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | FIN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00280 | hp2 | a0003 | c0003 | t0001 | g0005 | EUR | FIN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0312 | EUR | FIN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00423 | hp1 | a0009 | c0011 | t0001 | g0194 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00423 | hp2 | a0003 | c0003 | t0001 | g0214 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00438 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00597 | hp1 | a0003 | c0003 | t0001 | g0180 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0324 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00642 | hp1 | a0006 | c0007 | t0001 | g0057 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00673 | hp1 | a0003 | c0003 | t0002 | g0187 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0303 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0277 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00738 | hp2 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00741 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01069 | hp2 | a0004 | c0005 | t0001 | g0250 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01071 | hp1 | a0004 | c0005 | t0001 | g0032 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0302 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0286 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01109 | hp2 | a0005 | c0006 | t0001 | g0042 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0285 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01175 | hp1 | a0003 | c0003 | t0002 | g0216 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0267 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0314 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01515 | hp1 | a0003 | c0003 | t0001 | g0005 | EUR | IBS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0295 | EUR | IBS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0291 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0006 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01928 | hp2 | a0003 | c0003 | t0001 | g0197 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01943 | hp1 | a0003 | c0003 | t0001 | g0186 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0276 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01975 | hp2 | a0003 | c0003 | t0001 | g0192 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0308 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0274 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0316 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0264 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0294 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02055 | hp1 | a0006 | c0007 | t0001 | g0178 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02055 | hp2 | a0006 | c0007 | t0001 | g0055 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02071 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02074 | hp2 | a0003 | c0003 | t0001 | g0183 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02132 | hp1 | a0003 | c0003 | t0001 | g0190 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0260 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02148 | hp2 | a0003 | c0003 | t0001 | g0217 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02155 | hp1 | a0008 | c0009 | t0001 | g0239 | EAS | CDX | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0271 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02273 | hp1 | a0003 | c0003 | t0002 | g0207 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0282 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0292 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02293 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02293 | hp2 | a0003 | c0003 | t0001 | g0211 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02300 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0036 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0268 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0275 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0287 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0293 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0266 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0279 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0269 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02647 | hp2 | a0001 | c0004 | t0001 | g0006 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0313 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02717 | hp2 | a0010 | c0008 | t0001 | g0051 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02809 | hp2 | a0001 | c0004 | t0001 | g0006 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02818 | hp2 | a0001 | c0010 | t0001 | g0061 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0319 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03041 | hp2 | a0005 | c0006 | t0001 | g0045 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03130 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0322 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0320 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03209 | hp2 | a0001 | c0004 | t0001 | g0218 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0317 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03490 | hp2 | a0003 | c0003 | t0001 | g0026 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0300 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0296 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03492 | hp2 | a0003 | c0003 | t0001 | g0026 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03516 | hp2 | a0005 | c0006 | t0001 | g0043 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0307 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0280 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0262 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03927 | hp1 | a0003 | c0003 | t0001 | g0199 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0273 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0272 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG04228 | hp2 | a0004 | c0005 | t0001 | g0031 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0284 | AFR | YRI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | YRI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18747 | hp1 | a0007 | c0013 | t0001 | g0021 | EAS | CHB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | YRI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | YRI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18939 | hp2 | a0003 | c0003 | t0001 | g0193 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18942 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18944 | hp1 | a0003 | c0003 | t0002 | g0025 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18946 | hp1 | a0003 | c0003 | t0002 | g0212 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18950 | hp2 | a0003 | c0003 | t0001 | g0213 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18954 | hp1 | a0003 | c0003 | t0001 | g0201 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0306 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18963 | hp2 | a0011 | c0012 | t0002 | g0011 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18964 | hp2 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18965 | hp1 | a0003 | c0003 | t0002 | g0185 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18966 | hp2 | a0003 | c0003 | t0002 | g0205 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18970 | hp2 | a0003 | c0003 | t0001 | g0209 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18971 | hp1 | a0003 | c0003 | t0001 | g0195 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0328 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0326 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18983 | hp1 | a0003 | c0003 | t0002 | g0200 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18986 | hp1 | a0003 | c0003 | t0002 | g0181 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18987 | hp1 | a0003 | c0003 | t0002 | g0184 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18994 | hp1 | a0003 | c0003 | t0002 | g0025 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18994 | hp2 | a0003 | c0003 | t0001 | g0198 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18995 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18999 | hp2 | a0003 | c0003 | t0001 | g0202 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19005 | hp1 | a0003 | c0003 | t0002 | g0203 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0315 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0288 | AFR | LWK | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0318 | AFR | LWK | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | LWK | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19056 | hp1 | a0003 | c0003 | t0002 | g0210 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0325 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19065 | hp1 | a0003 | c0003 | t0001 | g0024 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19074 | hp1 | a0003 | c0003 | t0002 | g0204 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19075 | hp1 | a0003 | c0003 | t0002 | g0206 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19076 | hp2 | a0003 | c0003 | t0001 | g0182 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19080 | hp1 | a0003 | c0003 | t0002 | g0196 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19087 | hp1 | a0003 | c0003 | t0002 | g0208 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19090 | hp1 | a0003 | c0003 | t0002 | g0188 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0290 | AFR | YRI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ASW | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ASW | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0299 | EUR | TSI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0173 | EUR | TSI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA20905 | hp1 | a0003 | c0003 | t0001 | g0005 | SAS | GIH | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | GIH | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01123 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0289 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | USA | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | USA | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA18955 | hp2 | a0003 | c0003 | t0001 | g0024 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | USA | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA20300 | hp2 | a0003 | c0003 | t0001 | g0189 | AFR | USA | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | LWK | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0099 | REF | REF | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
homoSapiens_grch38 | hp1 | a0004 | c0005 | t0001 | g0237 | REF | REF | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:74685445
|
T | C | 10 | a0001a0002a0003others(7): Show | 391 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(388): Show |
missense_variant | MODERATE | c.185T>C | p.Leu62Ser | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/14 | 213/1812 | 185/1671 | 62/556 | chr5 | 74685445 | ||
chr5:74685474
|
C | T | 1 | a0007 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.214C>T | p.Leu72Phe | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/14 | 242/1812 | 214/1671 | 72/556 | chr5 | 74685474 | ||
chr5:74689390
|
A | G | 2 | a0002a0011 | 90 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(87): Show |
missense_variant | MODERATE | c.362A>G | p.Lys121Arg | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/14 | 390/1812 | 362/1671 | 121/556 | chr5 | 74689390 | ||
chr5:74689411
|
T | G | 1 | a0010 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.383T>G | p.Leu128Arg | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/14 | 411/1812 | 383/1671 | 128/556 | chr5 | 74689411 | ||
chr5:74693642
|
C | A | 1 | a0005 | 3 | HG01109.hp2 HG03041.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.449C>A | p.Thr150Asn | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/14 | 477/1812 | 449/1671 | 150/556 | chr5 | 74693642 | ||
chr5:74697056
|
A | G | 2 | a0003a0009 | 55 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(52): Show |
missense_variant | MODERATE | c.619A>G | p.Ile207Val | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/14 | 647/1812 | 619/1671 | 207/556 | chr5 | 74697056 | ||
chr5:74713558
|
T | C | 1 | a0008 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.824T>C | p.Ile275Thr | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/14 | 852/1812 | 824/1671 | 275/556 | chr5 | 74713558 | ||
chr5:74715674
|
G | A | 1 | a0009 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.1066G>A | p.Val356Met | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/14 | 1094/1812 | 1066/1671 | 356/556 | chr5 | 74715674 | ||
chr5:74718804
|
C | T | 1 | a0011 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.1250C>T | p.Pro417Leu | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/14 | 1278/1812 | 1250/1671 | 417/556 | chr5 | 74718804 | ||
chr5:74718812
|
A | G | 1 | a0006 | 3 | HG00642.hp1 HG02055.hp1 HG02055.hp2 |
missense_variant | MODERATE | c.1258A>G | p.Ile420Val | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/14 | 1286/1812 | 1258/1671 | 420/556 | chr5 | 74718812 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:74685536
|
C | T | 1 | a0001c0004 | 5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
synonymous_variant | LOW | c.276C>T | p.Thr92Thr | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/14 | 304/1812 | 276/1671 | 92/556 | chr5 | 74685536 | ||
chr5:74715659
|
T | C | 1 | a0001c0010 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.1051T>C | p.Leu351Leu | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/14 | 1079/1812 | 1051/1671 | 351/556 | chr5 | 74715659 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:74721255
|
CTG | C | 4 | a0001c0001t0002a0002c0002t0002a0003c0003t0002others(1): Show | 38 | HG00673.hp1 HG00741.hp1 HG01123.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*82_*83delGT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 14/14 | 82 | INFO_REALIGN_3_PRIME | chr5 | 74721255 | ||||
chr5:74721282
|
G | A | 1 | a0001c0001t0003 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*107G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 14/14 | 107 | chr5 | 74721282 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:74685634
