geneid | 9177 |
---|---|
ensemblid | ENSG00000149305.8 |
hgncid | 5298 |
symbol | HTR3B |
name | 5-hydroxytryptamine receptor 3B |
refseq_nuc | NM_006028.5 |
refseq_prot | NP_006019.1 |
ensembl_nuc | ENST00000260191.8 |
ensembl_prot | ENSP00000260191.2 |
mane_status | MANE Select |
chr | chr11 |
start | 113904796 |
end | 113949079 |
strand | + |
ver | v1.2 |
region | chr11:113904796-113949079 |
region5000 | chr11:113899796-113954079 |
regionname0 | HTR3B_chr11_113904796_113949079 |
regionname5000 | HTR3B_chr11_113899796_113954079 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 441 | 265 | 46 | 35 | 146 | 8 | 29 | 108 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002 | 0/1 | 441 | 135 | 29 | 36 | 49 | 3 | 17 | 43 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0003 | 0/0 | 441 | 10 | 6 | 3 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0004 | 0/0 | 441 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0005 | 0/0 | 441 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0006 | 0/0 | 441 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0007 | 0/0 | 441 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0008 | 0/0 | 441 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1326 | 205 | 39 | 30 | 102 | 8 | 25 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
c0002 | 0/1 | 1326 | 135 | 29 | 36 | 49 | 3 | 17 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
c0003 | 0/0 | 1326 | 53 | 2 | 5 | 44 | 0 | 2 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
c0004 | 0/0 | 1326 | 6 | 6 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
c0005 | 0/0 | 1326 | 5 | 5 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
c0006 | 0/0 | 1326 | 4 | 0 | 3 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
c0007 | 0/0 | 1326 | 4 | 4 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
c0008 | 0/0 | 1326 | 2 | 0 | 0 | 0 | 0 | 2 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
c0009 | 0/0 | 1326 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
c0010 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
c0011 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
c0012 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3070 | 62 | 8 | 11 | 34 | 0 | 9 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0002 | 0/0 | 3082 | 60 | 4 | 14 | 30 | 3 | 9 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0003 | 0/0 | 3083 | 49 | 1 | 5 | 43 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0004 | 0/0 | 3085 | 27 | 4 | 2 | 15 | 1 | 5 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0005 | 0/0 | 3075 | 27 | 2 | 3 | 17 | 0 | 5 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0006 | 0/0 | 3070 | 25 | 0 | 11 | 11 | 0 | 3 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0007 | 0/0 | 3081 | 22 | 9 | 4 | 9 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0008 | 0/1 | 3083 | 12 | 0 | 7 | 0 | 1 | 3 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0009 | 0/0 | 3086 | 11 | 0 | 1 | 8 | 0 | 2 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0010 | 0/0 | 3086 | 9 | 1 | 1 | 2 | 3 | 2 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0011 | 0/0 | 3078 | 8 | 8 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0012 | 0/0 | 3083 | 7 | 7 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0013 | 0/0 | 3079 | 6 | 0 | 0 | 6 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0014 | 0/0 | 3082 | 5 | 3 | 2 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0015 | 0/0 | 3070 | 5 | 0 | 0 | 5 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0016 | 0/0 | 3085 | 5 | 0 | 0 | 5 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0017 | 0/0 | 3086 | 4 | 3 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0018 | 0/0 | 3079 | 4 | 1 | 1 | 1 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0019 | 0/0 | 3080 | 4 | 4 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0020 | 0/0 | 3086 | 3 | 3 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0021 | 0/0 | 3083 | 3 | 3 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0022 | 0/0 | 3083 | 3 | 3 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0023 | 0/0 | 3085 | 3 | 0 | 3 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0024 | 0/0 | 3071 | 3 | 0 | 0 | 1 | 0 | 2 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0025 | 0/0 | 3085 | 3 | 3 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0026 | 0/0 | 3082 | 2 | 2 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0027 | 0/0 | 3082 | 2 | 0 | 1 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0028 | 0/0 | 3082 | 2 | 2 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0029 | 0/0 | 3079 | 2 | 0 | 0 | 0 | 2 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0030 | 0/0 | 3082 | 2 | 2 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0031 | 0/0 | 3076 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0032 | 0/0 | 3070 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0033 | 0/0 | 3070 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0034 | 0/0 | 3070 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0035 | 0/0 | 3094 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0036 | 0/0 | 3086 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0037 | 0/0 | 3085 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0038 | 0/0 | 3086 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0039 | 0/0 | 3086 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0040 | 0/0 | 3087 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0041 | 0/0 | 3082 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0042 | 0/0 | 3082 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0043 | 0/0 | 3082 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0044 | 0/0 | 3083 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0045 | 0/0 | 3084 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0046 | 0/0 | 3084 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0047 | 0/0 | 3083 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0048 | 0/0 | 3251 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0049 | 0/0 | 3083 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0050 | 0/0 | 3081 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0051 | 0/0 | 3082 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0052 | 1/0 | 3081 | 1 | 0 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0053 | 0/0 | 3445 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0054 | 0/0 | 3077 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0055 | 0/0 | 3079 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0056 | 0/0 | 3079 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0057 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0058 | 0/0 | 3070 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0059 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0060 | 0/0 | 3082 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0061 | 0/0 | 3089 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0062 | 0/0 | 3081 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0063 | 0/0 | 3144 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0064 | 0/0 | 3079 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0065 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0066 | 0/0 | 3074 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
t0067 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 4 | 0 | 0 | 0 | 3 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0002 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0006 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0361 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1326 | 205 | 39 | 30 | 102 | 8 | 25 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0003 | 0/0 | 1326 | 53 | 2 | 5 | 44 | 0 | 2 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0005 | 0/0 | 1326 | 5 | 5 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0008 | 0/0 | 1326 | 2 | 0 | 0 | 0 | 0 | 2 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002 | 0/1 | 1326 | 135 | 29 | 36 | 49 | 3 | 17 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0003c0004 | 0/0 | 1326 | 6 | 6 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0003c0006 | 0/0 | 1326 | 4 | 0 | 3 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0004c0007 | 0/0 | 1326 | 4 | 4 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0005c0009 | 0/0 | 1326 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0006c0012 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0007c0011 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0008c0010 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 4407 | 57 | 4 | 13 | 29 | 3 | 8 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0004 | 0/0 | 4410 | 27 | 4 | 2 | 15 | 1 | 5 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0005 | 0/0 | 4400 | 27 | 2 | 3 | 17 | 0 | 5 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0006 | 0/0 | 4395 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0007 | 0/0 | 4406 | 22 | 9 | 4 | 9 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0009 | 0/0 | 4411 | 11 | 0 | 1 | 8 | 0 | 2 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0010 | 0/0 | 4411 | 8 | 1 | 1 | 2 | 3 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0011 | 0/0 | 4403 | 8 | 8 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0013 | 0/0 | 4404 | 6 | 0 | 0 | 6 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0016 | 0/0 | 4410 | 5 | 0 | 0 | 5 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0017 | 0/0 | 4411 | 3 | 2 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0018 | 0/0 | 4404 | 4 | 1 | 1 | 1 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0026 | 0/0 | 4407 | 2 | 2 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0027 | 0/0 | 4407 | 2 | 0 | 1 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0031 | 0/0 | 4401 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0035 | 0/0 | 4419 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0036 | 0/0 | 4411 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0037 | 0/0 | 4410 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0038 | 0/0 | 4411 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0039 | 0/0 | 4411 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0040 | 0/0 | 4412 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0041 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0042 | 0/0 | 4407 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0043 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0050 | 0/0 | 4406 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0051 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0052 | 1/0 | 4406 | 1 | 0 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0053 | 0/0 | 4770 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0054 | 0/0 | 4402 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0057 | 0/0 | 4403 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0060 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0062 | 0/0 | 4406 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0064 | 0/0 | 4404 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0066 | 0/0 | 4399 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0001t0067 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0003t0003 | 0/0 | 4408 | 49 | 1 | 5 | 43 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0003t0021 | 0/0 | 4408 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0003t0047 | 0/0 | 4408 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0003t0048 | 0/0 | 4576 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0003t0049 | 0/0 | 4408 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0005t0021 | 0/0 | 4408 | 2 | 2 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0005t0022 | 0/0 | 4408 | 3 | 3 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0008t0002 | 0/0 | 4407 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0001c0008t0010 | 0/0 | 4411 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0001 | 0/0 | 4395 | 61 | 8 | 11 | 33 | 0 | 9 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0002 | 0/0 | 4407 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0006 | 0/0 | 4395 | 24 | 0 | 11 | 10 | 0 | 3 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0008 | 0/1 | 4408 | 12 | 0 | 7 | 0 | 1 | 3 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0012 | 0/0 | 4408 | 7 | 7 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0014 | 0/0 | 4407 | 5 | 3 | 2 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0015 | 0/0 | 4395 | 5 | 0 | 0 | 5 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0020 | 0/0 | 4411 | 3 | 3 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0024 | 0/0 | 4396 | 3 | 0 | 0 | 1 | 0 | 2 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0028 | 0/0 | 4407 | 2 | 2 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0029 | 0/0 | 4404 | 2 | 0 | 0 | 0 | 2 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0032 | 0/0 | 4395 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0033 | 0/0 | 4395 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0034 | 0/0 | 4395 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0044 | 0/0 | 4408 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0045 | 0/0 | 4409 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0055 | 0/0 | 4404 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0056 | 0/0 | 4404 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0058 | 0/0 | 4395 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0059 | 0/0 | 4382 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0002c0002t0063 | 0/0 | 4469 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0003c0004t0025 | 0/0 | 4410 | 3 | 3 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0003c0004t0030 | 0/0 | 4407 | 2 | 2 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0003c0004t0061 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0003c0006t0023 | 0/0 | 4410 | 3 | 0 | 3 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0003c0006t0046 | 0/0 | 4409 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0004c0007t0019 | 0/0 | 4405 | 4 | 4 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0005c0009t0017 | 0/0 | 4411 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0006c0012t0065 | 0/0 | 4401 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0007c0011t0001 | 0/0 | 4395 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
a0008c0010t0002 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | copy fasta | chr11 | 113899796 | 113954079 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0004g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0007g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0009g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0009g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0009g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0009g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0009g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0009g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0009g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0009g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0009g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0009g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0009g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0010g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0010g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0010g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0010g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0010g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0010g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0010g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0011g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0011g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0011g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0011g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0011g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0011g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0013g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0013g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0013g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0013g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0013g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0013g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0016g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0016g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0016g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0016g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0016g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0017g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0017g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0017g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0018g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0018g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0018g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0018g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0026g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0026g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0027g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0027g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0031g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0031g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0035g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0036g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0037g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0038g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0039g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0040g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0041g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0042g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0043g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0050g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0051g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0052g0361 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0053g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0054g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0057g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0060g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0062g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0064g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0066g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0001t0067g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0021g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0047g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0048g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0003t0049g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0005t0021g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0005t0021g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0005t0022g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0005t0022g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0005t0022g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0008t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0001c0008t0010g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0002g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0002 