|
C | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.299+75C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74685634 | ||||||
chr5:74685837
|
G | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(188): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.299+278G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74685837 | ||||||
chr5:74686133
|
G | GTCAGTGG others(1): Show |
44 | a0001c0001t0001g0215a0003c0003t0001g0005a0003c0003t0001g0009others(41): Show | 56 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.299+576_299+583dup others(8): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 74686133 | |||||
chr5:74686254
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.299+695A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686254 | ||||||
chr5:74686500
|
C | A | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(192): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.299+941C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686500 | ||||||
chr5:74686524
|
C | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(190): Show | 229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.299+965C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686524 | ||||||
chr5:74686550
|
C | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0329a0001c0001t0001g0330others(8): Show | 12 | HG00741.hp2 HG01106.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.299+991C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686550 | ||||||
chr5:74686682
|
C | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.299+1123C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686682 | ||||||
chr5:74686764
|
T | G | 1 | a0001c0001t0001g0049 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.299+1205T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686764 | ||||||
chr5:74686799
|
T | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.299+1240T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686799 | ||||||
chr5:74686802
|
A | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.299+1243A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686802 | ||||||
chr5:74686867
|
G | C | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(192): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.299+1308G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686867 | ||||||
chr5:74686870
|
T | C | 45 | a0001c0001t0001g0050a0001c0001t0001g0215a0003c0003t0001g0005others(42): Show | 57 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.299+1311T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686870 | ||||||
chr5:74686964
|
G | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(190): Show | 229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.299+1405G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686964 | ||||||
chr5:74687014
|
C | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0219 | 3 | HG01891.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299+1455C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74687014 | ||||||
chr5:74687140
|
T | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(203): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.299+1581T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74687140 | ||||||
chr5:74687224
|
A | G | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(192): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.299+1665A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74687224 | ||||||
chr5:74687301
|
C | T | 1 | a0002c0002t0001g0328 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.299+1742C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74687301 | ||||||
chr5:74687907
|
G | T | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.300-1421G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74687907 | ||||||
chr5:74688042
|
T | G | 1 | a0010c0008t0001g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.300-1286T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688042 | ||||||
chr5:74688102
|
T | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0052a0001c0001t0001g0053others(5): Show | 11 | HG00642.hp1 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.300-1226T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688102 | ||||||
chr5:74688200
|
T | C | 1 | a0002c0002t0002g0028 | 2 | NA19074.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.300-1128T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688200 | ||||||
chr5:74688249
|
A | AT | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(192): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.300-1077dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 74688249 | |||||
chr5:74688328
|
A | C | 1 | a0001c0001t0002g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.300-1000A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688328 | ||||||
chr5:74688333
|
G | C | 1 | a0001c0001t0002g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.300-995G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688333 | ||||||
chr5:74688336
|
C | CT | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(185): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.300-979dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 74688336 | |||||
chr5:74688336
|
C | CTTTTTTT others(105): Show |
2 | a0001c0001t0001g0027a0001c0001t0001g0219 | 3 | HG01891.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.300-985_300-984ins others(112): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 74688336 | |||||
chr5:74688353
|
A | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 5 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-975A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688353 | ||||||
chr5:74688363
|
G | A | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(192): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.300-965G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688363 | ||||||
chr5:74688412
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.300-916G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688412 | ||||||
chr5:74688421
|
A | G | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(192): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.300-907A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688421 | ||||||
chr5:74688439
|
G | A | 206 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(203): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.300-889G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688439 | ||||||
chr5:74688589
|
C | T | 1 | a0003c0003t0001g0217 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.300-739C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688589 | ||||||
chr5:74688635
|
A | G | 92 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(89): Show | 103 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.300-693A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688635 | ||||||
chr5:74688785
|
C | T | 90 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(87): Show | 101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.300-543C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688785 | ||||||
chr5:74688818
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.300-510G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688818 | ||||||
chr5:74688897
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.300-431T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688897 | ||||||
chr5:74689052
|
C | CA | 90 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(87): Show | 101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.300-276_300-275ins others(1): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74689052 | ||||||
chr5:74689061
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.300-267A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74689061 | ||||||
chr5:74689088
|
A | G | 90 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(87): Show | 101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.300-240A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74689088 | ||||||
chr5:74689127
|
C | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.300-201C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74689127 | ||||||
chr5:74689282
|
T | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 6 | HG00140.hp2 HG00639.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.300-46T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74689282 | ||||||
chr5:74689296
|
C | T | 90 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(87): Show | 101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.300-32C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74689296 | ||||||
chr5:74689532
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054 | 6 | HG02145.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.445+59T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74689532 | ||||||
chr5:74689709
|
T | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(281): Show | 331 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.445+236T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74689709 | ||||||
chr5:74689753
|
A | C | 80 | a0002c0002t0001g0010a0002c0002t0001g0033a0002c0002t0001g0034others(77): Show | 90 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.445+280A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74689753 | ||||||
chr5:74689839
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.445+366T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74689839 | ||||||
chr5:74689972
|
T | G | 1 | a0002c0002t0001g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445+499T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74689972 | ||||||
chr5:74690010
|
CT | C | 285 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(282): Show | 332 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.445+542delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690010 | |||||
chr5:74690040
|
G | C | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445+567G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690040 | ||||||
chr5:74690085
|
A | G | 90 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(87): Show | 101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.445+612A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690085 | ||||||
chr5:74690175
|
T | C | 1 | a0010c0008t0001g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.445+702T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690175 | ||||||
chr5:74690317
|
A | G | 2 | a0001c0001t0001g0170a0003c0003t0002g0216 | 2 | HG00323.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.445+844A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690317 | ||||||
chr5:74690364
|
T | C | 90 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(87): Show | 101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.445+891T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690364 | ||||||
chr5:74690375
|
C | T | 90 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(87): Show | 101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.445+902C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690375 | ||||||
chr5:74690381
|
G | A | 90 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(87): Show | 101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.445+908G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690381 | ||||||
chr5:74690471
|
GA | G | 79 | a0002c0002t0001g0010a0002c0002t0001g0033a0002c0002t0001g0034others(76): Show | 89 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.445+1001delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690471 | |||||
chr5:74690478
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.445+1005C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690478 | ||||||
chr5:74690602
|
C | T | 92 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(89): Show | 103 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.445+1129C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690602 | ||||||
chr5:74690603
|
A | G | 92 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(89): Show | 103 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.445+1130A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690603 | ||||||
chr5:74690629
|
G | C | 1 | a0002c0002t0001g0260 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.445+1156G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690629 | ||||||
chr5:74690649
|
CAAAA | C | 18 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0069others(15): Show | 19 | HG01106.hp2 HG02015.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.445+1223_445+1226d others(6): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAA | C | 13 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(10): Show | 14 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.445+1222_445+1226d others(7): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0070 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.445+1217_445+1226d others(12): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 6 | HG02055.hp2 NA18982.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.445+1216_445+1226d others(13): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0056a0001c0001t0002g0074 | 2 | HG03098.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.445+1215_445+1226d others(14): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0001g0007a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 7 | HG00642.hp1 HG00673.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.445+1214_445+1226d others(15): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0001g0058a0001c0001t0001g0078 | 2 | HG01257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.445+1213_445+1226d others(16): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.445+1210_445+1226d others(19): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG01109.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.445+1208_445+1226d others(21): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(13): Show |
C | 6 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 9 | HG02145.hp2 HG02602.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+1207_445+1226d others(22): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(14): Show |
C | 1 | a0001c0001t0001g0258 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.445+1206_445+1226d others(23): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(17): Show |
C | 2 | a0001c0001t0001g0080a0010c0008t0001g0051 | 2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.445+1203_445+1226d others(26): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(18): Show |
C | 50 | a0001c0001t0001g0015a0001c0001t0001g0081a0001c0001t0001g0082others(47): Show | 63 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.445+1202_445+1226d others(27): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(19): Show |
C | 105 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0013others(102): Show | 121 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.445+1201_445+1226d others(28): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(20): Show |
C | 92 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(89): Show | 103 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.445+1200_445+1226d others(29): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(21): Show |
C | 8 | a0001c0001t0001g0044a0002c0002t0001g0322a0002c0002t0001g0323others(5): Show | 8 | HG00639.hp1 HG02895.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.445+1199_445+1226d others(30): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(23): Show |
C | 1 | a0001c0001t0001g0259 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.445+1197_445+1226d others(32): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690649
|
CAAAAAAA others(28): Show |
C | 2 | a0001c0001t0001g0027a0001c0001t0001g0219 | 3 | HG01891.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.445+1192_445+1226d others(37): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | |||||
chr5:74690698
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.445+1225A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690698 | ||||||
chr5:74690781
|
G | C | 1 | a0001c0001t0001g0222 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.445+1308G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690781 | ||||||
chr5:74690805
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445+1332T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690805 | ||||||
chr5:74690823
|
A | G | 181 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0012others(178): Show | 204 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.445+1350A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690823 | ||||||
chr5:74690928
|
T | C | 1 | a0010c0008t0001g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.445+1455T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690928 | ||||||
chr5:74690969
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.445+1496C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690969 | ||||||
chr5:74691001
|
T | C | 81 | a0001c0001t0001g0177a0002c0002t0001g0010a0002c0002t0001g0033others(78): Show | 91 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.445+1528T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691001 | ||||||
chr5:74691136
|
G | A | 1 | a0008c0009t0001g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.445+1663G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691136 | ||||||
chr5:74691223
|
C | T | 118 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0013others(115): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.445+1750C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691223 | ||||||
chr5:74691310
|
C | T | 81 | a0001c0001t0001g0177a0002c0002t0001g0010a0002c0002t0001g0033others(78): Show | 91 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.445+1837C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691310 | ||||||
chr5:74691529
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0159 | 6 | HG00408.hp2 HG00597.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.445+2056G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691529 | ||||||
chr5:74691665
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.446-1974G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691665 | ||||||
chr5:74691721
|
A | G | 92 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(89): Show | 103 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.446-1918A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691721 | ||||||
chr5:74691783
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.446-1856A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691783 | ||||||
chr5:74691817
|
C | G | 1 | a0003c0003t0001g0211 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.446-1822C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691817 | ||||||
chr5:74691950
|
A | G | 148 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0027others(145): Show | 178 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.446-1689A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691950 | ||||||
chr5:74691972
|
A | T | 2 | a0002c0002t0001g0038a0002c0002t0001g0321 | 3 | NA18975.hp2 NA18988.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.446-1667A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691972 | ||||||
chr5:74691973
|
GA | G | 6 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044others(3): Show | 6 | HG01109.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.446-1662delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74691973 | |||||
chr5:74692082
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0219 | 3 | HG01891.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.446-1557G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692082 | ||||||
chr5:74692323
|
C | T | 3 | a0005c0006t0001g0042a0005c0006t0001g0043a0005c0006t0001g0045 | 3 | HG01109.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.446-1316C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692323 | ||||||
chr5:74692334
|
C | CA | 20 | a0001c0001t0001g0053a0001c0001t0001g0059a0001c0001t0001g0069others(17): Show | 25 | HG01258.hp1 HG01884.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.446-1287dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74692334 | |||||
chr5:74692334
|
CA | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(9): Show | 13 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.446-1287delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74692334 | |||||
chr5:74692667
|
T | C | 10 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.446-972T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692667 | ||||||
chr5:74692721
|
G | A | 81 | a0001c0001t0001g0177a0002c0002t0001g0010a0002c0002t0001g0033others(78): Show | 91 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.446-918G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692721 | ||||||
chr5:74692863
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.446-776C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692863 | ||||||
chr5:74692911
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.446-728G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692911 | ||||||
chr5:74692990
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.446-649T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692990 | ||||||
chr5:74693013
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.446-626A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74693013 | ||||||
chr5:74693194
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.446-445G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74693194 | ||||||
chr5:74693302
|
A | G | 92 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(89): Show | 103 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.446-337A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74693302 | ||||||
chr5:74693472
|
C | T | 286 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(283): Show | 333 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.446-167C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74693472 | ||||||
chr5:74693731
|
C | T | 5 | a0002c0002t0001g0037a0002c0002t0001g0317a0002c0002t0001g0318others(2): Show | 6 | HG02895.hp2 HG02965.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.511+27C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693731 | ||||||
chr5:74693752
|
T | C | 2 | a0002c0002t0001g0265a0002c0002t0001g0328 | 2 | NA18972.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.511+48T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693752 | ||||||
chr5:74693855
|
T | G | 1 | a0002c0002t0001g0033 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.511+151T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693855 | ||||||
chr5:74693857
|
C | T | 1 | a0002c0002t0001g0033 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.511+153C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693857 | ||||||
chr5:74693859
|
A | C | 1 | a0002c0002t0001g0033 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.511+155A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693859 | ||||||
chr5:74693876
|
G | A | 3 | a0001c0001t0001g0329a0001c0001t0001g0331a0001c0001t0001g0336 | 3 | HG02559.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.511+172G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693876 | ||||||
chr5:74693929
|
G | A | 1 | a0002c0002t0001g0266 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.511+225G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693929 | ||||||
chr5:74693968
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.511+264G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693968 | ||||||
chr5:74693980
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0219 | 3 | HG01891.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.511+276G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693980 | ||||||
chr5:74694069
|
G | C | 80 | a0001c0001t0001g0177a0002c0002t0001g0010a0002c0002t0001g0033others(77): Show | 90 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.511+365G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694069 | ||||||
chr5:74694069
|
G | T | 1 | a0002c0002t0001g0316 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.511+365G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694069 | ||||||
chr5:74694105
|
G | A | 44 | a0003c0003t0001g0005a0003c0003t0001g0009a0003c0003t0001g0024others(41): Show | 56 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.511+401G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694105 | ||||||
chr5:74694187
|
A | G | 92 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(89): Show | 103 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.511+483A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694187 | ||||||
chr5:74694694
|
G | A | 3 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269 | 3 | HG01243.hp2 HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.511+990G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694694 | ||||||
chr5:74694733
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.511+1029G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694733 | ||||||
chr5:74694752
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.511+1048G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694752 | ||||||
chr5:74694810
|
C | CA | 82 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(79): Show | 92 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.511+1116dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr5 | 74694810 | |||||
chr5:74694824
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511+1120G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694824 | ||||||
chr5:74694839
|
G | C | 10 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.511+1135G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694839 | ||||||
chr5:74694959
|
A | G | 169 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(166): Show | 202 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.511+1255A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694959 | ||||||
chr5:74695050
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.511+1346C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695050 | ||||||
chr5:74695180
|
G | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.511+1476G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695180 | ||||||
chr5:74695201
|
C | CT | 32 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0047others(29): Show | 33 | HG00733.hp1 HG01243.hp1 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.512-1472dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr5 | 74695201 | |||||
chr5:74695201
|
CT | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0075a0001c0001t0001g0076others(11): Show | 16 | HG00673.hp2 HG01257.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.512-1472delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr5 | 74695201 | |||||
chr5:74695234
|
T | C | 85 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(82): Show | 98 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.512-1459T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695234 | ||||||
chr5:74695243
|
G | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.512-1450G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695243 | ||||||
chr5:74695360
|
C | T | 115 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0013others(112): Show | 129 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.512-1333C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695360 | ||||||
chr5:74695399
|
T | G | 1 | a0001c0001t0001g0238 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.512-1294T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695399 | ||||||
chr5:74695418
|
T | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054 | 6 | HG02145.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.512-1275T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695418 | ||||||
chr5:74695483
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.512-1210G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695483 | ||||||
chr5:74695579
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.512-1114G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695579 | ||||||
chr5:74695583
|
G | C | 340 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(337): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.512-1110G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695583 | ||||||
chr5:74695814
|
C | A | 2 | a0002c0002t0001g0317a0002c0002t0001g0318 | 2 | HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.512-879C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695814 | ||||||
chr5:74695839
|
T | TA | 191 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0013others(188): Show | 215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.512-837dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr5 | 74695839 | |||||