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0006g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0008g0001 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0008g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0008g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0008g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0008g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0008g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0008g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0008g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0008g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0008g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0012g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0012g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0012g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0012g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0014g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0014g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0014g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0014g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0014g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0015g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0015g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0015g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0015g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0015g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0020g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0020g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0020g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0024g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0024g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0024g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0028g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0029g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0032g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0033g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0034g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0044g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0045g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0055g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0056g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0058g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0059g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0002c0002t0063g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0003c0004t0025g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0003c0004t0025g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0003c0004t0025g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0003c0004t0030g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0003c0004t0030g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0003c0004t0061g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0003c0006t0023g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0003c0006t0023g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0003c0006t0023g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0003c0006t0046g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0004c0007t0019g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0004c0007t0019g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0004c0007t0019g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0004c0007t0019g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0005c0009t0017g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0006c0012t0065g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0007c0011t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
a0008c0010t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0341 | EUR | GBR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00140 | hp2 | a0001 | c0001 | t0010 | g0019 | EUR | GBR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00323 | hp1 | a0001 | c0001 | t0010 | g0339 | EUR | FIN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00323 | hp2 | a0003 | c0006 | t0046 | g0139 | EUR | FIN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00408 | hp1 | a0001 | c0001 | t0009 | g0356 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00408 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00423 | hp1 | a0002 | c0002 | t0006 | g0176 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00423 | hp2 | a0001 | c0003 | t0003 | g0075 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00438 | hp1 | a0001 | c0003 | t0003 | g0008 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00544 | hp1 | a0001 | c0003 | t0003 | g0105 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00544 | hp2 | a0001 | c0001 | t0009 | g0022 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00558 | hp2 | a0001 | c0001 | t0013 | g0334 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0378 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00621 | hp1 | a0001 | c0003 | t0003 | g0099 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00621 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0366 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0304 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00642 | hp1 | a0002 | c0002 | t0006 | g0170 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00642 | hp2 | a0001 | c0001 | t0053 | g0069 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00673 | hp2 | a0001 | c0003 | t0003 | g0007 | EAS | CHS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00735 | hp2 | a0001 | c0001 | t0009 | g0199 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00738 | hp1 | a0002 | c0002 | t0014 | g0225 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0265 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0063 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG00741 | hp2 | a0001 | c0001 | t0010 | g0194 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01069 | hp1 | a0002 | c0002 | t0008 | g0214 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01069 | hp2 | a0002 | c0002 | t0006 | g0002 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01070 | hp1 | a0001 | c0001 | t0027 | g0312 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01070 | hp2 | a0002 | c0002 | t0006 | g0002 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01071 | hp1 | a0002 | c0002 | t0006 | g0002 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01071 | hp2 | a0002 | c0002 | t0008 | g0013 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01074 | hp1 | a0002 | c0002 | t0008 | g0215 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0365 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01081 | hp1 | a0001 | c0001 | t0018 | g0048 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0323 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01099 | hp1 | a0002 | c0002 | t0014 | g0224 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01109 | hp1 | a0002 | c0002 | t0008 | g0013 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01109 | hp2 | a0002 | c0002 | t0056 | g0220 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01167 | hp1 | a0001 | c0001 | t0007 | g0303 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0237 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01169 | hp1 | a0001 | c0001 | t0007 | g0306 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0165 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01175 | hp2 | a0002 | c0002 | t0044 | g0149 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01192 | hp1 | a0002 | c0002 | t0008 | g0212 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01192 | hp2 | a0001 | c0003 | t0003 | g0079 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01243 | hp1 | a0001 | c0001 | t0007 | g0121 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01243 | hp2 | a0001 | c0001 | t0017 | g0119 | AMR | PUR | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01255 | hp1 | a0002 | c0002 | t0008 | g0140 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0355 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01256 | hp1 | a0003 | c0006 | t0023 | g0207 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0064 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01261 | hp2 | a0001 | c0001 | t0062 | g0027 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0354 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01346 | hp2 | a0001 | c0003 | t0003 | g0098 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01361 | hp2 | a0001 | c0001 | t0036 | g0184 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0362 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01433 | hp2 | a0002 | c0002 | t0008 | g0213 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01496 | hp2 | a0002 | c0002 | t0006 | g0175 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0006 | EUR | IBS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01515 | hp2 | a0002 | c0002 | t0029 | g0001 | EUR | IBS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01516 | hp1 | a0002 | c0002 | t0008 | g0001 | EUR | IBS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0311 | EUR | IBS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01517 | hp1 | a0002 | c0002 | t0029 | g0001 | EUR | IBS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0367 | EUR | IBS | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01884 | hp1 | a0001 | c0001 | t0067 | g0054 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01884 | hp2 | a0003 | c0004 | t0030 | g0222 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01891 | hp1 | a0004 | c0007 | t0019 | g0315 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01891 | hp2 | a0001 | c0005 | t0022 | g0384 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0034 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0234 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01952 | hp1 | a0001 | c0003 | t0003 | g0100 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01952 | hp2 | a0003 | c0006 | t0023 | g0206 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0359 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0231 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01978 | hp1 | a0001 | c0003 | t0003 | g0078 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01978 | hp2 | a0002 | c0002 | t0006 | g0273 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01981 | hp1 | a0002 | c0002 | t0006 | g0173 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0247 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01993 | hp1 | a0002 | c0002 | t0006 | g0276 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0342 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02004 | hp1 | a0001 | c0003 | t0003 | g0101 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0292 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0379 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02015 | hp2 | a0001 | c0003 | t0003 | g0086 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02027 | hp1 | a0001 | c0001 | t0009 | g0197 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02027 | hp2 | a0001 | c0003 | t0003 | g0082 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02040 | hp1 | a0001 | c0003 | t0003 | g0074 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02055 | hp1 | a0001 | c0001 | t0026 | g0115 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0124 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0373 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02074 | hp2 | a0001 | c0001 | t0051 | g0332 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02080 | hp2 | a0001 | c0003 | t0003 | g0102 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02083 | hp1 | a0001 | c0003 | t0003 | g0096 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0041 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02129 | hp2 | a0001 | c0001 | t0007 | g0179 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02132 | hp2 | a0001 | c0003 | t0003 | g0094 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02135 | hp1 | a0001 | c0001 | t0013 | g0060 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02135 | hp2 | a0001 | c0003 | t0003 | g0085 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02145 | hp1 | a0001 | c0001 | t0057 | g0167 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02145 | hp2 | a0002 | c0002 | t0045 | g0147 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02148 | hp1 | a0002 | c0002 | t0033 | g0163 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02148 | hp2 | a0002 | c0002 | t0006 | g0172 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02155 | hp1 | a0001 | c0003 | t0003 | g0095 | EAS | CDX | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | CDX | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0135 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02257 | hp2 | a0001 | c0003 | t0021 | g0073 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02258 | hp1 | a0004 | c0007 | t0019 | g0316 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02273 | hp2 | a0002 | c0002 | t0032 | g0275 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02280 | hp1 | a0002 | c0002 | t0028 | g0012 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02280 | hp2 | a0001 | c0001 | t0011 | g0282 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02293 | hp2 | a0002 | c0002 | t0006 | g0272 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02300 | hp1 | a0003 | c0006 | t0023 | g0205 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02300 | hp2 | a0002 | c0002 | t0006 | g0174 | AMR | PEL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0126 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0049 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | KHV | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0168 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02602 | hp1 | a0001 | c0003 | t0048 | g0087 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0047 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0266 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02622 | hp2 | a0001 | c0005 | t0021 | g0383 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02647 | hp1 | a0001 | c0003 | t0003 | g0077 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02647 | hp2 | a0001 | c0001 | t0017 | g0116 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02683 | hp1 | a0002 | c0002 | t0008 | g0209 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02683 | hp2 | a0001 | c0008 | t0002 | g0326 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0309 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0344 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02717 | hp1 | a0002 | c0002 | t0012 | g0148 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02717 | hp2 | a0002 | c0002 | t0055 | g0277 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02723 | hp1 | a0001 | c0001 | t0017 | g0117 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02723 | hp2 | a0003 | c0004 | t0061 | g0141 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02735 | hp1 | a0002 | c0002 | t0024 | g0269 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0261 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02738 | hp1 | a0001 | c0001 | t0009 | g0363 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0035 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02809 | hp1 | a0004 | c0007 | t0019 | g0314 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0131 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02818 | hp1 | a0004 | c0007 | t0019 | g0313 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02818 | hp2 | a0002 | c0002 | t0034 | g0271 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0369 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02886 | hp2 | a0002 | c0002 | t0014 | g0221 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0143 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0208 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0264 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02897 | hp2 | a0001 | c0001 | t0011 | g0281 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0371 | AFR | ESN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02922 | hp2 | a0002 | c0002 | t0014 | g0226 | AFR | ESN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02970 | hp1 | a0001 | c0001 | t0040 | g0120 | AFR | ESN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02970 | hp2 | a0001 | c0005 | t0022 | g0386 | AFR | ESN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0129 | AFR | ESN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02976 | hp2 | a0001 | c0001 | t0011 | g0113 | AFR | ESN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03017 | hp1 | a0001 | c0008 | t0010 | g0358 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03017 | hp2 | a0002 | c0002 | t0024 | g0268 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03041 | hp1 | a0003 | c0004 | t0025 | g0151 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03041 | hp2 | a0002 | c0002 | t0012 | g0218 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03098 | hp1 | a0003 | c0004 | t0030 | g0223 | AFR | MSL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0169 | AFR | MSL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03130 | hp1 | a0002 | c0002 | t0059 | g0262 | AFR | ESN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03130 | hp2 | a0002 | c0002 | t0020 | g0203 | AFR | ESN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03195 | hp1 | a0002 | c0002 | t0012 | g0211 | AFR | ESN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03195 | hp2 | a0002 | c0002 | t0012 | g0133 | AFR | ESN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | MSL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03209 | hp2 | a0002 | c0002 | t0063 | g0024 | AFR | MSL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03239 | hp1 | a0002 | c0002 | t0006 | g0260 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0242 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03453 | hp1 | a0002 | c0002 | t0012 | g0217 | AFR | MSL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | MSL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03486 | hp1 | a0001 | c0001 | t0011 | g0178 | AFR | MSL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0122 | AFR | MSL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03492 | hp2 | a0002 | c0002 | t0006 | g0002 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03516 | hp1 | a0001 | c0005 | t0022 | g0385 | AFR | ESN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03516 | hp2 | a0001 | c0001 | t0041 | g0134 | AFR | ESN | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03540 | hp1 | a0002 | c0002 | t0012 | g0219 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | GWD | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03579 | hp1 | a0002 | c0002 | t0012 | g0216 | AFR | MSL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03579 | hp2 | a0001 | c0001 | t0064 | g0025 | AFR | MSL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0302 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03654 | hp2 | a0001 | c0003 | t0049 | g0088 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03669 | hp1 | a0001 | c0001 | t0010 | g0340 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0055 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0360 | SAS | STU | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03688 | hp2 | a0002 | c0002 | t0006 | g0137 | SAS | STU | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0305 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03704 | hp2 | a0001 | c0001 | t0035 | g0351 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0040 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0238 | SAS | PJL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03831 | hp1 | a0002 | c0002 | t0008 | g0146 | SAS | BEB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03831 | hp2 | a0001 | c0001 | t0018 | g0061 | SAS | BEB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | BEB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03834 | hp2 | a0002 | c0002 | t0008 | g0210 | SAS | BEB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0350 | SAS | BEB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03927 | hp2 | a0001 | c0001 | t0009 | g0345 | SAS | BEB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03942 | hp1 | a0001 | c0001 | t0050 | g0177 | SAS | BEB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0232 | SAS | BEB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0308 | SAS | STU | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG04115 | hp2 | a0001 | c0001 | t0039 | g0357 | SAS | STU | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0280 | SAS | STU | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0180 | SAS | STU | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | STU | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0196 | SAS | STU | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0164 | SAS | STU | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0291 | SAS | STU | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18522 | hp1 | a0001 | c0001 | t0011 | g0283 | AFR | YRI | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18522 | hp2 | a0002 | c0002 | t0020 | g0144 | AFR | YRI | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | CHB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18612 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | CHB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18747 | hp1 | a0001 | c0003 | t0003 | g0108 | EAS | CHB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18747 | hp2 | a0002 | c0002 | t0006 | g0270 | EAS | CHB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18939 | hp1 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18941 | hp1 | a0001 | c0003 | t0047 | g0106 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0374 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18942 | hp2 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18943 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18944 | hp1 | a0001 | c0001 | t0013 | g0059 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18944 | hp2 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18946 | hp1 | a0001 | c0001 | t0016 | g0298 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18946 | hp2 | a0001 | c0003 | t0003 | g0093 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18947 | hp1 | a0001 | c0001 | t0009 | g0364 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18948 | hp1 | a0001 | c0003 | t0003 | g0092 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18949 | hp1 | a0001 | c0003 | t0003 | g0080 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18951 | hp1 | a0001 | c0001 | t0066 | g0031 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18951 | hp2 | a0001 | c0001 | t0016 | g0295 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0377 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18953 | hp1 | a0001 | c0001 | t0016 | g0285 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18954 | hp1 | a0001 | c0003 | t0003 | g0072 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18959 | hp1 | a0001 | c0001 | t0016 | g0278 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18960 | hp1 | a0001 | c0001 | t0007 | g0286 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18960 | hp2 | a0001 | c0003 | t0003 | g0103 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18962 | hp1 | a0001 | c0001 | t0010 | g0343 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18962 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18963 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18965 | hp1 | a0001 | c0003 | t0003 | g0111 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18966 | hp1 | a0001 | c0001 | t0009 | g0198 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18966 | hp2 | a0001 | c0001 | t0010 | g0382 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18967 | hp1 | a0006 | c0012 | t0065 | g0030 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18968 | hp2 | a0008 | c0010 | t0002 | g0296 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18969 | hp1 | a0001 | c0001 | t0037 | g0161 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18969 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18973 | hp1 | a0002 | c0002 | t0006 | g0274 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18974 | hp1 | a0002 | c0002 | t0006 | g0204 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18979 | hp2 | a0001 | c0001 | t0007 | g0294 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18980 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18980 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18981 | hp1 | a0001 | c0003 | t0003 | g0083 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18983 | hp1 | a0001 | c0001 | t0031 | g0045 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18985 | hp2 | a0001 | c0001 | t0007 | g0183 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18986 | hp1 | a0002 | c0002 | t0006 | g0112 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18986 | hp2 | a0002 | c0002 | t0015 | g0289 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18989 | hp1 | a0001 | c0003 | t0003 | g0114 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18989 | hp2 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18990 | hp1 | a0002 | c0002 | t0006 | g0011 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18990 | hp2 | a0001 | c0001 | t0043 | g0192 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18991 | hp1 | a0002 | c0002 | t0024 | g0259 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18991 | hp2 | a0001 | c0003 | t0003 | g0109 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18992 | hp2 | a0001 | c0001 | t0007 | g0287 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0381 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18993 | hp2 | a0001 | c0003 | t0003 | g0084 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18995 | hp1 | a0001 | c0003 | t0003 | g0097 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18998 | hp1 | a0001 | c0001 | t0013 | g0058 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18998 | hp2 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19000 | hp1 | a0001 | c0003 | t0003 | g0081 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19001 | hp1 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19001 | hp2 | a0001 | c0003 | t0003 | g0090 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19002 | hp1 | a0002 | c0002 | t0006 | g0166 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19002 | hp2 | a0002 | c0002 | t0006 | g0011 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19003 | hp1 | a0001 | c0003 | t0003 | g0091 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19004 | hp1 | a0001 | c0003 | t0003 | g0007 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19005 | hp1 | a0001 | c0001 | t0031 | g0033 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19007 | hp1 | a0001 | c0001 | t0013 | g0038 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19007 | hp2 | a0001 | c0003 | t0003 | g0104 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19009 | hp1 | a0007 | c0011 | t0001 | g0235 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19010 | hp1 | a0001 | c0003 | t0003 | g0071 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19012 | hp1 | a0001 | c0001 | t0038 | g0375 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19030 | hp1 | a0002 | c0002 | t0020 | g0145 | AFR | LWK | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19030 | hp2 | a0003 | c0004 | t0025 | g0070 | AFR | LWK | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0130 | AFR | LWK | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19043 | hp2 | a0002 | c0002 | t0058 | g0370 | AFR | LWK | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19054 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19055 | hp1 | a0001 | c0001 | t0006 | g0193 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19056 | hp1 | a0001 | c0001 | t0009 | g0348 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19058 | hp2 | a0002 | c0002 | t0015 | g0252 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19060 | hp1 | a0002 | c0002 | t0015 | g0160 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19060 | hp2 | a0001 | c0001 | t0027 | g0022 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19062 | hp2 | a0001 | c0001 | t0018 | g0036 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19063 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19064 | hp1 | a0001 | c0001 | t0007 | g0288 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19064 | hp2 | a0001 | c0001 | t0013 | g0052 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19065 | hp1 | a0001 | c0001 | t0054 | g0380 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19068 | hp2 | a0001 | c0001 | t0016 | g0181 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19070 | hp2 | a0001 | c0001 | t0007 | g0301 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19074 | hp1 | a0001 | c0001 | t0009 | g0347 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19077 | hp1 | a0001 | c0003 | t0003 | g0089 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19077 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19079 | hp1 | a0001 | c0003 | t0003 | g0076 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19079 | hp2 | a0002 | c0002 | t0015 | g0159 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19080 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19082 | hp1 | a0001 | c0003 | t0003 | g0107 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19084 | hp2 | a0001 | c0003 | t0003 | g0110 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19085 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0372 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19089 | hp1 | a0001 | c0001 | t0007 | g0376 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19089 | hp2 | a0002 | c0002 | t0006 | g0267 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19090 | hp1 | a0001 | c0001 | t0009 | g0346 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19090 | hp2 | a0002 | c0002 | t0006 | g0171 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19091 | hp1 | a0002 | c0002 | t0015 | g0249 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19091 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19240 | hp1 | a0003 | c0004 | t0025 | g0152 | AFR | YRI | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA19240 | hp2 | a0002 | c0002 | t0014 | g0150 | AFR | YRI | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA20129 | hp1 | a0001 | c0001 | t0018 | g0051 | AFR | ASW | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | ASW | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA20805 | hp1 | a0001 | c0001 | t0042 | g0307 | EUR | TSI | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA20805 | hp2 | a0001 | c0001 | t0010 | g0019 | EUR | TSI | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA20905 | hp1 | a0001 | c0001 | t0005 | g0053 | SAS | GIH | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | GIH | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01123 | hp1 | a0001 | c0001 | t0007 | g0125 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | CLM | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02109 | hp1 | a0001 | c0001 | t0010 | g0324 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02109 | hp2 | a0002 | c0002 | t0028 | g0012 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02486 | hp1 | a0005 | c0009 | t0017 | g0318 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02486 | hp2 | a0001 | c0001 | t0026 | g0118 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0284 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0187 | AFR | ACB | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0263 | AFR | MSL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | MSL | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0368 | AFR | USA | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA20300 | hp2 | a0001 | c0001 | t0060 | g0195 | AFR | USA | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA21309 | hp1 | a0001 | c0005 | t0021 | g0068 | AFR | LWK | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0026 | AFR | LWK | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0008 | g0001 | REF | REF | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0052 | g0361 | REF | REF | HTR3B_chr11_113899796_113954079 | HTR3B | chr11 | 113899796 | 113954079 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:113904944
|
G | A | 1 | a0005 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.11G>A | p.Ser4Asn | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/9 | 149/4406 | 11/1326 | 4/441 | chr11 | 113904944 | ||
chr11:113932306
|
A | C | 4 | a0002a0003a0004others(1): Show | 150 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(147): Show |
missense_variant | MODERATE | c.386A>C | p.Tyr129Ser | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 5/9 | 524/4406 | 386/1326 | 129/441 | chr11 | 113932306 | ||
chr11:113932306
|
A | G | 1 | a0006 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.386A>G | p.Tyr129Cys | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 5/9 | 524/4406 | 386/1326 | 129/441 | chr11 | 113932306 | ||
chr11:113932348
|
T | C | 1 | a0008 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.428T>C | p.Ile143Thr | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 5/9 | 566/4406 | 428/1326 | 143/441 | chr11 | 113932348 | ||
chr11:113932944
|
G | A | 1 | a0003 | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
missense_variant | MODERATE | c.547G>A | p.Val183Ile | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/9 | 685/4406 | 547/1326 | 183/441 | chr11 | 113932944 | ||
chr11:113943144
|
A | T | 1 | a0007 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.859A>T | p.Asn287Tyr | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/9 | 997/4406 | 859/1326 | 287/441 | chr11 | 113943144 | ||
chr11:113943170
|
T | A | 1 | a0007 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.885T>A | p.Ser295Arg | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/9 | 1023/4406 | 885/1326 | 295/441 | chr11 | 113943170 | ||
chr11:113944725
|
G | A | 1 | a0004 | 4 | HG01891.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
missense_variant | MODERATE | c.1060G>A | p.Glu354Lys | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/9 | 1198/4406 | 1060/1326 | 354/441 | chr11 | 113944725 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:113932382
|
G | A | 2 | a0001c0003a0003c0004 | 59 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
synonymous_variant | LOW | c.462G>A | p.Ala154Ala | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 5/9 | 600/4406 | 462/1326 | 154/441 | chr11 | 113932382 | ||
chr11:113932382
|
G | C | 1 | a0001c0005 | 5 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(2): Show |
synonymous_variant | LOW | c.462G>C | p.Ala154Ala | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 5/9 | 600/4406 | 462/1326 | 154/441 | chr11 | 113932382 | ||
chr11:113943176
|
G | T | 1 | a0007c0011 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.891G>T | p.Gly297Gly | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/9 | 1029/4406 | 891/1326 | 297/441 | chr11 | 113943176 | ||
chr11:113946128
|
C | T | 1 | a0001c0008 | 2 | HG02683.hp2 HG03017.hp1 |
synonymous_variant | LOW | c.1317C>T | p.Gly439Gly | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 1455/4406 | 1317/1326 | 439/441 | chr11 | 113946128 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:113904827
|
C | CGGAGAAG others(54): Show |
1 | a0002c0002t0063 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-106_-46dupGGAGAAG others(54): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/9 | 45 | INFO_REALIGN_3_PRIME | chr11 | 113904827 | ||||
chr11:113904829
|
GAGA | G | 9 | a0001c0001t0005a0001c0001t0013a0001c0001t0018others(6): Show | 47 | HG00558.hp2 HG00741.hp1 HG01081.hp1 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-102_-100delAAG | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/9 | 100 | INFO_REALIGN_3_PRIME | chr11 | 113904829 | ||||
chr11:113904870
|
A | G | 1 | a0001c0001t0016 | 5 | NA18946.hp1 NA18951.hp2 NA18953.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-64A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/9 | 64 | chr11 | 113904870 | |||||
chr11:113904873
|
T | C | 1 | a0001c0001t0026 | 2 | HG02055.hp1 HG02486.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-61T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/9 | chr11 | 113904873 | ||||||
chr11:113904891
|
G | A | 1 | a0002c0002t0032 | 1 | HG02273.hp2 | 5_prime_UTR_variant | MODIFIER | c.-43G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/9 | 43 | chr11 | 113904891 | |||||
chr11:113904931
|