chr5:74695898
|
G | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.512-795G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695898 | ||||||
chr5:74695973
|
T | C | 1 | a0003c0003t0001g0186 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.512-720T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695973 | ||||||
chr5:74696204
|
A | C | 1 | a0001c0001t0001g0246 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.512-489A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74696204 | ||||||
chr5:74696387
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.512-306T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74696387 | ||||||
chr5:74696574
|
A | G | 1 | a0002c0002t0001g0036 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.512-119A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74696574 | ||||||
chr5:74696581
|
T | G | 168 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0013others(165): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.512-112T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74696581 | ||||||
chr5:74696784
|
G | A | 281 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(278): Show | 325 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.558+45G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 4/13 | chr5 | 74696784 | ||||||
chr5:74696978
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.559-18A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 4/13 | chr5 | 74696978 | ||||||
chr5:74697387
|
C | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0067a0001c0001t0001g0068others(5): Show | 9 | HG04184.hp2 NA18948.hp1 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+281C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697387 | ||||||
chr5:74697454
|
G | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 12 | HG00673.hp2 HG01257.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.669+348G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697454 | ||||||
chr5:74697483
|
T | C | 1 | a0010c0008t0001g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+377T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697483 | ||||||
chr5:74697505
|
C | T | 1 | a0002c0002t0001g0261 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.669+399C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697505 | ||||||
chr5:74697594
|
C | T | 1 | a0002c0002t0001g0308 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.669+488C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697594 | ||||||
chr5:74697595
|
G | A | 43 | a0003c0003t0001g0005a0003c0003t0001g0009a0003c0003t0001g0024others(40): Show | 55 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.669+489G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697595 | ||||||
chr5:74697727
|
C | CA | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(188): Show | 227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.669+640dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74697727 | |||||
chr5:74697727
|
C | CAA | 19 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0041others(16): Show | 20 | HG00673.hp1 HG02055.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.669+639_669+640dup others(2): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74697727 | |||||
chr5:74697727
|
CA | C | 71 | a0002c0002t0001g0010a0002c0002t0001g0034a0002c0002t0001g0035others(68): Show | 80 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.669+640delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74697727 | |||||
chr5:74697843
|
G | A | 1 | a0003c0003t0002g0188 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.669+737G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697843 | ||||||
chr5:74697868
|
T | G | 10 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+762T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697868 | ||||||
chr5:74697953
|
T | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0058 | 2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.669+847T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697953 | ||||||
chr5:74697975
|
C | T | 1 | a0010c0008t0001g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+869C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697975 | ||||||
chr5:74698046
|
A | C | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(280): Show | 327 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.669+940A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698046 | ||||||
chr5:74698055
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054 | 6 | HG02145.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+949A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698055 | ||||||
chr5:74698108
|
G | A | 44 | a0002c0002t0001g0010a0002c0002t0001g0033a0002c0002t0001g0034others(41): Show | 50 | HG00735.hp2 HG01081.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.669+1002G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698108 | ||||||
chr5:74698139
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.669+1033G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698139 | ||||||
chr5:74698146
|
C | T | 3 | a0002c0002t0001g0037a0002c0002t0001g0319a0002c0002t0001g0320 | 4 | HG02895.hp2 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+1040C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698146 | ||||||
chr5:74698178
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.669+1072A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698178 | ||||||
chr5:74698218
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.669+1112C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698218 | ||||||
chr5:74698239
|
A | G | 54 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(51): Show | 61 | HG00733.hp1 HG00735.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.669+1133A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698239 | ||||||
chr5:74698393
|
A | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+1287A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698393 | ||||||
chr5:74698395
|
TA | T | 20 | a0002c0002t0001g0010a0002c0002t0001g0033a0002c0002t0001g0036others(17): Show | 25 | HG01081.hp2 HG01167.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.669+1290delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698395 | ||||||
chr5:74698396
|
A | AT | 3 | a0003c0003t0001g0005a0003c0003t0001g0026a0003c0003t0002g0216 | 7 | HG00280.hp2 HG00738.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.669+1299dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74698396 | |||||
chr5:74698396
|
A | T | 70 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0040others(67): Show | 76 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.669+1290A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698396 | ||||||
chr5:74698396
|
AT | A | 23 | a0002c0002t0001g0034a0002c0002t0001g0260a0002c0002t0001g0265others(20): Show | 24 | HG00735.hp2 HG01243.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.669+1299delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74698396 | |||||
chr5:74698399
|
T | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0243a0010c0008t0001g0051 | 3 | HG02015.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.669+1293T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698399 | ||||||
chr5:74698400
|
T | A | 2 | a0002c0002t0001g0267a0002c0002t0001g0274 | 2 | HG01243.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.669+1294T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698400 | ||||||
chr5:74698431
|
C | T | 3 | a0002c0002t0001g0284a0002c0002t0001g0290a0002c0002t0001g0291 | 3 | HG01884.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.669+1325C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698431 | ||||||
chr5:74698436
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.669+1330G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698436 | ||||||
chr5:74698454
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.669+1348C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698454 | ||||||
chr5:74698468
|
T | A | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.669+1362T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698468 | ||||||
chr5:74698477
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.669+1371C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698477 | ||||||
chr5:74698485
|
G | A | 44 | a0002c0002t0001g0010a0002c0002t0001g0033a0002c0002t0001g0034others(41): Show | 50 | HG00735.hp2 HG01081.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.669+1379G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698485 | ||||||
chr5:74698508
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 5 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+1402C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698508 | ||||||
chr5:74698641
|
C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0075a0001c0001t0001g0076others(6): Show | 11 | HG00673.hp2 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+1535C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698641 | ||||||
chr5:74698868
|
T | G | 11 | a0001c0001t0001g0014a0001c0001t0001g0067a0001c0001t0001g0068others(8): Show | 12 | HG00438.hp1 HG03239.hp2 HG04184.hp2 others(9): Show |
intron_variant | MODIFIER | c.669+1762T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698868 | ||||||
chr5:74699270
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.669+2164A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699270 | ||||||
chr5:74699271
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.669+2165C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699271 | ||||||
chr5:74699289
|
T | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0116 | 2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.669+2183T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699289 | ||||||
chr5:74699317
|
A | G | 1 | a0001c0001t0001g0334 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.669+2211A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699317 | ||||||
chr5:74699357
|
C | G | 1 | a0002c0002t0001g0322 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.669+2251C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699357 | ||||||
chr5:74699369
|
AGTTCAAG others(725): Show |
A | 1 | a0001c0001t0001g0236 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.669+2272_669+3003d others(2): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74699369 | |||||
chr5:74699400
|
G | C | 1 | a0003c0003t0001g0211 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.669+2294G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699400 | ||||||
chr5:74699417
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.669+2311G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699417 | ||||||
chr5:74699418
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.669+2312G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699418 | ||||||
chr5:74699482
|
TCAGGCTG others(1426): Show |
T | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.669+2404_669+3836d others(2): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74699482 | |||||
chr5:74699516
|
T | C | 12 | a0001c0001t0001g0039a0001c0001t0001g0227a0001c0001t0001g0245others(9): Show | 13 | HG00741.hp2 HG01106.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.669+2410T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699516 | ||||||
chr5:74699552
|
G | A | 12 | a0001c0001t0001g0039a0001c0001t0001g0227a0001c0001t0001g0245others(9): Show | 13 | HG00741.hp2 HG01106.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.669+2446G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699552 | ||||||
chr5:74699794
|
A | G | 34 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0110others(31): Show | 44 | HG00408.hp2 HG00597.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+2688A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699794 | ||||||
chr5:74699947
|
C | CT | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(279): Show | 328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.669+2849dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74699947 | |||||
chr5:74700001
|
C | CT | 10 | a0001c0001t0001g0047a0001c0001t0001g0072a0001c0001t0001g0073others(7): Show | 10 | HG00140.hp1 HG00735.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.669+2920dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74700001 | |||||
chr5:74700001
|
CT | C | 22 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0059others(19): Show | 26 | HG00408.hp2 HG00558.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.669+2920delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74700001 | |||||
chr5:74700001
|
CTT | C | 198 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.669+2919_669+2920d others(4): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74700001 | |||||
chr5:74700001
|
CTTT | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(8): Show | 14 | HG00323.hp1 HG00558.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.669+2918_669+2920d others(5): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74700001 | |||||
chr5:74700001
|
CTTTT | C | 10 | a0001c0001t0001g0039a0001c0001t0001g0227a0001c0001t0001g0245others(7): Show | 11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+2917_669+2920d others(6): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74700001 | |||||
chr5:74700001
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0096 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.669+2908_669+2920d others(15): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74700001 | |||||
chr5:74700070
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.669+2964A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700070 | ||||||
chr5:74700109
|
C | T | 1 | a0002c0002t0001g0288 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.669+3003C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700109 | ||||||
chr5:74700146
|
A | G | 1 | a0002c0002t0001g0322 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.669+3040A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700146 | ||||||
chr5:74700163
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.669+3057C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700163 | ||||||
chr5:74700164
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.669+3058A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700164 | ||||||
chr5:74700165
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.669+3059C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700165 | ||||||
chr5:74700285
|
G | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 7 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.669+3179G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700285 | ||||||
chr5:74700582
|
G | C | 232 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(229): Show | 264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.669+3476G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700582 | ||||||
chr5:74700723
|
T | C | 3 | a0006c0007t0001g0055a0006c0007t0001g0057a0006c0007t0001g0178 | 3 | HG00642.hp1 HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.669+3617T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700723 | ||||||
chr5:74700729
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0234 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.669+3623C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700729 | ||||||
chr5:74700771
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.669+3665G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700771 | ||||||
chr5:74700818
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.669+3712C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700818 | ||||||
chr5:74700999
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(180): Show | 211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.669+3893T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700999 | ||||||
chr5:74701050
|
A | AT | 10 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0048others(7): Show | 14 | HG00733.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.669+3958dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74701050 | |||||
chr5:74701050
|
AT | A | 8 | a0001c0001t0001g0121a0001c0001t0001g0148a0001c0001t0001g0160others(5): Show | 8 | HG01069.hp2 HG01169.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.669+3958delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74701050 | |||||
chr5:74701108
|
C | T | 2 | a0003c0003t0001g0199a0003c0003t0001g0214 | 2 | HG00423.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.669+4002C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701108 | ||||||
chr5:74701120
|
C | T | 10 | a0001c0001t0001g0039a0001c0001t0001g0227a0001c0001t0001g0245others(7): Show | 11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+4014C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701120 | ||||||
chr5:74701500
|
A | T | 1 | a0001c0001t0001g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.670-3719A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701500 | ||||||
chr5:74701699
|
A | T | 34 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0041others(31): Show | 36 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.670-3520A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701699 | ||||||
chr5:74701747
|
A | G | 1 | a0003c0003t0001g0209 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.670-3472A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701747 | ||||||
chr5:74701793
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.670-3426C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701793 | ||||||
chr5:74701904
|
G | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0097 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.670-3315G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701904 | ||||||
chr5:74701939
|
C | T | 2 | a0002c0002t0001g0284a0002c0002t0001g0291 | 2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.670-3280C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701939 | ||||||
chr5:74702032
|
C | A | 1 | a0003c0003t0001g0193 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.670-3187C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702032 | ||||||
chr5:74702061
|
C | A | 20 | a0001c0001t0001g0052a0001c0001t0001g0072a0001c0001t0001g0073others(17): Show | 25 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.670-3158C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702061 | ||||||
chr5:74702063
|
T | G | 3 | a0001c0001t0001g0056a0001c0001t0001g0069a0005c0006t0001g0045 | 3 | HG03041.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.670-3156T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702063 | ||||||
chr5:74702067
|
C | CT | 14 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0103others(11): Show | 14 | HG01109.hp1 HG01175.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-3123dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74702067 | |||||
chr5:74702067
|
CT | C | 16 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0077others(13): Show | 17 | HG00558.hp1 HG01975.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.670-3123delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74702067 | |||||
chr5:74702067
|
CTT | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(60): Show | 73 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.670-3124_670-3123d others(4): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74702067 | |||||
chr5:74702067
|
CTTT | C | 180 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(177): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.670-3125_670-3123d others(5): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74702067 | |||||
chr5:74702067
|
CTTTT | C | 24 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0039others(21): Show | 27 | HG00597.hp1 HG00639.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.670-3126_670-3123d others(6): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74702067 | |||||
chr5:74702067
|
CTTTTT | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0048others(2): Show | 6 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-3127_670-3123d others(7): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74702067 | |||||
chr5:74702109
|
C | T | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.670-3110C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702109 | ||||||
chr5:74702117
|
C | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.670-3102C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702117 | ||||||
chr5:74702148
|
G | A | 216 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(213): Show | 246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.670-3071G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702148 | ||||||
chr5:74702239
|
T | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.670-2980T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702239 | ||||||
chr5:74702241
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 7 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-2978G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702241 | ||||||
chr5:74702305
|
C | T | 1 | a0003c0003t0002g0207 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.670-2914C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702305 | ||||||
chr5:74702325
|
G | A | 33 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0050others(30): Show | 34 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.670-2894G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702325 | ||||||
chr5:74702369
|
C | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0107others(4): Show | 7 | HG00673.hp2 NA18940.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-2850C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702369 | ||||||
chr5:74702670
|
G | T | 1 | a0001c0010t0001g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.670-2549G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702670 | ||||||
chr5:74702726
|
C | T | 1 | a0002c0002t0001g0288 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.670-2493C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702726 | ||||||
chr5:74702883
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.670-2336G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702883 | ||||||
chr5:74702896
|
G | T | 34 | a0001c0001t0001g0056a0001c0001t0001g0069a0001c0001t0002g0074others(31): Show | 41 | HG00673.hp1 HG00741.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.670-2323G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702896 | ||||||
chr5:74703044
|
C | G | 1 | a0001c0001t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.670-2175C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703044 | ||||||
chr5:74703055
|
C | T | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.670-2164C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703055 | ||||||
chr5:74703077
|
T | G | 1 | a0001c0001t0001g0027 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.670-2142T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703077 | ||||||
chr5:74703149
|
C | T | 30 | a0001c0001t0002g0074a0001c0001t0002g0095a0001c0001t0002g0147others(27): Show | 37 | HG00673.hp1 HG00741.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.670-2070C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703149 | ||||||
chr5:74703214
|
A | G | 34 | a0001c0001t0001g0056a0001c0001t0001g0069a0001c0001t0002g0074others(31): Show | 41 | HG00673.hp1 HG00741.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.670-2005A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703214 | ||||||
chr5:74703235
|
G | T | 1 | a0001c0010t0001g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.670-1984G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703235 | ||||||
chr5:74703380
|
T | C | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(294): Show | 344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.670-1839T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703380 | ||||||
chr5:74703401
|
C | T | 3 | a0001c0001t0001g0156a0002c0002t0001g0299a0003c0003t0002g0216 | 3 | HG01175.hp1 HG01346.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.670-1818C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703401 | ||||||
chr5:74703535
|
G | C | 2 | a0002c0002t0001g0261a0002c0002t0001g0309 | 2 | HG00621.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.670-1684G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703535 | ||||||
chr5:74703606
|
T | C | 2 | a0002c0002t0001g0268a0002c0002t0001g0322 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.670-1613T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703606 | ||||||
chr5:74703607
|
A | G | 66 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0017others(63): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.670-1612A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703607 | ||||||
chr5:74703614
|
C | T | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.670-1605C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703614 | ||||||
chr5:74703616
|
A | T | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.670-1603A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703616 | ||||||
chr5:74703807
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0069a0005c0006t0001g0045 | 3 | HG03041.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.670-1412C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703807 | ||||||
chr5:74703817
|
G | A | 1 | a0001c0001t0001g0027 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.670-1402G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703817 | ||||||
chr5:74703957
|
A | G | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.670-1262A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703957 | ||||||
chr5:74703969
|
G | A | 10 | a0001c0001t0001g0039a0001c0001t0001g0227a0001c0001t0001g0245others(7): Show | 11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.670-1250G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703969 | ||||||
chr5:74703975
|
G | A | 2 | a0002c0002t0001g0265a0002c0002t0001g0328 | 2 | NA18972.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.670-1244G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703975 | ||||||
chr5:74704006
|
G | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.670-1213G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704006 | ||||||
chr5:74704013
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0162 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.670-1206C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704013 | ||||||
chr5:74704042
|
A | G | 10 | a0001c0001t0001g0039a0001c0001t0001g0227a0001c0001t0001g0245others(7): Show | 11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.670-1177A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704042 | ||||||
chr5:74704259
|
C | T | 187 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(184): Show | 220 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.670-960C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704259 | ||||||
chr5:74704260
|
C | A | 1 | a0001c0001t0001g0027 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.670-959C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704260 | ||||||
chr5:74704305
|
C | T | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.670-914C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704305 | ||||||
chr5:74704370
|
G | T | 200 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(197): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.670-849G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704370 | ||||||
chr5:74704443
|
A | G | 2 | a0001c0001t0001g0021a0007c0013t0001g0021 | 2 | HG00642.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.670-776A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704443 | ||||||
chr5:74704529
|
C | T | 6 | a0001c0001t0001g0332a0001c0001t0001g0337a0002c0002t0001g0037others(3): Show | 7 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-690C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704529 | ||||||
chr5:74704574
|
G | A | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(294): Show | 344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.670-645G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704574 | ||||||
chr5:74704802
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.670-417T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704802 | ||||||
chr5:74704812
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.670-407C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704812 | ||||||
chr5:74704868
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.670-351G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704868 | ||||||
chr5:74704945
|
A | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.670-274A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704945 | ||||||
chr5:74705091
|