G | A | 1 | a0002c0002t0033 | 1 | HG02148.hp1 | 5_prime_UTR_variant | MODIFIER | c.-3G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/9 | 3 | chr11 | 113904931 | |||||
chr11:113946150
|
T | C | 1 | a0002c0002t0034 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 13 | chr11 | 113946150 | |||||
chr11:113946222
|
C | T | 4 | a0001c0001t0062a0003c0004t0025a0003c0004t0030others(1): Show | 7 | HG01261.hp2 HG01884.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*85C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 85 | chr11 | 113946222 | |||||
chr11:113946276
|
G | T | 1 | a0001c0001t0060 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*139G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 139 | chr11 | 113946276 | |||||
chr11:113946340
|
G | GTAAA | 14 | a0001c0001t0004a0001c0001t0009a0001c0001t0010others(11): Show | 65 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*242_*245dupAATA | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 246 | INFO_REALIGN_3_PRIME | chr11 | 113946340 | ||||
chr11:113946340
|
G | GTAAATAA others(5): Show |
1 | a0001c0001t0035 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*234_*245dupAATAAA others(6): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 246 | INFO_REALIGN_3_PRIME | chr11 | 113946340 | ||||
chr11:113946340
|
GTAAA | G | 10 | a0001c0001t0005a0001c0001t0011a0001c0001t0031others(7): Show | 45 | HG00741.hp1 HG01109.hp2 HG01261.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*242_*245delAATA | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 242 | INFO_REALIGN_3_PRIME | chr11 | 113946340 | ||||
chr11:113946340
|
GTAAATAA others(5): Show |
G | 12 | a0001c0001t0006a0001c0001t0067a0002c0002t0001others(9): Show | 101 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*234_*245delAATAAA others(6): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 234 | INFO_REALIGN_3_PRIME | chr11 | 113946340 | ||||
chr11:113946564
|
G | A | 13 | a0001c0001t0004a0001c0001t0007a0001c0001t0009others(10): Show | 75 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*427G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 427 | chr11 | 113946564 | |||||
chr11:113946746
|
C | T | 10 | a0001c0001t0004a0001c0001t0007a0001c0001t0016others(7): Show | 61 | HG00597.hp2 HG00639.hp2 HG01099.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*609C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 609 | chr11 | 113946746 | |||||
chr11:113946820
|
G | A | 1 | a0001c0001t0043 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*683G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 683 | chr11 | 113946820 | |||||
chr11:113946857
|
T | C | 12 | a0001c0001t0006a0001c0001t0039a0002c0002t0001others(9): Show | 101 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*720T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 720 | chr11 | 113946857 | |||||
chr11:113946934
|
T | A | 56 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(53): Show | 320 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*797T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 797 | chr11 | 113946934 | |||||
chr11:113946958
|
T | C | 13 | a0001c0001t0006a0001c0001t0036a0001c0001t0039others(10): Show | 102 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*821T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 821 | chr11 | 113946958 | |||||
chr11:113947047
|
C | T | 4 | a0001c0003t0003a0001c0003t0047a0001c0003t0048others(1): Show | 52 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*910C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 910 | chr11 | 113947047 | |||||
chr11:113947109
|
C | CT | 7 | a0001c0001t0031a0001c0001t0038a0003c0004t0025others(4): Show | 13 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*985dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 986 | INFO_REALIGN_3_PRIME | chr11 | 113947109 | ||||
chr11:113947229
|
G | A | 3 | a0002c0002t0008a0002c0002t0029a0002c0002t0044 | 15 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1092G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 1092 | chr11 | 113947229 | |||||
chr11:113947415
|
C | T | 1 | a0001c0001t0057 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1278C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 1278 | chr11 | 113947415 | |||||
chr11:113947503
|
A | G | 1 | a0001c0003t0049 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1366A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 1366 | chr11 | 113947503 | |||||
chr11:113947549
|
T | C | 13 | a0001c0001t0006a0001c0001t0036a0001c0001t0039others(10): Show | 102 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1412T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 1412 | chr11 | 113947549 | |||||
chr11:113947566
|
A | ACTTCTTG others(356): Show |
1 | a0001c0001t0053 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1446_*1447insTTTT others(359): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 1447 | INFO_REALIGN_3_PRIME | chr11 | 113947566 | ||||
chr11:113947607
|
C | T | 13 | a0001c0001t0006a0001c0001t0036a0001c0001t0039others(10): Show | 102 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1470C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 1470 | chr11 | 113947607 | |||||
chr11:113947741
|
T | C | 6 | a0001c0003t0003a0001c0003t0021a0001c0003t0047others(3): Show | 55 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1604T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 1604 | chr11 | 113947741 | |||||
chr11:113947785
|
A | T | 2 | a0003c0006t0023a0003c0006t0046 | 4 | HG00323.hp2 HG01256.hp1 HG01952.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1648A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 1648 | chr11 | 113947785 | |||||
chr11:113948030
|
C | A | 43 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(40): Show | 278 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*1893C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 1893 | chr11 | 113948030 | |||||
chr11:113948061
|
T | C | 3 | a0001c0001t0006a0002c0002t0006a0002c0002t0032 | 26 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1924T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 1924 | chr11 | 113948061 | |||||
chr11:113948069
|
G | A | 1 | a0001c0003t0047 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1932G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 1932 | chr11 | 113948069 | |||||
chr11:113948252
|
G | C | 3 | a0002c0002t0020a0002c0002t0028a0004c0007t0019 | 9 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2115G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2115 | chr11 | 113948252 | |||||
chr11:113948414
|
G | C | 1 | a0001c0001t0051 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2277G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2277 | chr11 | 113948414 | |||||
chr11:113948520
|
T | C | 1 | a0002c0002t0058 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2383T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2383 | chr11 | 113948520 | |||||
chr11:113948557
|
T | A | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2420T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2420 | chr11 | 113948557 | |||||
chr11:113948568
|
T | C | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2431T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2431 | chr11 | 113948568 | |||||
chr11:113948570
|
T | A | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2433T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2433 | chr11 | 113948570 | |||||
chr11:113948571
|
G | T | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2434G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2434 | chr11 | 113948571 | |||||
chr11:113948574
|
A | T | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2437A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2437 | chr11 | 113948574 | |||||
chr11:113948575
|
A | C | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2438A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2438 | chr11 | 113948575 | |||||
chr11:113948576
|
G | C | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2439G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2439 | chr11 | 113948576 | |||||
chr11:113948577
|
T | C | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2440T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2440 | chr11 | 113948577 | |||||
chr11:113948580
|
A | T | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2443A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2443 | chr11 | 113948580 | |||||
chr11:113948581
|
T | C | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2444T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2444 | chr11 | 113948581 | |||||
chr11:113948583
|
A | C | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2446A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2446 | chr11 | 113948583 | |||||
chr11:113948584
|
TGGGGCGT others(6): Show |
T | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2448_*2460delGGGG others(9): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2448 | chr11 | 113948584 | |||||
chr11:113948599
|
C | T | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2462C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2462 | chr11 | 113948599 | |||||
chr11:113948600
|
A | G | 1 | a0002c0002t0059 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2463A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2463 | chr11 | 113948600 | |||||
chr11:113948656
|
G | GAGTTTGA others(161): Show |
1 | a0001c0003t0048 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2520_*2687dupAGTT others(164): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2688 | INFO_REALIGN_3_PRIME | chr11 | 113948656 | ||||
chr11:113948661
|
T | C | 2 | a0001c0005t0022a0002c0002t0055 | 4 | HG01891.hp2 HG02717.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2524T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2524 | chr11 | 113948661 | |||||
chr11:113948680
|
A | G | 1 | a0004c0007t0019 | 4 | HG01891.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2543A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2543 | chr11 | 113948680 | |||||
chr11:113948723
|
C | T | 1 | a0002c0002t0044 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2586C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2586 | chr11 | 113948723 | |||||
chr11:113948730
|
G | A | 13 | a0001c0001t0006a0001c0001t0036a0001c0001t0039others(10): Show | 102 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*2593G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2593 | chr11 | 113948730 | |||||
chr11:113948756
|
G | C | 1 | a0001c0001t0037 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2619G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2619 | chr11 | 113948756 | |||||
chr11:113948767
|
G | A | 1 | a0002c0002t0015 | 5 | NA18986.hp2 NA19058.hp2 NA19060.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2630G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2630 | chr11 | 113948767 | |||||
chr11:113948863
|
C | CA | 41 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(38): Show | 254 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*2740dupA | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2741 | INFO_REALIGN_3_PRIME | chr11 | 113948863 | ||||
chr11:113948863
|
C | CAA | 19 | a0001c0001t0040a0001c0003t0003a0001c0003t0021others(16): Show | 93 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2739_*2740dupAA | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2741 | INFO_REALIGN_3_PRIME | chr11 | 113948863 | ||||
chr11:113948863
|
C | CAAA | 4 | a0002c0002t0045a0003c0004t0025a0003c0004t0061others(1): Show | 8 | HG01256.hp1 HG01952.hp2 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2738_*2740dupAAA | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2741 | INFO_REALIGN_3_PRIME | chr11 | 113948863 | ||||
chr11:113948952
|
C | T | 5 | a0001c0001t0005a0001c0001t0018a0001c0001t0031others(2): Show | 35 | HG00741.hp1 HG01081.hp1 HG01261.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2815C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 9/9 | 2815 | chr11 | 113948952 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:113905147
|
G | C | 1 | a0002c0002t0063g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.52+162G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113905147 | ||||||
chr11:113905410
|
T | C | 1 | a0001c0001t0064g0025 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.52+425T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113905410 | ||||||
chr11:113905447
|
C | T | 4 | a0001c0005t0021g0383a0001c0005t0022g0384a0001c0005t0022g0385others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+462C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113905447 | ||||||
chr11:113905476
|
G | A | 1 | a0001c0001t0011g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.52+491G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113905476 | ||||||
chr11:113905981
|
G | A | 1 | a0001c0001t0064g0025 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.52+996G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113905981 | ||||||
chr11:113906237
|
T | G | 1 | a0001c0001t0062g0027 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.52+1252T>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113906237 | ||||||
chr11:113906350
|
G | A | 40 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0032others(37): Show | 40 | HG00741.hp1 HG01081.hp1 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.52+1365G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113906350 | ||||||
chr11:113906584
|
T | A | 1 | a0001c0005t0021g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.52+1599T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113906584 | ||||||
chr11:113906654
|
T | A | 2 | a0001c0001t0053g0069a0003c0004t0025g0070 | 2 | HG00642.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.52+1669T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113906654 | ||||||
chr11:113906958
|
A | G | 1 | a0001c0001t0010g0382 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.52+1973A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113906958 | ||||||
chr11:113907013
|
T | C | 1 | a0001c0003t0003g0071 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.52+2028T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113907013 | ||||||
chr11:113907015
|
C | G | 4 | a0001c0005t0021g0383a0001c0005t0022g0384a0001c0005t0022g0385others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+2030C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113907015 | ||||||
chr11:113907040
|
T | G | 50 | a0001c0001t0011g0113a0001c0003t0003g0004a0001c0003t0003g0007others(47): Show | 57 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.52+2055T>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113907040 | ||||||
chr11:113907113
|
C | A | 6 | a0001c0001t0017g0116a0001c0001t0017g0117a0001c0001t0017g0119others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+2128C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113907113 | ||||||
chr11:113907134
|
T | C | 1 | a0001c0003t0003g0072 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.52+2149T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113907134 | ||||||
chr11:113907342
|
C | T | 1 | a0001c0003t0003g0114 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.53-1953C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113907342 | ||||||
chr11:113907403
|
T | A | 1 | a0001c0001t0005g0028 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.53-1892T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113907403 | ||||||
chr11:113907754
|
C | T | 1 | a0002c0002t0063g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.53-1541C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113907754 | ||||||
chr11:113907828
|
C | T | 1 | a0001c0005t0021g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.53-1467C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113907828 | ||||||
chr11:113907856
|
A | G | 12 | a0001c0001t0004g0003a0001c0001t0004g0372a0001c0001t0004g0373others(9): Show | 14 | HG00597.hp2 HG02015.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.53-1439A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113907856 | ||||||
chr11:113908373
|
G | A | 16 | a0001c0001t0004g0122a0001c0001t0004g0123a0001c0001t0004g0127others(13): Show | 17 | HG01123.hp1 HG01243.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.53-922G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113908373 | ||||||
chr11:113908792
|
C | T | 4 | a0002c0002t0001g0368a0002c0002t0001g0369a0002c0002t0001g0371others(1): Show | 4 | HG02886.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-503C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113908792 | ||||||
chr11:113909067
|
G | A | 1 | a0002c0002t0001g0136 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.53-228G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113909067 | ||||||
chr11:113909102
|
T | C | 4 | a0001c0005t0021g0383a0001c0005t0022g0384a0001c0005t0022g0385others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-193T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113909102 | ||||||
chr11:113909166
|
T | A | 1 | a0002c0002t0006g0137 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.53-129T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113909166 | ||||||
chr11:113909221
|
T | G | 1 | a0001c0001t0002g0138 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.53-74T>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 1/8 | chr11 | 113909221 | ||||||
chr11:113909604
|
A | G | 1 | a0001c0001t0011g0113 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.213+149A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113909604 | ||||||
chr11:113909891
|
G | T | 1 | a0001c0001t0004g0381 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.213+436G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113909891 | ||||||
chr11:113909969
|
T | C | 1 | a0001c0003t0021g0073 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.213+514T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113909969 | ||||||
chr11:113909984
|
C | CA | 106 | a0001c0001t0002g0138a0001c0001t0002g0182a0001c0001t0002g0185others(103): Show | 106 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.213+555dupA | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113909984 | |||||
chr11:113909984
|
C | CAA | 18 | a0001c0001t0005g0029a0001c0001t0005g0032a0001c0001t0005g0034others(15): Show | 18 | HG00323.hp2 HG01255.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.213+554_213+555dup others(2): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113909984 | |||||
chr11:113909984
|
CA | C | 39 | a0001c0001t0002g0367a0001c0003t0003g0004a0001c0003t0003g0009others(36): Show | 44 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.213+555delA | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113909984 | |||||
chr11:113910044
|