C | CA | 65 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0047others(62): Show | 72 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.670-107dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74705091 | |||||
chr5:74705091
|
CA | C | 198 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 234 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.670-107delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74705091 | |||||
chr5:74705091
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.670-118_670-107del others(12): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74705091 | |||||
chr5:74705535
|
A | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0133 | 2 | HG01074.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.771+215A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705535 | ||||||
chr5:74705540
|
A | G | 12 | a0001c0001t0001g0075a0001c0001t0001g0244a0001c0001t0001g0249others(9): Show | 12 | HG01928.hp2 HG01943.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.771+220A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705540 | ||||||
chr5:74705656
|
C | A | 6 | a0002c0002t0001g0034a0002c0002t0001g0270a0002c0002t0001g0274others(3): Show | 7 | HG01361.hp1 HG01496.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+336C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705656 | ||||||
chr5:74705757
|
A | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(8): Show | 14 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.771+437A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705757 | ||||||
chr5:74705792
|
T | C | 20 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0108others(17): Show | 22 | HG00597.hp1 HG00735.hp2 HG02148.hp1 others(19): Show |
intron_variant | MODIFIER | c.771+472T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705792 | ||||||
chr5:74705874
|
G | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.771+554G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705874 | ||||||
chr5:74705929
|
A | C | 1 | a0003c0003t0002g0200 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.771+609A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705929 | ||||||
chr5:74706152
|
G | A | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.771+832G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706152 | ||||||
chr5:74706351
|
G | C | 1 | a0001c0001t0001g0111 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.771+1031G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706351 | ||||||
chr5:74706416
|
T | C | 1 | a0002c0002t0001g0282 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.771+1096T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706416 | ||||||
chr5:74706443
|
C | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0117a0001c0001t0001g0243others(1): Show | 4 | HG00558.hp1 HG02015.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.771+1123C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706443 | ||||||
chr5:74706447
|
G | A | 3 | a0006c0007t0001g0055a0006c0007t0001g0057a0006c0007t0001g0178 | 3 | HG00642.hp1 HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.771+1127G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706447 | ||||||
chr5:74706472
|
G | A | 12 | a0001c0001t0001g0076a0001c0001t0001g0084a0001c0001t0001g0089others(9): Show | 12 | HG00673.hp2 HG02056.hp2 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.771+1152G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706472 | ||||||
chr5:74706473
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.771+1153C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706473 | ||||||
chr5:74706474
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.771+1154G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706474 | ||||||
chr5:74706489
|
G | C | 10 | a0001c0001t0001g0039a0001c0001t0001g0227a0001c0001t0001g0245others(7): Show | 11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.771+1169G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706489 | ||||||
chr5:74706506
|
G | A | 211 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(208): Show | 247 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.771+1186G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706506 | ||||||
chr5:74706569
|
G | A | 252 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(249): Show | 289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.771+1249G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706569 | ||||||
chr5:74706578
|
G | A | 10 | a0001c0001t0001g0039a0001c0001t0001g0227a0001c0001t0001g0245others(7): Show | 11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.771+1258G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706578 | ||||||
chr5:74706610
|
G | A | 1 | a0001c0001t0001g0027 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.771+1290G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706610 | ||||||
chr5:74706613
|
G | A | 52 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(49): Show | 55 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.771+1293G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706613 | ||||||
chr5:74706653
|
C | A | 1 | a0001c0001t0001g0027 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.771+1333C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706653 | ||||||
chr5:74706689
|
G | C | 42 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0041others(39): Show | 44 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.771+1369G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706689 | ||||||
chr5:74706732
|
C | T | 1 | a0003c0003t0001g0180 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.771+1412C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706732 | ||||||
chr5:74706791
|
G | A | 10 | a0001c0001t0001g0039a0001c0001t0001g0227a0001c0001t0001g0245others(7): Show | 11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.771+1471G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706791 | ||||||
chr5:74706832
|
G | A | 210 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(207): Show | 245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.771+1512G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706832 | ||||||
chr5:74706979
|
C | T | 42 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0041others(39): Show | 44 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.771+1659C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706979 | ||||||
chr5:74707106
|
C | T | 37 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0050others(34): Show | 38 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.771+1786C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707106 | ||||||
chr5:74707129
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.771+1809T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707129 | ||||||
chr5:74707131
|
C | T | 1 | a0003c0003t0002g0205 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.771+1811C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707131 | ||||||
chr5:74707133
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.771+1813C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707133 | ||||||
chr5:74707169
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.771+1849C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707169 | ||||||
chr5:74707171
|
C | G | 1 | a0001c0001t0001g0086 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.771+1851C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707171 | ||||||
chr5:74707175
|
C | T | 1 | a0002c0002t0001g0260 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.771+1855C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707175 | ||||||
chr5:74707276
|
C | A | 1 | a0002c0002t0001g0288 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.771+1956C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707276 | ||||||
chr5:74707306
|
A | C | 1 | a0001c0001t0001g0027 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.771+1986A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707306 | ||||||
chr5:74707360
|
C | T | 1 | a0003c0003t0001g0191 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.771+2040C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707360 | ||||||
chr5:74707439
|
G | A | 1 | a0002c0002t0001g0316 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.771+2119G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707439 | ||||||
chr5:74707454
|
T | C | 52 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(49): Show | 55 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.771+2134T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707454 | ||||||
chr5:74707754
|
A | C | 1 | a0001c0001t0001g0232 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.771+2434A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707754 | ||||||
chr5:74707822
|
CTGAAAG | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.771+2512_771+2517d others(8): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 74707822 | |||||
chr5:74707838
|
C | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0333a0002c0002t0001g0036others(2): Show | 6 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.771+2518C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707838 | ||||||
chr5:74707863
|
T | G | 3 | a0006c0007t0001g0055a0006c0007t0001g0057a0006c0007t0001g0178 | 3 | HG00642.hp1 HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.771+2543T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707863 | ||||||
chr5:74707966
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.771+2646G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707966 | ||||||
chr5:74708057
|
A | T | 5 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0115others(2): Show | 5 | HG00438.hp1 HG00735.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+2737A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708057 | ||||||
chr5:74708093
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.771+2773C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708093 | ||||||
chr5:74708201
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | NA18982.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.771+2881G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708201 | ||||||
chr5:74708325
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 7 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+3005G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708325 | ||||||
chr5:74708387
|
A | G | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(294): Show | 344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.771+3067A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708387 | ||||||
chr5:74708526
|
G | A | 22 | a0001c0001t0001g0052a0001c0001t0001g0072a0001c0001t0001g0073others(19): Show | 27 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.771+3206G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708526 | ||||||
chr5:74708532
|
G | T | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.771+3212G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708532 | ||||||
chr5:74708577
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.771+3257T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708577 | ||||||
chr5:74708626
|
T | G | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.771+3306T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708626 | ||||||
chr5:74708704
|
C | T | 1 | a0002c0002t0001g0281 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.771+3384C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708704 | ||||||
chr5:74708722
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.771+3402A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708722 | ||||||
chr5:74708734
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.771+3414A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708734 | ||||||
chr5:74708792
|
C | A | 1 | a0002c0002t0001g0288 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.771+3472C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708792 | ||||||
chr5:74708883
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.771+3563C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708883 | ||||||
chr5:74709153
|
C | T | 223 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(220): Show | 262 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.771+3833C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709153 | ||||||
chr5:74709190
|
T | C | 2 | a0001c0001t0001g0144a0003c0003t0001g0213 | 2 | NA18612.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.771+3870T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709190 | ||||||
chr5:74709328
|
C | CA | 5 | a0003c0003t0001g0198a0003c0003t0002g0025a0003c0003t0002g0181others(2): Show | 6 | NA18944.hp1 NA18986.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.771+4010dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 74709328 | |||||
chr5:74709367
|
A | T | 1 | a0001c0001t0001g0015 | 2 | NA18954.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.771+4047A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709367 | ||||||
chr5:74709481
|
T | G | 3 | a0001c0001t0001g0056a0001c0001t0001g0069a0005c0006t0001g0045 | 3 | HG03041.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.772-4025T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709481 | ||||||
chr5:74709533
|
G | T | 1 | a0001c0001t0001g0246 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.772-3973G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709533 | ||||||
chr5:74709554
|
A | G | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.772-3952A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709554 | ||||||
chr5:74709654
|
C | T | 23 | a0001c0001t0001g0052a0001c0001t0001g0072a0001c0001t0001g0073others(20): Show | 28 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.772-3852C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709654 | ||||||
chr5:74709715
|
T | A | 2 | a0003c0003t0002g0184a0003c0003t0002g0185 | 2 | NA18965.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.772-3791T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709715 | ||||||
chr5:74709757
|
A | G | 4 | a0001c0001t0001g0244a0001c0001t0001g0249a0001c0001t0001g0254others(1): Show | 4 | NA18972.hp1 NA18975.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.772-3749A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709757 | ||||||
chr5:74709841
|
C | T | 1 | a0003c0003t0002g0204 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.772-3665C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709841 | ||||||
chr5:74709862
|
G | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0097 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.772-3644G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709862 | ||||||
chr5:74709936
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.772-3570A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709936 | ||||||
chr5:74709945
|
G | A | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.772-3561G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709945 | ||||||
chr5:74709967
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.772-3539G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709967 | ||||||
chr5:74709987
|
AAGAGAAT others(3): Show |
A | 21 | a0001c0001t0001g0052a0001c0001t0001g0073a0001c0001t0001g0077others(18): Show | 26 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.772-3515_772-3506d others(12): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 74709987 | |||||
chr5:74710034
|
C | G | 1 | a0001c0001t0001g0232 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.772-3472C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710034 | ||||||
chr5:74710038
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 7 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.772-3468A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710038 | ||||||
chr5:74710117
|
G | A | 1 | a0001c0010t0001g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.772-3389G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710117 | ||||||
chr5:74710122
|
C | G | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(124): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.772-3384C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710122 | ||||||
chr5:74710136
|
C | T | 20 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0108others(17): Show | 22 | HG00597.hp1 HG00735.hp2 HG02148.hp1 others(19): Show |
intron_variant | MODIFIER | c.772-3370C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710136 | ||||||
chr5:74710240
|
C | G | 1 | a0001c0001t0001g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.772-3266C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710240 | ||||||
chr5:74710282
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(113): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.772-3224A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710282 | ||||||
chr5:74710298
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(61): Show | 77 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.772-3208A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710298 | ||||||
chr5:74710319
|
C | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(124): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.772-3187C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710319 | ||||||
chr5:74710341
|
G | T | 39 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0041others(36): Show | 41 | HG00140.hp2 HG00280.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.772-3165G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710341 | ||||||
chr5:74710359
|
TC | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(40): Show | 51 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.772-3144delC | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 74710359 | |||||
chr5:74710420
|
G | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(40): Show | 51 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.772-3086G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710420 | ||||||
chr5:74710518
|
T | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-2988T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710518 | ||||||
chr5:74710519
|
G | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-2987G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710519 | ||||||
chr5:74710524
|
T | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-2982T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710524 | ||||||
chr5:74710543
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.772-2963T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710543 | ||||||
chr5:74710636
|
C | T | 21 | a0001c0001t0001g0052a0001c0001t0001g0073a0001c0001t0001g0077others(18): Show | 26 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.772-2870C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710636 | ||||||
chr5:74710788
|
T | C | 32 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0058others(29): Show | 33 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.772-2718T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710788 | ||||||
chr5:74710794
|
C | G | 1 | a0003c0003t0001g0191 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.772-2712C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710794 | ||||||
chr5:74710860
|
C | G | 1 | a0001c0001t0001g0330 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.772-2646C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710860 | ||||||
chr5:74710967
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(113): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.772-2539A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710967 | ||||||
chr5:74711016
|
G | A | 1 | a0001c0001t0001g0027 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.772-2490G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711016 | ||||||
chr5:74711049
|
A | C | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.772-2457A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711049 | ||||||
chr5:74711051
|
T | C | 52 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(49): Show | 55 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.772-2455T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711051 | ||||||
chr5:74711070
|
C | T | 1 | a0006c0007t0001g0055 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.772-2436C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711070 | ||||||
chr5:74711108
|
C | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0077 | 2 | HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.772-2398C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711108 | ||||||
chr5:74711126
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0069a0005c0006t0001g0045 | 3 | HG03041.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.772-2380C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711126 | ||||||
chr5:74711151
|
G | C | 1 | a0002c0002t0001g0303 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.772-2355G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711151 | ||||||
chr5:74711273
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.772-2233C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711273 | ||||||
chr5:74711664
|
A | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(62): Show | 78 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.772-1842A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711664 | ||||||
chr5:74711692
|
A | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-1814A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711692 | ||||||
chr5:74711702
|
G | A | 2 | a0001c0001t0001g0230a0003c0003t0001g0189 | 2 | HG01975.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.772-1804G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711702 | ||||||
chr5:74711713
|
G | GAGCGATG others(33): Show |
3 | a0003c0003t0002g0025a0003c0003t0002g0181a0003c0003t0002g0206 | 4 | NA18944.hp1 NA18986.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.772-1793_772-1792i others(42): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711713 | ||||||
chr5:74711714
|
C | A | 3 | a0003c0003t0002g0025a0003c0003t0002g0181a0003c0003t0002g0206 | 4 | NA18944.hp1 NA18986.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.772-1792C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711714 | ||||||
chr5:74711728
|
A | T | 1 | a0002c0002t0001g0293 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.772-1778A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711728 | ||||||
chr5:74711739
|
A | G | 1 | a0001c0001t0001g0027 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.772-1767A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711739 | ||||||
chr5:74711750
|
T | G | 36 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0050others(33): Show | 37 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.772-1756T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711750 | ||||||
chr5:74711799
|
G | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-1707G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711799 | ||||||
chr5:74711964
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(61): Show | 77 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.772-1542G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711964 | ||||||
chr5:74711994
|
T | C | 1 | a0003c0003t0002g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.772-1512T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711994 | ||||||
chr5:74712175
|
A | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(126): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.772-1331A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712175 | ||||||
chr5:74712234
|
G | C | 1 | a0002c0002t0001g0267 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.772-1272G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712234 | ||||||
chr5:74712372
|
T | G | 1 | a0005c0006t0001g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.772-1134T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712372 | ||||||
chr5:74712433
|
T | TA | 61 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(58): Show | 74 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.772-1071dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 74712433 | |||||
chr5:74712435
|
AT | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0017others(47): Show | 55 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.772-1070delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712435 | ||||||
chr5:74712436
|
T | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0027others(77): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.772-1070T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712436 | ||||||
chr5:74712461
|
T | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(64): Show | 80 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.772-1045T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712461 | ||||||
chr5:74712585
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.772-921T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712585 | ||||||
chr5:74712586
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.772-920T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712586 | ||||||
chr5:74712588
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.772-918T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712588 | ||||||
chr5:74712601
|
T | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(114): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.772-905T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712601 | ||||||
chr5:74712691
|
C | T | 3 | a0001c0004t0001g0006a0001c0004t0001g0218a0002c0002t0001g0292 | 6 | HG01884.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.772-815C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712691 | ||||||
chr5:74712694
|
C | T | 2 | a0002c0002t0001g0272a0002c0002t0001g0280 | 2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.772-812C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712694 | ||||||
chr5:74712698
|
C | T | 117 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(114): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.772-808C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712698 | ||||||
chr5:74712849
|
C | T | 3 | a0001c0004t0001g0006a0001c0004t0001g0218a0002c0002t0001g0292 | 6 | HG01884.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.772-657C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712849 | ||||||
chr5:74712938
|
A | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(62): Show | 78 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.772-568A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712938 | ||||||
chr5:74713119
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(62): Show | 78 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.772-387G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74713119 | ||||||
chr5:74713196
|
G | A | 11 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(8): Show | 14 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.772-310G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74713196 | ||||||
chr5:74713254
|
C | A | 1 | a0001c0001t0001g0027 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.772-252C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74713254 | ||||||
chr5:74713374
|
T | G | 5 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0115others(2): Show | 5 | HG00438.hp1 HG00735.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-132T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74713374 | ||||||
chr5:74713467
|
C | T | 9 | a0001c0001t0001g0039a0001c0001t0001g0227a0001c0001t0001g0245others(6): Show | 10 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.772-39C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74713467 | ||||||
chr5:74713502
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0059others(5): Show | 10 | HG00639.hp2 HG01074.hp2 HG01169.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.772-4A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74713502 | ||||||
chr5:74713733
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.901+98G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74713733 | ||||||
chr5:74713944
|
G | T | 4 | a0001c0001t0001g0244a0001c0001t0001g0249a0001c0001t0001g0254others(1): Show | 4 | NA18972.hp1 NA18975.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.901+309G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74713944 | ||||||
chr5:74714027
|
G | C | 3 | a0001c0001t0001g0056a0001c0001t0001g0069a0005c0006t0001g0045 | 3 | HG03041.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.901+392G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714027 | ||||||
chr5:74714110
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.901+475T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714110 | ||||||
chr5:74714183
|
T | C | 1 | a0003c0003t0002g0210 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.901+548T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714183 | ||||||
chr5:74714277