A | C | 4 | a0001c0005t0021g0383a0001c0005t0022g0384a0001c0005t0022g0385others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+589A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113910044 | ||||||
chr11:113910154
|
A | G | 1 | a0002c0002t0006g0204 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.213+699A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113910154 | ||||||
chr11:113910259
|
T | C | 4 | a0003c0006t0023g0205a0003c0006t0023g0206a0003c0006t0023g0207others(1): Show | 4 | HG00323.hp2 HG01256.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+804T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113910259 | ||||||
chr11:113910266
|
T | C | 4 | a0001c0005t0021g0383a0001c0005t0022g0384a0001c0005t0022g0385others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+811T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113910266 | ||||||
chr11:113910292
|
A | C | 4 | a0001c0005t0021g0383a0001c0005t0022g0384a0001c0005t0022g0385others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+837A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113910292 | ||||||
chr11:113910442
|
CT | C | 138 | a0001c0001t0002g0015a0001c0001t0002g0138a0001c0001t0002g0229others(135): Show | 149 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.213+1003delT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113910442 | |||||
chr11:113910510
|
G | A | 7 | a0001c0001t0011g0026a0001c0001t0011g0178a0001c0001t0011g0208others(4): Show | 7 | HG02280.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+1055G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113910510 | ||||||
chr11:113910529
|
G | C | 184 | a0001c0001t0002g0015a0001c0001t0002g0138a0001c0001t0002g0229others(181): Show | 202 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.213+1074G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113910529 | ||||||
chr11:113910622
|
G | A | 20 | a0002c0002t0008g0001a0002c0002t0008g0013a0002c0002t0008g0140others(17): Show | 23 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.213+1167G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113910622 | ||||||
chr11:113910630
|
G | A | 4 | a0001c0005t0021g0383a0001c0005t0022g0384a0001c0005t0022g0385others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+1175G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113910630 | ||||||
chr11:113910655
|
G | A | 65 | a0001c0001t0002g0182a0001c0001t0002g0297a0001c0001t0002g0299others(62): Show | 71 | HG00597.hp2 HG00639.hp2 HG01099.hp2 others(68): Show |
intron_variant | MODIFIER | c.213+1200G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113910655 | ||||||
chr11:113910833
|
C | CT | 141 | a0001c0001t0002g0015a0001c0001t0002g0138a0001c0001t0002g0229others(138): Show | 154 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.213+1392dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113910833 | |||||
chr11:113910929
|
A | T | 119 | a0001c0001t0002g0015a0001c0001t0002g0138a0001c0001t0002g0229others(116): Show | 130 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.213+1474A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113910929 | ||||||
chr11:113910976
|
G | A | 4 | a0001c0005t0021g0383a0001c0005t0022g0384a0001c0005t0022g0385others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+1521G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113910976 | ||||||
chr11:113911016
|
T | C | 11 | a0001c0001t0053g0069a0002c0002t0014g0150a0002c0002t0014g0221others(8): Show | 11 | HG00642.hp2 HG00738.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.213+1561T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113911016 | ||||||
chr11:113911293
|
C | T | 1 | a0002c0002t0055g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.213+1838C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113911293 | ||||||
chr11:113911324
|
G | A | 1 | a0001c0005t0021g0383 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.213+1869G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113911324 | ||||||
chr11:113911376
|
A | G | 11 | a0001c0001t0053g0069a0002c0002t0014g0150a0002c0002t0014g0221others(8): Show | 11 | HG00642.hp2 HG00738.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.213+1921A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113911376 | ||||||
chr11:113911417
|
A | G | 184 | a0001c0001t0002g0015a0001c0001t0002g0138a0001c0001t0002g0229others(181): Show | 202 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.213+1962A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113911417 | ||||||
chr11:113911474
|
C | T | 2 | a0002c0002t0020g0145a0002c0002t0020g0203 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.213+2019C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113911474 | ||||||
chr11:113911619
|
C | T | 4 | a0001c0003t0003g0085a0002c0002t0020g0144a0002c0002t0020g0145others(1): Show | 4 | HG02135.hp2 HG03130.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+2164C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113911619 | ||||||
chr11:113911707
|
T | C | 1 | a0002c0002t0001g0227 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.213+2252T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113911707 | ||||||
chr11:113911853
|
T | C | 1 | a0001c0003t0003g0086 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.213+2398T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113911853 | ||||||
chr11:113911866
|
C | T | 1 | a0003c0004t0025g0070 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.213+2411C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113911866 | ||||||
chr11:113912397
|
C | T | 2 | a0002c0002t0020g0145a0002c0002t0020g0203 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.213+2942C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113912397 | ||||||
chr11:113912459
|
G | A | 1 | a0002c0002t0001g0136 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.213+3004G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113912459 | ||||||
chr11:113912464
|
C | T | 2 | a0001c0001t0002g0365a0001c0001t0002g0366 | 2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.213+3009C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113912464 | ||||||
chr11:113912489
|
C | T | 1 | a0001c0001t0005g0067 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.213+3034C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113912489 | ||||||
chr11:113912490
|
G | A | 1 | a0001c0003t0048g0087 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.213+3035G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113912490 | ||||||
chr11:113912514
|
A | T | 1 | a0001c0001t0010g0382 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.213+3059A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113912514 | ||||||
chr11:113913034
|
T | C | 1 | a0002c0002t0001g0309 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.213+3579T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113913034 | ||||||
chr11:113913183
|
A | C | 1 | a0001c0001t0064g0025 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+3728A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113913183 | ||||||
chr11:113913269
|
C | T | 1 | a0001c0005t0021g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.213+3814C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113913269 | ||||||
chr11:113913350
|
A | ATTTTT | 10 | a0002c0002t0001g0261a0002c0002t0001g0263a0002c0002t0001g0264others(7): Show | 10 | HG01256.hp1 HG01952.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.213+3923_213+3927d others(7): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913350
|
A | ATTTTTT | 9 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0265others(6): Show | 13 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.213+3922_213+3927d others(8): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913350
|
A | ATTTTTTT | 11 | a0002c0002t0006g0137a0002c0002t0006g0170a0002c0002t0006g0171others(8): Show | 11 | HG00642.hp1 HG02717.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.213+3921_213+3927d others(9): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913350
|
A | ATTTTTTT others(3): Show |
7 | a0002c0002t0006g0172a0002c0002t0006g0272a0002c0002t0006g0273others(4): Show | 7 | HG01099.hp1 HG01978.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.213+3918_213+3927d others(12): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913350
|
A | ATTTTTTT others(4): Show |
5 | a0002c0002t0006g0173a0002c0002t0006g0174a0002c0002t0006g0175others(2): Show | 5 | HG00423.hp1 HG01496.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+3917_213+3927d others(13): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913350
|
A | ATTTTTTT others(5): Show |
2 | a0002c0002t0014g0225a0003c0004t0025g0152 | 2 | HG00738.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.213+3916_213+3927d others(14): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913350
|
A | ATTTTTTT others(7): Show |
1 | a0002c0002t0014g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.213+3914_213+3927d others(16): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913350
|
AT | A | 118 | a0001c0001t0002g0015a0001c0001t0002g0020a0001c0001t0002g0021others(115): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.213+3927delT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913350
|
ATT | A | 107 | a0001c0001t0002g0138a0001c0001t0002g0182a0001c0001t0002g0185others(104): Show | 116 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.213+3926_213+3927d others(4): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913350
|
ATTT | A | 8 | a0001c0001t0002g0229a0001c0001t0004g0374a0001c0001t0007g0303others(5): Show | 8 | HG01167.hp1 HG03130.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+3925_213+3927d others(5): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913350
|
ATTTTT | A | 19 | a0002c0002t0008g0001a0002c0002t0008g0013a0002c0002t0008g0140others(16): Show | 22 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.213+3923_213+3927d others(7): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913350
|
ATTTTTTT others(3): Show |
A | 3 | a0001c0003t0003g0083a0001c0003t0003g0084a0002c0002t0001g0228 | 3 | HG02129.hp1 NA18981.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.213+3918_213+3927d others(12): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913350
|
ATTTTTTT others(4): Show |
A | 45 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(42): Show | 51 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.213+3917_213+3927d others(13): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913350
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0011g0113 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.213+3914_213+3927d others(16): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113913350 | |||||
chr11:113913453
|
C | T | 2 | a0001c0001t0011g0283a0001c0001t0011g0284 | 2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.213+3998C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113913453 | ||||||
chr11:113913454
|
G | A | 1 | a0001c0005t0021g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.213+3999G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113913454 | ||||||
chr11:113913543
|
C | A | 4 | a0004c0007t0019g0313a0004c0007t0019g0314a0004c0007t0019g0315others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+4088C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113913543 | ||||||
chr11:113913655
|
C | T | 3 | a0002c0002t0001g0253a0002c0002t0001g0254a0002c0002t0001g0255 | 3 | NA19066.hp2 NA19070.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.213+4200C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113913655 | ||||||
chr11:113913989
|
C | T | 1 | a0001c0001t0005g0187 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.213+4534C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113913989 | ||||||
chr11:113914043
|
AT | A | 8 | a0001c0001t0007g0126a0001c0001t0007g0286a0001c0001t0011g0026others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+4602delT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113914043 | |||||
chr11:113914044
|
T | TA | 38 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0032others(35): Show | 38 | HG00741.hp1 HG01081.hp1 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.213+4589_213+4590i others(3): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914044 | ||||||
chr11:113914045
|
T | A | 163 | a0001c0001t0002g0015a0001c0001t0002g0138a0001c0001t0002g0188others(160): Show | 178 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.213+4590T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914045 | ||||||
chr11:113914046
|
T | A | 38 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0032others(35): Show | 38 | HG00741.hp1 HG01081.hp1 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.213+4591T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914046 | ||||||
chr11:113914047
|
T | A | 23 | a0001c0001t0005g0187a0001c0001t0053g0069a0001c0003t0003g0075others(20): Show | 24 | HG00323.hp2 HG00423.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.213+4592T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914047 | ||||||
chr11:113914048
|
T | A | 37 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0032others(34): Show | 37 | HG00741.hp1 HG01081.hp1 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.213+4593T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914048 | ||||||
chr11:113914152
|
G | T | 1 | a0001c0003t0003g0082 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.213+4697G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914152 | ||||||
chr11:113914157
|
A | T | 1 | a0002c0002t0006g0260 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.213+4702A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914157 | ||||||
chr11:113914194
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.213+4739G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914194 | ||||||
chr11:113914234
|
G | A | 110 | a0001c0001t0002g0015a0001c0001t0002g0138a0001c0001t0002g0229others(107): Show | 122 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.213+4779G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914234 | ||||||
chr11:113914382
|
T | C | 1 | a0001c0001t0037g0161 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.213+4927T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914382 | ||||||
chr11:113914450
|
G | C | 1 | a0001c0003t0003g0090 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.213+4995G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914450 | ||||||
chr11:113914464
|
C | CA | 11 | a0001c0001t0053g0069a0002c0002t0014g0150a0002c0002t0014g0221others(8): Show | 11 | HG00642.hp2 HG00738.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.213+5021dupA | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113914464 | |||||
chr11:113914547
|
A | G | 38 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0032others(35): Show | 38 | HG00741.hp1 HG01081.hp1 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.213+5092A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914547 | ||||||
chr11:113914553
|
C | G | 1 | a0001c0001t0009g0356 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.213+5098C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914553 | ||||||
chr11:113914620
|
T | G | 1 | a0001c0001t0004g0304 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.213+5165T>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914620 | ||||||
chr11:113914704
|
C | T | 7 | a0001c0001t0011g0026a0001c0001t0011g0178a0001c0001t0011g0208others(4): Show | 7 | HG02280.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+5249C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914704 | ||||||
chr11:113914749
|
T | C | 1 | a0001c0001t0005g0037 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.213+5294T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113914749 | ||||||
chr11:113915055
|
A | G | 1 | a0002c0002t0014g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.213+5600A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113915055 | ||||||
chr11:113915194
|
G | T | 29 | a0001c0001t0057g0167a0002c0002t0001g0168a0002c0002t0001g0169others(26): Show | 33 | HG00423.hp1 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.213+5739G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113915194 | ||||||
chr11:113915195
|
T | TTTGTTTG | 47 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(44): Show | 53 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.213+5743_213+5749d others(9): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113915195 | |||||
chr11:113915236
|
C | T | 1 | a0002c0002t0024g0259 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.213+5781C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113915236 | ||||||
chr11:113915290
|
A | G | 1 | a0001c0001t0064g0025 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.213+5835A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113915290 | ||||||
chr11:113915318
|
A | C | 1 | a0002c0002t0015g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.213+5863A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113915318 | ||||||
chr11:113915665
|
C | T | 2 | a0001c0001t0002g0354a0001c0001t0002g0355 | 2 | HG01255.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.213+6210C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113915665 | ||||||
chr11:113915817
|
C | T | 233 | a0001c0001t0002g0015a0001c0001t0002g0138a0001c0001t0002g0229others(230): Show | 251 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.213+6362C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113915817 | ||||||
chr11:113915846
|
G | GT | 7 | a0001c0001t0005g0035a0001c0001t0041g0134a0001c0003t0003g0090others(4): Show | 7 | HG00323.hp2 HG01256.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.213+6401dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113915846 | |||||
chr11:113915856
|
T | C | 4 | a0001c0005t0021g0383a0001c0005t0022g0384a0001c0005t0022g0385others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+6401T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113915856 | ||||||
chr11:113915993
|
C | T | 2 | a0001c0001t0002g0279a0001c0001t0002g0280 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.213+6538C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113915993 | ||||||
chr11:113916033
|
C | T | 1 | a0002c0002t0001g0258 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.213+6578C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113916033 | ||||||
chr11:113916196
|
A | T | 14 | a0001c0003t0003g0008a0001c0003t0003g0010a0001c0003t0003g0075others(11): Show | 16 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.213+6741A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113916196 | ||||||
chr11:113916487
|
T | C | 52 | a0001c0001t0011g0113a0001c0003t0003g0004a0001c0003t0003g0007others(49): Show | 58 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.213+7032T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113916487 | ||||||
chr11:113916625
|
T | C | 12 | a0002c0002t0008g0001a0002c0002t0008g0013a0002c0002t0008g0140others(9): Show | 15 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.213+7170T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113916625 | ||||||
chr11:113916723
|
A | G | 1 | a0001c0003t0003g0080 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.213+7268A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113916723 | ||||||
chr11:113916749
|
C | A | 2 | a0001c0001t0002g0320a0001c0001t0002g0321 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.213+7294C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113916749 | ||||||
chr11:113917135
|
A | AT | 17 | a0001c0001t0002g0182a0001c0001t0002g0297a0001c0001t0002g0299others(14): Show | 17 | HG02129.hp1 NA18522.hp2 NA18939.hp2 others(14): Show |
intron_variant | MODIFIER | c.213+7694dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113917135 | |||||
chr11:113917135
|
A | ATT | 106 | a0001c0001t0002g0015a0001c0001t0002g0138a0001c0001t0002g0229others(103): Show | 118 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.213+7693_213+7694d others(4): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113917135 | |||||
chr11:113917173
|
C | T | 3 | a0001c0005t0022g0384a0001c0005t0022g0385a0001c0005t0022g0386 | 3 | HG01891.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.213+7718C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113917173 | ||||||
chr11:113917279
|
C | A | 10 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(7): Show | 10 | HG00738.hp1 HG01099.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.213+7824C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113917279 | ||||||
chr11:113917323
|
G | T | 1 | a0001c0001t0053g0069 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.213+7868G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113917323 | ||||||
chr11:113917554
|
T | C | 1 | a0001c0005t0022g0384 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.213+8099T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113917554 | ||||||
chr11:113917588
|
A | G | 1 | a0001c0001t0009g0199 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.213+8133A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113917588 | ||||||
chr11:113917620
|
G | GT | 6 | a0001c0001t0002g0202a0001c0001t0005g0057a0001c0001t0005g0066others(3): Show | 6 | HG02055.hp1 HG02080.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+8173dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113917620 | |||||
chr11:113917701
|
C | T | 7 | a0001c0001t0011g0026a0001c0001t0011g0178a0001c0001t0011g0208others(4): Show | 7 | HG02280.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+8246C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113917701 | ||||||
chr11:113917721
|
C | T | 22 | a0002c0002t0008g0001a0002c0002t0008g0013a0002c0002t0008g0140others(19): Show | 25 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.213+8266C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113917721 | ||||||
chr11:113917804
|
C | T | 3 | a0003c0004t0025g0151a0003c0004t0025g0152a0003c0004t0061g0141 | 3 | HG02723.hp2 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.213+8349C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113917804 | ||||||
chr11:113917824
|
C | T | 10 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(7): Show | 10 | HG00738.hp1 HG01099.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.213+8369C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113917824 | ||||||
chr11:113917940
|
T | C | 1 | a0001c0001t0002g0322 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.213+8485T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113917940 | ||||||
chr11:113918080
|
T | C | 3 | a0001c0001t0002g0323a0001c0001t0010g0019a0001c0001t0010g0324 | 4 | HG00140.hp2 HG01081.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+8625T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113918080 | ||||||
chr11:113918267
|
T | A | 47 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(44): Show | 53 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.213+8812T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113918267 | ||||||
chr11:113918268
|
C | CGT | 188 | a0001c0001t0002g0182a0001c0001t0002g0297a0001c0001t0002g0299others(185): Show | 204 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(201): Show |
intron_variant | MODIFIER | c.213+8840_213+8841d others(4): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113918268 | |||||
chr11:113918268
|
C | CGTCTGTG others(3): Show |
2 | a0001c0003t0003g0091a0001c0003t0003g0092 | 2 | NA18948.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.213+8815_213+8816i others(12): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113918268 | |||||
chr11:113918268
|
C | CGTGT | 61 | a0001c0001t0004g0017a0001c0001t0004g0293a0001c0001t0005g0028others(58): Show | 62 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.213+8838_213+8841d others(6): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113918268 | |||||
chr11:113918268
|
C | CGTGTGT | 52 | a0001c0001t0011g0026a0001c0001t0011g0178a0001c0001t0011g0208others(49): Show | 58 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.213+8836_213+8841d others(8): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113918268 | |||||
chr11:113918268
|
C | CGTGTGTG others(1): Show |
7 | a0001c0003t0003g0098a0001c0003t0003g0099a0002c0002t0014g0150others(4): Show | 7 | HG00621.hp1 HG00738.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+8834_213+8841d others(10): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113918268 | |||||
chr11:113918268
|
C | CGTGTGTG others(3): Show |
6 | a0001c0003t0003g0077a0001c0003t0003g0078a0001c0003t0003g0079others(3): Show | 6 | HG01192.hp2 HG01952.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+8832_213+8841d others(12): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113918268 | |||||
chr11:113918426
|
A | C | 13 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(10): Show | 13 | HG00738.hp1 HG01099.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.213+8971A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113918426 | ||||||
chr11:113918539
|
G | A | 4 | a0003c0006t0023g0205a0003c0006t0023g0206a0003c0006t0023g0207others(1): Show | 4 | HG00323.hp2 HG01256.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+9084G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113918539 | ||||||
chr11:113918570
|
T | A | 110 | a0001c0001t0057g0167a0002c0002t0001g0005a0002c0002t0001g0014others(107): Show | 121 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.213+9115T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113918570 | ||||||
chr11:113918577
|
G | A | 127 | a0001c0001t0057g0167a0002c0002t0001g0005a0002c0002t0001g0014others(124): Show | 138 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.213+9122G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113918577 | ||||||
chr11:113918625
|
C | CT | 115 | a0001c0001t0005g0056a0001c0001t0017g0116a0001c0001t0017g0117others(112): Show | 125 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.213+9184dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113918625 | |||||
chr11:113918658
|
A | G | 110 | a0001c0001t0057g0167a0002c0002t0001g0005a0002c0002t0001g0014others(107): Show | 121 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.213+9203A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113918658 | ||||||
chr11:113918662
|
A | AT | 111 | a0001c0001t0004g0374a0001c0001t0057g0167a0002c0002t0001g0005others(108): Show | 122 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.213+9218dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113918662 | |||||
chr11:113918744
|
C | T | 1 | a0001c0005t0022g0385 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.213+9289C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113918744 | ||||||
chr11:113918839
|
T | G | 1 | a0001c0001t0002g0325 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.213+9384T>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113918839 | ||||||
chr11:113918867
|
G | A | 3 | a0002c0002t0020g0144a0002c0002t0020g0145a0002c0002t0020g0203 | 3 | HG03130.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.213+9412G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113918867 | ||||||
chr11:113919294
|
G | A | 1 | a0001c0003t0003g0075 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.213+9839G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113919294 | ||||||
chr11:113919377
|
C | T | 110 | a0001c0001t0057g0167a0002c0002t0001g0005a0002c0002t0001g0014others(107): Show | 121 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.213+9922C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113919377 | ||||||
chr11:113919401
|
A | G | 1 | a0002c0002t0006g0260 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.213+9946A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113919401 | ||||||
chr11:113919518
|
T | A | 110 | a0001c0001t0057g0167a0002c0002t0001g0005a0002c0002t0001g0014others(107): Show | 121 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.213+10063T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113919518 | ||||||
chr11:113919554
|
C | T | 1 | a0001c0001t0005g0187 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.213+10099C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113919554 | ||||||
chr11:113919723
|
G | A | 1 | a0001c0003t0003g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.213+10268G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113919723 | ||||||
chr11:113919828
|
C | G | 1 | a0001c0001t0016g0285 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.213+10373C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113919828 | ||||||
chr11:113919829
|
A | C | 1 | a0001c0001t0016g0285 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.213+10374A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113919829 | ||||||
chr11:113919830
|
A | AAAC | 44 | a0001c0001t0002g0344a0001c0001t0004g0122a0001c0001t0004g0123others(41): Show | 47 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.213+10411_213+1041 others(7): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113919830 | |||||
chr11:113919830
|
A | AAACAAC | 4 | a0001c0001t0005g0028a0001c0001t0007g0132a0001c0005t0021g0383others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+10408_213+1041 others(10): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113919830 | |||||
chr11:113919830
|
AAAC | A | 15 | a0002c0002t0001g0168a0002c0002t0001g0263a0002c0002t0014g0150others(12): Show | 15 | HG00738.hp1 HG01099.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.213+10411_213+1041 others(7): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113919830 | |||||
chr11:113919879
|
A | C | 4 | a0001c0005t0021g0383a0001c0005t0022g0384a0001c0005t0022g0385others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+10424A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113919879 | ||||||
chr11:113919946
|
A | G | 110 | a0001c0001t0057g0167a0002c0002t0001g0005a0002c0002t0001g0014others(107): Show | 121 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.213+10491A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113919946 | ||||||
chr11:113920019
|
A | AT | 13 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(10): Show | 13 | HG00738.hp1 HG01099.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.213+10569dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113920019 | |||||
chr11:113920255
|
G | A | 47 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(44): Show | 53 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.213+10800G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113920255 | ||||||
chr11:113920303
|
C | T | 1 | a0001c0001t0005g0187 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.213+10848C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113920303 | ||||||
chr11:113920317
|
C | T | 1 | a0002c0002t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.213+10862C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113920317 | ||||||
chr11:113920387
|
G | GT | 111 | a0001c0001t0057g0167a0002c0002t0001g0005a0002c0002t0001g0014others(108): Show | 122 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.213+10938dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113920387 | |||||
chr11:113920390
|
T | TG | 3 | a0002c0002t0001g0168a0002c0002t0001g0263a0002c0002t0001g0266 | 3 | HG02572.hp1 HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.213+10935_213+1093 others(5): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113920390 | ||||||
chr11:113920478
|
C | T | 1 | a0001c0001t0060g0195 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214-10906C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113920478 | ||||||
chr11:113920556
|
T | A | 88 | a0001c0001t0057g0167a0002c0002t0001g0005a0002c0002t0001g0014others(85): Show | 96 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.214-10828T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113920556 | ||||||
chr11:113920562
|
C | T | 1 | a0001c0001t0005g0028 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.214-10822C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113920562 | ||||||
chr11:113920691
|
C | A | 21 | a0002c0002t0006g0002a0002c0002t0006g0011a0002c0002t0006g0112others(18): Show | 25 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.214-10693C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113920691 | ||||||
chr11:113920994
|
G | C | 110 | a0001c0001t0057g0167a0002c0002t0001g0005a0002c0002t0001g0014others(107): Show | 121 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.214-10390G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113920994 | ||||||
chr11:113921024
|
G | A | 1 | a0001c0001t0002g0323 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.214-10360G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921024 | ||||||
chr11:113921045
|
G | A | 4 | a0003c0006t0023g0205a0003c0006t0023g0206a0003c0006t0023g0207others(1): Show | 4 | HG00323.hp2 HG01256.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-10339G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921045 | ||||||
chr11:113921104
|
C | A | 51 | a0002c0002t0001g0005a0002c0002t0001g0014a0002c0002t0001g0016others(48): Show | 55 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.214-10280C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921104 | ||||||
chr11:113921105
|
G | A | 37 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0032others(34): Show | 37 | HG00741.hp1 HG01081.hp1 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.214-10279G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921105 | ||||||
chr11:113921154
|
AT | A | 88 | a0001c0001t0057g0167a0002c0002t0001g0005a0002c0002t0001g0014others(85): Show | 96 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.214-10220delT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113921154 | |||||
chr11:113921177
|
C | T | 47 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(44): Show | 53 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.214-10207C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921177 | ||||||
chr11:113921211
|
T | C | 8 | a0002c0002t0012g0133a0002c0002t0012g0148a0002c0002t0012g0216others(5): Show | 8 | HG01109.hp2 HG02145.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-10173T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921211 | ||||||
chr11:113921232
|
G | A | 1 | a0001c0008t0002g0326 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.214-10152G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921232 | ||||||
chr11:113921303
|
G | A | 3 | a0002c0002t0024g0259a0002c0002t0024g0268a0002c0002t0024g0269 | 3 | HG02735.hp1 HG03017.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.214-10081G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921303 | ||||||
chr11:113921448
|
C | T | 1 | a0001c0001t0011g0113 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.214-9936C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921448 | ||||||
chr11:113921461
|
A | T | 4 | a0004c0007t0019g0313a0004c0007t0019g0314a0004c0007t0019g0315others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-9923A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921461 | ||||||
chr11:113921511
|
T | TACTC | 180 | a0001c0001t0011g0113a0001c0001t0053g0069a0001c0001t0057g0167others(177): Show | 197 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.214-9873_214-9872i others(6): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921511 | ||||||
chr11:113921613
|
G | T | 47 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(44): Show | 53 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.214-9771G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921613 | ||||||
chr11:113921617
|
C | CA | 13 | a0001c0001t0002g0138a0001c0001t0002g0322a0001c0001t0007g0179others(10): Show | 13 | HG01891.hp2 HG02129.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.214-9751dupA | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113921617 | |||||
chr11:113921617
|
CA | C | 19 | a0001c0001t0002g0342a0001c0001t0005g0055a0001c0001t0007g0143others(16): Show | 19 | HG00323.hp2 HG01109.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.214-9751delA | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113921617 | |||||
chr11:113921642
|
G | C | 1 | a0001c0003t0003g0094 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.214-9742G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921642 | ||||||
chr11:113921688
|
G | C | 3 | a0002c0002t0020g0144a0002c0002t0020g0145a0002c0002t0020g0203 | 3 | HG03130.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.214-9696G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921688 | ||||||
chr11:113921725
|
C | A | 7 | a0002c0002t0001g0014a0002c0002t0001g0016a0002c0002t0001g0155others(4): Show | 9 | HG00558.hp1 HG00597.hp1 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.214-9659C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921725 | ||||||
chr11:113921828
|
A | G | 8 | a0002c0002t0012g0133a0002c0002t0012g0148a0002c0002t0012g0216others(5): Show | 8 | HG01109.hp2 HG02145.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-9556A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921828 | ||||||
chr11:113921922
|
C | T | 22 | a0002c0002t0008g0001a0002c0002t0008g0013a0002c0002t0008g0140others(19): Show | 25 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.214-9462C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921922 | ||||||
chr11:113921950
|
T | C | 22 | a0002c0002t0008g0001a0002c0002t0008g0013a0002c0002t0008g0140others(19): Show | 25 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.214-9434T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113921950 | ||||||