|
C | G | 11 | a0001c0001t0001g0050a0001c0001t0001g0064a0001c0001t0001g0091others(8): Show | 11 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.901+642C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714277 | ||||||
chr5:74714625
|
T | C | 1 | a0003c0003t0002g0205 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.902-885T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714625 | ||||||
chr5:74714801
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.902-709G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714801 | ||||||
chr5:74714934
|
C | T | 3 | a0001c0004t0001g0006a0001c0004t0001g0218a0002c0002t0001g0292 | 6 | HG01884.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.902-576C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714934 | ||||||
chr5:74715108
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.902-402G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74715108 | ||||||
chr5:74715242
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.902-268A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74715242 | ||||||
chr5:74715459
|
CT | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(61): Show | 77 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.902-48delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 74715459 | |||||
chr5:74715716
|
T | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(71): Show | 90 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1082+26T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | chr5 | 74715716 | ||||||
chr5:74715716
|
T | TA | 7 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0047others(4): Show | 9 | HG00733.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1082+40dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 74715716 | |||||
chr5:74715991
|
T | G | 52 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(49): Show | 55 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1082+301T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | chr5 | 74715991 | ||||||
chr5:74716016
|
C | CA | 33 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0065others(30): Show | 35 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1082+351dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 74716016 | |||||
chr5:74716016
|
CA | C | 46 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0027others(43): Show | 58 | HG00741.hp1 HG01123.hp1 HG01175.hp1 others(55): Show |
intron_variant | MODIFIER | c.1082+351delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 74716016 | |||||
chr5:74716016
|
CAA | C | 16 | a0001c0001t0001g0039a0001c0001t0001g0056a0001c0001t0001g0069others(13): Show | 17 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.1082+350_1082+351d others(4): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 74716016 | |||||
chr5:74716016
|
CAAA | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(56): Show | 72 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1082+349_1082+351d others(5): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 74716016 | |||||
chr5:74716027
|
AAAAAAAA others(8): Show |
A | 4 | a0001c0001t0001g0017a0001c0001t0001g0083a0001c0001t0001g0104others(1): Show | 5 | HG01081.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1082+338_1082+352d others(17): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | chr5 | 74716027 | ||||||
chr5:74716040
|
AAT | A | 35 | a0001c0001t0001g0012a0001c0001t0001g0041a0001c0001t0001g0047others(32): Show | 36 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1082+351_1082+352d others(4): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | chr5 | 74716040 | ||||||
chr5:74716044
|
G | T | 1 | a0001c0001t0001g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1082+354G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | chr5 | 74716044 | ||||||
chr5:74716734
|
G | A | 1 | a0001c0001t0001g0027 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1169+61G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74716734 | ||||||
chr5:74716762
|
T | A | 4 | a0002c0002t0001g0268a0002c0002t0001g0269a0002c0002t0001g0322others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169+89T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74716762 | ||||||
chr5:74716915
|
C | T | 1 | a0003c0003t0001g0005 | 4 | HG00280.hp2 HG00738.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1169+242C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74716915 | ||||||
chr5:74716918
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1169+245G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74716918 | ||||||
chr5:74717017
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1169+344C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717017 | ||||||
chr5:74717066
|
T | A | 1 | a0005c0006t0001g0045 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1169+393T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717066 | ||||||
chr5:74717086
|
C | T | 1 | a0003c0003t0001g0195 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1169+413C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717086 | ||||||
chr5:74717246
|
G | A | 1 | a0002c0002t0001g0275 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1169+573G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717246 | ||||||
chr5:74717414
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 7 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1169+741C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717414 | ||||||
chr5:74717428
|
C | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(42): Show | 53 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1169+755C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717428 | ||||||
chr5:74717450
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1169+777G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717450 | ||||||
chr5:74717477
|
C | CAT | 53 | a0001c0001t0001g0015a0001c0001t0001g0029a0001c0001t0001g0031others(50): Show | 60 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1170-796_1170-795d others(4): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | |||||
chr5:74717477
|
C | CATAT | 24 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0041others(21): Show | 30 | HG01257.hp1 HG01258.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.1170-798_1170-795d others(6): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | |||||
chr5:74717477
|
C | CATATAT | 5 | a0001c0001t0001g0103a0001c0001t0001g0333a0002c0002t0001g0036others(2): Show | 6 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170-800_1170-795d others(8): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | |||||
chr5:74717477
|
C | CATATATA others(1): Show |
45 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(42): Show | 48 | HG00140.hp2 HG00280.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1170-802_1170-795d others(10): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | |||||
chr5:74717477
|
C | CATATATA others(3): Show |
2 | a0001c0001t0001g0177a0002c0002t0001g0267 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1170-804_1170-795d others(12): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | |||||
chr5:74717477
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0091 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1170-806_1170-795d others(14): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | |||||
chr5:74717477
|
CAT | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0053others(8): Show | 15 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1170-796_1170-795d others(4): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | |||||
chr5:74717670
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T | TA | 3 | a0001c0001t0001g0109a0001c0001t0001g0171a0002c0002t0001g0010 | 5 | HG02809.hp1 HG03041.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170-612dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717670 | |||||
chr5:74717714
|
G | A | 1 | a0002c0002t0001g0302 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1170-577G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717714 | ||||||
chr5:74717782
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1170-509C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717782 | ||||||
chr5:74717786
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A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(255): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1170-505A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717786 | ||||||
chr5:74718418
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T | C | 1 | a0001c0001t0001g0062 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1242+55T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 10/13 | chr5 | 74718418 | ||||||
chr5:74718717
|
T | C | 1 | a0003c0003t0002g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1243-80T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 10/13 | chr5 | 74718717 | ||||||
chr5:74719187
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A | G | 1 | a0002c0002t0001g0327 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1417+216A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719187 | ||||||
chr5:74719200
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T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(42): Show | 53 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1417+229T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719200 | ||||||
chr5:74719341
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C | T | 1 | a0001c0001t0001g0041 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1417+370C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719341 | ||||||
chr5:74719409
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A | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(42): Show | 53 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1417+438A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719409 | ||||||
chr5:74719525
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A | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(152): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1417+554A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719525 | ||||||
chr5:74719622
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C | T | 1 | a0001c0001t0001g0027 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1417+651C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719622 | ||||||
chr5:74719709
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C | T | 1 | a0001c0001t0001g0077 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1418-719C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719709 | ||||||
chr5:74719815
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A | G | 10 | a0001c0001t0001g0039a0001c0001t0001g0227a0001c0001t0001g0245others(7): Show | 11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1418-613A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719815 | ||||||
chr5:74719876
|
G | A | 1 | a0001c0001t0001g0020 | 2 | NA18944.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1418-552G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719876 | ||||||
chr5:74719897
|
C | T | 1 | a0001c0001t0001g0027 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1418-531C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719897 | ||||||
chr5:74719940
|
C | CA | 50 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(47): Show | 59 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1418-473dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 74719940 | |||||
chr5:74719940
|
CA | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(7): Show | 13 | HG01943.hp2 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1418-473delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 74719940 | |||||
chr5:74719954
|
A | AAAAC | 52 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0022others(49): Show | 55 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1418-473_1418-472i others(6): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 74719954 | |||||
chr5:74719954
|
A | AAAC | 20 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0041others(17): Show | 22 | HG00642.hp1 HG00733.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1418-473_1418-472i others(5): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 74719954 | |||||
chr5:74719954
|
A | AC | 4 | a0001c0001t0001g0079a0002c0002t0001g0293a0002c0002t0001g0297others(1): Show | 4 | HG02602.hp1 HG02602.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1418-474_1418-473i others(3): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719954 | ||||||
chr5:74720032
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1418-396C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74720032 | ||||||
chr5:74720157
|
C | T | 1 | a0010c0008t0001g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1418-271C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74720157 | ||||||
chr5:74720165
|
C | T | 1 | a0002c0002t0001g0038 | 2 | NA18988.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1418-263C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74720165 | ||||||
chr5:74720231
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1418-197A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74720231 | ||||||
chr5:74720235
|
T | A | 3 | a0006c0007t0001g0055a0006c0007t0001g0057a0006c0007t0001g0178 | 3 | HG00642.hp1 HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1418-193T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74720235 | ||||||
chr5:74720619
|
G | A | 4 | a0002c0002t0002g0028a0002c0002t0002g0306a0002c0002t0002g0307others(1): Show | 5 | HG03704.hp2 NA18962.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1509-24G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 12/13 | chr5 | 74720619 | ||||||
chr5:74721041
|
AATATCAA others(21): Show |
A | 10 | a0001c0001t0001g0039a0001c0001t0001g0227a0001c0001t0001g0245others(7): Show | 11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1614-63_1614-36del others(28): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr5 | 74721041 | |||||
chr5:74721052
|
A | C | 1 | a0001c0001t0001g0246 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1614-66A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 13/13 | chr5 | 74721052 | ||||||
chr5:74721074
|
C | T | 1 | a0002c0002t0001g0279 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1614-44C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 13/13 | chr5 | 74721074 |