chr11:113922125
|
C | A | 6 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(3): Show | 6 | HG01884.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-9259C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922125 | ||||||
chr11:113922149
|
T | A | 1 | a0002c0002t0024g0259 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.214-9235T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922149 | ||||||
chr11:113922175
|
C | A | 4 | a0004c0007t0019g0313a0004c0007t0019g0314a0004c0007t0019g0315others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-9209C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922175 | ||||||
chr11:113922206
|
C | A | 1 | a0001c0001t0005g0187 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214-9178C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922206 | ||||||
chr11:113922234
|
T | TTTTA | 6 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(3): Show | 6 | HG01884.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-9130_214-9127d others(6): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113922234 | |||||
chr11:113922283
|
A | G | 10 | a0001c0001t0053g0069a0002c0002t0014g0150a0002c0002t0014g0221others(7): Show | 10 | HG00642.hp2 HG00738.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.214-9101A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922283 | ||||||
chr11:113922300
|
C | T | 6 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(3): Show | 6 | HG01884.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-9084C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922300 | ||||||
chr11:113922423
|
T | G | 3 | a0001c0001t0002g0185a0001c0001t0002g0365a0001c0001t0002g0366 | 3 | HG00639.hp1 HG01074.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.214-8961T>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922423 | ||||||
chr11:113922455
|
A | G | 4 | a0002c0002t0015g0159a0002c0002t0015g0160a0002c0002t0015g0249others(1): Show | 4 | NA19058.hp2 NA19060.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-8929A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922455 | ||||||
chr11:113922546
|
T | C | 2 | a0001c0001t0002g0189a0001c0001t0002g0310 | 2 | HG00673.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.214-8838T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922546 | ||||||
chr11:113922549
|
T | TTTTA | 52 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(49): Show | 58 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.214-8823_214-8820d others(6): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113922549 | |||||
chr11:113922594
|
C | T | 5 | a0001c0005t0021g0068a0001c0005t0021g0383a0001c0005t0022g0384others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-8790C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922594 | ||||||
chr11:113922637
|
G | C | 1 | a0001c0003t0049g0088 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.214-8747G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922637 | ||||||
chr11:113922705
|
G | A | 1 | a0001c0003t0003g0098 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.214-8679G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922705 | ||||||
chr11:113922765
|
C | T | 52 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(49): Show | 58 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.214-8619C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922765 | ||||||
chr11:113922969
|
A | G | 1 | a0001c0003t0003g0110 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.214-8415A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113922969 | ||||||
chr11:113923206
|
A | G | 4 | a0003c0006t0023g0205a0003c0006t0023g0206a0003c0006t0023g0207others(1): Show | 4 | HG00323.hp2 HG01256.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-8178A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113923206 | ||||||
chr11:113923303
|
C | T | 1 | a0001c0001t0005g0187 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214-8081C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113923303 | ||||||
chr11:113923480
|
C | G | 1 | a0001c0001t0002g0341 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.214-7904C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113923480 | ||||||
chr11:113923669
|
T | C | 1 | a0002c0002t0001g0231 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.214-7715T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113923669 | ||||||
chr11:113923722
|
G | A | 1 | a0002c0002t0001g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.214-7662G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113923722 | ||||||
chr11:113923755
|
C | T | 14 | a0001c0003t0003g0008a0001c0003t0003g0010a0001c0003t0003g0075others(11): Show | 16 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.214-7629C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113923755 | ||||||
chr11:113923764
|
A | G | 1 | a0002c0002t0001g0162 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.214-7620A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113923764 | ||||||
chr11:113923765
|
C | A | 1 | a0002c0002t0001g0162 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.214-7619C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113923765 | ||||||
chr11:113923984
|
C | T | 1 | a0001c0005t0022g0386 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.214-7400C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113923984 | ||||||
chr11:113923986
|
A | T | 1 | a0001c0005t0022g0386 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.214-7398A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113923986 | ||||||
chr11:113924159
|
A | AGCATAGT others(8): Show |
1 | a0003c0006t0023g0207 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.214-7224_214-7210d others(17): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113924159 | |||||
chr11:113924302
|
A | T | 1 | a0003c0006t0023g0205 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214-7082A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113924302 | ||||||
chr11:113924372
|
T | C | 1 | a0001c0001t0002g0327 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.214-7012T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113924372 | ||||||
chr11:113924431
|
C | G | 3 | a0001c0001t0010g0194a0001c0001t0010g0339a0001c0001t0010g0340 | 3 | HG00323.hp1 HG00741.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.214-6953C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113924431 | ||||||
chr11:113924502
|
C | G | 62 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(59): Show | 68 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.214-6882C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113924502 | ||||||
chr11:113924624
|
C | CA | 131 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0138others(128): Show | 139 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.214-6737dupA | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113924624 | |||||
chr11:113924624
|
C | CAA | 165 | a0001c0001t0002g0015a0001c0001t0002g0020a0001c0001t0002g0202others(162): Show | 181 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.214-6738_214-6737d others(4): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113924624 | |||||
chr11:113924624
|
C | CAAA | 57 | a0001c0001t0004g0373a0001c0001t0005g0028a0001c0001t0005g0034others(54): Show | 58 | HG00323.hp2 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.214-6739_214-6737d others(5): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113924624 | |||||
chr11:113924652
|
A | G | 1 | a0001c0001t0017g0116 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.214-6732A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113924652 | ||||||
chr11:113924689
|
C | A | 9 | a0001c0001t0005g0029a0001c0001t0005g0037a0001c0001t0005g0041others(6): Show | 9 | HG02083.hp2 NA18939.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.214-6695C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113924689 | ||||||
chr11:113924714
|
C | T | 1 | a0003c0004t0025g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.214-6670C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113924714 | ||||||
chr11:113924874
|
T | G | 21 | a0002c0002t0008g0001a0002c0002t0008g0013a0002c0002t0008g0140others(18): Show | 24 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.214-6510T>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113924874 | ||||||
chr11:113924905
|
A | C | 1 | a0002c0002t0001g0162 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.214-6479A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113924905 | ||||||
chr11:113925239
|
G | A | 5 | a0001c0001t0004g0305a0003c0006t0023g0205a0003c0006t0023g0206others(2): Show | 5 | HG00323.hp2 HG01256.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-6145G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113925239 | ||||||
chr11:113925362
|
T | C | 6 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(3): Show | 6 | HG01884.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-6022T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113925362 | ||||||
chr11:113925411
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.214-5973G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113925411 | ||||||
chr11:113925417
|
G | GT | 74 | a0001c0001t0002g0138a0001c0001t0002g0200a0001c0001t0002g0201others(71): Show | 74 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.214-5943dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113925417 | |||||
chr11:113925417
|
GT | G | 10 | a0001c0001t0007g0287a0002c0002t0014g0150a0002c0002t0014g0224others(7): Show | 11 | HG00738.hp1 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.214-5943delT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113925417 | |||||
chr11:113925417
|
GTTTTTTT others(2): Show |
G | 45 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(42): Show | 51 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.214-5951_214-5943d others(11): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113925417 | |||||
chr11:113925417
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0011g0113 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.214-5953_214-5943d others(13): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113925417 | |||||
chr11:113925468
|
G | T | 11 | a0001c0003t0003g0008a0001c0003t0003g0010a0001c0003t0003g0075others(8): Show | 13 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.214-5916G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113925468 | ||||||
chr11:113925526
|
C | T | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-5858C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113925526 | ||||||
chr11:113925546
|
C | T | 1 | a0003c0006t0023g0205 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214-5838C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113925546 | ||||||
chr11:113925579
|
A | T | 1 | a0003c0006t0023g0205 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214-5805A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113925579 | ||||||
chr11:113925591
|
T | A | 1 | a0002c0002t0006g0002 | 4 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-5793T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113925591 | ||||||
chr11:113925896
|
C | A | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-5488C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113925896 | ||||||
chr11:113925900
|
A | C | 1 | a0001c0001t0004g0372 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.214-5484A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113925900 | ||||||
chr11:113925929
|
A | C | 1 | a0003c0006t0023g0205 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214-5455A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113925929 | ||||||
chr11:113926225
|
G | C | 1 | a0001c0001t0002g0360 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.214-5159G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113926225 | ||||||
chr11:113926339
|
T | C | 1 | a0001c0003t0003g0101 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.214-5045T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113926339 | ||||||
chr11:113926424
|
T | C | 46 | a0002c0002t0008g0001a0002c0002t0008g0013a0002c0002t0008g0140others(43): Show | 50 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.214-4960T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113926424 | ||||||
chr11:113926448
|
T | TTTTCC | 3 | a0001c0001t0027g0312a0002c0002t0014g0150a0002c0002t0014g0221 | 3 | HG01070.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.214-4921_214-4917d others(7): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926448 | |||||
chr11:113926448
|
T | TTTTCCTT others(3): Show |
4 | a0002c0002t0014g0224a0002c0002t0014g0225a0002c0002t0014g0226others(1): Show | 4 | HG00738.hp1 HG01099.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-4926_214-4917d others(12): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926448 | |||||
chr11:113926448
|
T | TTTTCCTT others(13): Show |
1 | a0001c0001t0005g0035 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.214-4917_214-4916i others(22): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926448 | |||||
chr11:113926448
|
TTTTCCTT others(33): Show |
T | 2 | a0002c0002t0020g0144a0002c0002t0028g0012 | 3 | HG02109.hp2 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.214-4916_214-4877d others(42): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926448 | |||||
chr11:113926468
|
T | C | 9 | a0001c0001t0005g0035a0001c0001t0027g0312a0002c0002t0014g0150others(6): Show | 9 | HG00738.hp1 HG01070.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.214-4916T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113926468 | ||||||
chr11:113926468
|
T | TTTTCC | 105 | a0001c0001t0002g0015a0001c0001t0002g0021a0001c0001t0002g0138others(102): Show | 120 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.214-4852_214-4848d others(7): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
T | TTTTCCTT others(3): Show |
47 | a0001c0001t0002g0279a0001c0001t0002g0317a0001c0001t0002g0323others(44): Show | 48 | HG00544.hp1 HG00621.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.214-4857_214-4848d others(12): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
T | TTTTCCTT others(8): Show |
18 | a0001c0001t0005g0040a0001c0001t0005g0053a0001c0001t0007g0130others(15): Show | 18 | HG01167.hp2 HG01981.hp1 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.214-4862_214-4848d others(17): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
T | TTTTCCTT others(13): Show |
10 | a0001c0001t0004g0127a0001c0001t0004g0128a0001c0001t0005g0049others(7): Show | 11 | HG00673.hp2 HG02258.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.214-4867_214-4848d others(22): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
T | TTTTCCTT others(18): Show |
16 | a0001c0001t0004g0122a0001c0001t0005g0028a0001c0001t0005g0042others(13): Show | 16 | HG01081.hp1 HG01123.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.214-4872_214-4848d others(27): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
T | TTTTCCTT others(23): Show |
10 | a0001c0001t0005g0029a0001c0001t0005g0055a0001c0001t0005g0063others(7): Show | 10 | HG00741.hp1 HG01891.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-4877_214-4848d others(32): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
T | TTTTCCTT others(28): Show |
16 | a0001c0001t0004g0123a0001c0001t0005g0032a0001c0001t0005g0041others(13): Show | 16 | HG00323.hp2 HG01346.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.214-4882_214-4848d others(37): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
T | TTTTCCTT others(33): Show |
5 | a0001c0001t0005g0034a0001c0001t0005g0037a0001c0001t0031g0045others(2): Show | 5 | HG01884.hp1 HG01928.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-4887_214-4848d others(42): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
T | TTTTCCTT others(38): Show |
2 | a0001c0001t0005g0044a0001c0001t0005g0062 | 2 | NA18954.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.214-4892_214-4848d others(47): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
T | TTTTCCTT others(43): Show |
1 | a0001c0001t0005g0039 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.214-4897_214-4848d others(52): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
T | TTTTCCTT others(48): Show |
1 | a0001c0003t0003g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.214-4902_214-4848d others(57): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
T | TTTTCCTT others(63): Show |
1 | a0003c0006t0023g0206 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.214-4848_214-4847i others(72): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
T | TTTTCCTT others(122): Show |
1 | a0003c0006t0023g0207 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.214-4848_214-4847i others(131): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
TTTTCC | T | 46 | a0001c0001t0002g0299a0001c0001t0002g0327a0001c0001t0002g0337others(43): Show | 51 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.214-4852_214-4848d others(7): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
TTTTCCTT others(3): Show |
T | 12 | a0001c0001t0002g0320a0001c0001t0002g0321a0001c0001t0004g0003others(9): Show | 14 | HG02895.hp2 HG02897.hp1 HG03704.hp2 others(11): Show |
intron_variant | MODIFIER | c.214-4857_214-4848d others(12): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926468
|
TTTTCCTT others(8): Show |
T | 5 | a0001c0005t0021g0068a0001c0005t0022g0384a0001c0005t0022g0385others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-4862_214-4848d others(17): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926468 | |||||
chr11:113926482
|
C | CCTTTCCT others(32): Show |
1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-4900_214-4862d others(41): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926482 | |||||
chr11:113926483
|
C | T | 1 | a0001c0001t0039g0357 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.214-4901C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113926483 | ||||||
chr11:113926488
|
C | T | 1 | a0001c0001t0002g0341 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.214-4896C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113926488 | ||||||
chr11:113926517
|
C | CCTTTCCT others(12): Show |
1 | a0002c0002t0006g0204 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.214-4866_214-4848d others(21): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926517 | |||||
chr11:113926517
|
C | CCTTTCCT others(13): Show |
1 | a0002c0002t0006g0171 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.214-4866_214-4847d others(22): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926517 | |||||
chr11:113926531
|
T | TCTTCCTT others(113): Show |
1 | a0003c0006t0023g0205 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214-4852_214-4851i others(122): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113926531 | |||||
chr11:113926533
|
C | T | 1 | a0003c0006t0023g0205 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214-4851C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113926533 | ||||||
chr11:113926716
|
C | A | 1 | a0001c0001t0062g0027 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.214-4668C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113926716 | ||||||
chr11:113926721
|
G | A | 1 | a0005c0009t0017g0318 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.214-4663G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113926721 | ||||||
chr11:113926746
|
C | T | 1 | a0001c0001t0002g0336 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.214-4638C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113926746 | ||||||
chr11:113926809
|
G | A | 1 | a0001c0005t0021g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.214-4575G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113926809 | ||||||
chr11:113926847
|
G | C | 1 | a0001c0005t0021g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.214-4537G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113926847 | ||||||
chr11:113927174
|
A | G | 6 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(3): Show | 6 | HG01884.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-4210A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113927174 | ||||||
chr11:113927436
|
A | G | 1 | a0001c0001t0010g0324 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.214-3948A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113927436 | ||||||
chr11:113927479
|
G | A | 1 | a0001c0001t0005g0047 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.214-3905G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113927479 | ||||||
chr11:113927479
|
G | C | 4 | a0004c0007t0019g0313a0004c0007t0019g0314a0004c0007t0019g0315others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-3905G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113927479 | ||||||
chr11:113927593
|
C | T | 1 | a0001c0001t0060g0195 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214-3791C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113927593 | ||||||
chr11:113927612
|
G | C | 2 | a0001c0001t0026g0115a0001c0001t0026g0118 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.214-3772G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113927612 | ||||||
chr11:113927615
|
A | G | 1 | a0001c0003t0003g0109 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.214-3769A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113927615 | ||||||
chr11:113927710
|
G | A | 1 | a0001c0001t0005g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.214-3674G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113927710 | ||||||
chr11:113927723
|
C | T | 5 | a0001c0001t0007g0129a0004c0007t0019g0313a0004c0007t0019g0314others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-3661C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113927723 | ||||||
chr11:113928041
|
C | G | 1 | a0001c0001t0005g0187 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214-3343C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928041 | ||||||
chr11:113928112
|
T | A | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-3272T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928112 | ||||||
chr11:113928113
|
T | C | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-3271T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928113 | ||||||
chr11:113928115
|
T | C | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-3269T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928115 | ||||||
chr11:113928116
|
G | T | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-3268G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928116 | ||||||
chr11:113928119
|
T | A | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-3265T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928119 | ||||||
chr11:113928120
|
G | T | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-3264G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928120 | ||||||
chr11:113928121
|
A | C | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-3263A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928121 | ||||||
chr11:113928123
|
A | G | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-3261A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928123 | ||||||
chr11:113928124
|
A | T | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-3260A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928124 | ||||||
chr11:113928125
|
C | T | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-3259C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928125 | ||||||
chr11:113928156
|
A | G | 3 | a0001c0001t0002g0279a0001c0001t0002g0280a0001c0001t0050g0177 | 3 | HG03834.hp1 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.214-3228A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928156 | ||||||
chr11:113928201
|
A | G | 7 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(4): Show | 7 | HG00738.hp1 HG01099.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-3183A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928201 | ||||||
chr11:113928325
|
G | C | 91 | a0001c0001t0057g0167a0002c0002t0001g0005a0002c0002t0001g0014others(88): Show | 99 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.214-3059G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928325 | ||||||
chr11:113928344
|
T | C | 1 | a0005c0009t0017g0318 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.214-3040T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928344 | ||||||
chr11:113928366
|
T | C | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-3018T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928366 | ||||||
chr11:113928548
|
T | A | 1 | a0002c0002t0006g0204 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.214-2836T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928548 | ||||||
chr11:113928598
|
C | G | 5 | a0001c0005t0021g0068a0001c0005t0021g0383a0001c0005t0022g0384others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-2786C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928598 | ||||||
chr11:113928695
|
C | T | 62 | a0001c0001t0002g0182a0001c0001t0002g0297a0001c0001t0002g0299others(59): Show | 67 | HG00597.hp2 HG00639.hp2 HG01099.hp2 others(64): Show |
intron_variant | MODIFIER | c.214-2689C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928695 | ||||||
chr11:113928818
|
T | A | 1 | a0001c0001t0005g0047 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.214-2566T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928818 | ||||||
chr11:113928823
|
C | A | 1 | a0001c0001t0005g0047 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.214-2561C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113928823 | ||||||
chr11:113929045
|
T | C | 1 | a0001c0003t0003g0076 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.214-2339T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113929045 | ||||||
chr11:113929195
|
A | T | 1 | a0001c0001t0060g0195 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214-2189A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113929195 | ||||||
chr11:113929205
|
G | A | 1 | a0001c0001t0004g0291 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.214-2179G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113929205 | ||||||
chr11:113929485
|
T | C | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-1899T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113929485 | ||||||
chr11:113929564
|
T | C | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-1820T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113929564 | ||||||
chr11:113929576
|
A | T | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-1808A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113929576 | ||||||
chr11:113929756
|
G | A | 1 | a0001c0005t0021g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.214-1628G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113929756 | ||||||
chr11:113929778
|
G | T | 1 | a0001c0001t0005g0187 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214-1606G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113929778 | ||||||
chr11:113929922
|
C | T | 5 | a0001c0003t0003g0104a0004c0007t0019g0313a0004c0007t0019g0314others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-1462C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113929922 | ||||||
chr11:113930025
|
C | T | 1 | a0002c0002t0012g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.214-1359C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930025 | ||||||
chr11:113930026
|
G | A | 4 | a0003c0006t0023g0205a0003c0006t0023g0206a0003c0006t0023g0207others(1): Show | 4 | HG00323.hp2 HG01256.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-1358G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930026 | ||||||
chr11:113930075
|
G | A | 1 | a0001c0005t0021g0383 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.214-1309G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930075 | ||||||
chr11:113930182
|
G | T | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-1202G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930182 | ||||||
chr11:113930470
|
G | GT | 7 | a0001c0003t0003g0081a0002c0002t0034g0271a0004c0007t0019g0313others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-905dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113930470 | |||||
chr11:113930470
|
G | GTT | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-906_214-905dup others(2): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113930470 | |||||
chr11:113930487
|
C | CT | 22 | a0001c0001t0004g0300a0001c0001t0005g0056a0001c0001t0011g0283others(19): Show | 22 | HG01192.hp1 HG01243.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.214-878dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113930487 | |||||
chr11:113930487
|
CT | C | 15 | a0001c0001t0002g0311a0001c0001t0002g0320a0001c0001t0002g0349others(12): Show | 15 | HG01074.hp1 HG01074.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.214-878delT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113930487 | |||||
chr11:113930487
|
CTT | C | 11 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(8): Show | 12 | HG00738.hp1 HG01099.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-879_214-878del others(2): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113930487 | |||||
chr11:113930511
|
C | G | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-873C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930511 | ||||||
chr11:113930511
|
CAG | C | 36 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0032others(33): Show | 36 | HG00741.hp1 HG01081.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.214-870_214-869del others(2): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113930511 | |||||
chr11:113930513
|
G | C | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214-871G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930513 | ||||||
chr11:113930533
|
G | T | 1 | a0001c0001t0002g0352 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.214-851G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930533 | ||||||
chr11:113930692
|
G | A | 1 | a0002c0002t0001g0239 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.214-692G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930692 | ||||||
chr11:113930770
|
C | T | 3 | a0002c0002t0001g0168a0002c0002t0001g0263a0002c0002t0001g0266 | 3 | HG02572.hp1 HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.214-614C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930770 | ||||||
chr11:113930794
|
G | T | 60 | a0001c0001t0002g0182a0001c0001t0002g0297a0001c0001t0002g0299others(57): Show | 65 | HG00597.hp2 HG00639.hp2 HG01099.hp2 others(62): Show |
intron_variant | MODIFIER | c.214-590G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930794 | ||||||
chr11:113930833
|
T | A | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-551T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930833 | ||||||
chr11:113930869
|
A | G | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-515A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930869 | ||||||
chr11:113930881
|
A | T | 1 | a0002c0002t0001g0245 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.214-503A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930881 | ||||||
chr11:113930946
|
G | A | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-438G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113930946 | ||||||
chr11:113931165
|
C | T | 1 | a0001c0001t0042g0307 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.214-219C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113931165 | ||||||
chr11:113931230
|
A | T | 3 | a0001c0001t0005g0047a0001c0001t0005g0066a0001c0001t0005g0067 | 3 | HG02602.hp2 NA19001.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.214-154A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | chr11 | 113931230 | ||||||
chr11:113931249
|
G | GTCTAGGT others(2118): Show |
2 | a0003c0006t0023g0207a0003c0006t0046g0139 | 2 | HG00323.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.214-119_214-118ins others(2125): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113931249 | |||||
chr11:113931249
|
G | GTCTAGGT others(2119): Show |
1 | a0003c0006t0023g0206 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.214-119_214-118ins others(2126): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113931249 | |||||
chr11:113931249
|
G | GTCTAGGT others(2122): Show |
1 | a0003c0006t0023g0205 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214-119_214-118ins others(2129): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 113931249 | |||||
chr11:113931669
|
G | A | 2 | a0001c0001t0018g0048a0001c0001t0018g0051 | 2 | HG01081.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.259-89G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 3/8 | chr11 | 113931669 | ||||||
chr11:113931698
|
C | G | 2 | a0002c0002t0006g0166a0002c0002t0006g0270 | 2 | NA18747.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.259-60C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 3/8 | chr11 | 113931698 | ||||||
chr11:113931713
|
T | C | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-45T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 3/8 | chr11 | 113931713 | ||||||
chr11:113931878
|
C | T | 21 | a0002c0002t0008g0001a0002c0002t0008g0013a0002c0002t0008g0140others(18): Show | 24 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.368+11C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 4/8 | chr11 | 113931878 | ||||||
chr11:113931879
|
A | G | 318 | a0001c0001t0002g0182a0001c0001t0002g0297a0001c0001t0002g0299others(315): Show | 341 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(338): Show |
intron_variant | MODIFIER | c.368+12A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 4/8 | chr11 | 113931879 | ||||||
chr11:113931910
|
G | T | 1 | a0002c0002t0001g0237 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.368+43G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 4/8 | chr11 | 113931910 | ||||||
chr11:113932021
|
T | C | 7 | a0001c0001t0017g0116a0001c0001t0017g0117a0001c0001t0017g0119others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.368+154T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 4/8 | chr11 | 113932021 | ||||||
chr11:113932036
|
T | G | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.368+169T>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 4/8 | chr11 | 113932036 | ||||||
chr11:113932204
|
G | A | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.369-85G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 4/8 | chr11 | 113932204 | ||||||
chr11:113932212
|
C | T | 11 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(8): Show | 12 | HG00738.hp1 HG01099.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.369-77C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 4/8 | chr11 | 113932212 | ||||||
chr11:113932286
|
T | C | 11 | a0001c0001t0009g0022a0001c0001t0009g0197a0001c0001t0009g0198others(8): Show | 11 | HG00408.hp1 HG00544.hp2 HG02027.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.369-3T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 4/8 | chr11 | 113932286 | ||||||
chr11:113932639
|
T | C | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.538+181T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 5/8 | chr11 | 113932639 | ||||||
chr11:113932647
|
T | C | 8 | a0001c0003t0003g0004a0001c0003t0003g0080a0001c0003t0003g0084others(5): Show | 10 | HG00408.hp2 HG00621.hp1 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.538+189T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 5/8 | chr11 | 113932647 | ||||||
chr11:113932652
|
A | AAC | 318 | a0001c0001t0002g0182a0001c0001t0002g0297a0001c0001t0002g0299others(315): Show | 341 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(338): Show |
intron_variant | MODIFIER | c.538+196_538+197dup others(2): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 113932652 | |||||
chr11:113932749
|
G | A | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.539-187G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 5/8 | chr11 | 113932749 | ||||||
chr11:113933124
|
C | T | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.696+31C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113933124 | ||||||
chr11:113933133
|
C | A | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.696+40C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113933133 | ||||||
chr11:113933165
|
A | G | 92 | a0002c0002t0001g0005a0002c0002t0001g0014a0002c0002t0001g0016others(89): Show | 100 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.696+72A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113933165 | ||||||
chr11:113933182
|
T | A | 1 | a0001c0003t0003g0107 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.696+89T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113933182 | ||||||
chr11:113933254
|
C | G | 92 | a0002c0002t0001g0005a0002c0002t0001g0014a0002c0002t0001g0016others(89): Show | 100 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.696+161C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113933254 | ||||||
chr11:113933382
|
C | T | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.696+289C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113933382 | ||||||
chr11:113933386
|
T | C | 190 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(187): Show | 208 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.696+293T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113933386 | ||||||
chr11:113933484
|
A | ATT | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.696+400_696+401dup others(2): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 113933484 | |||||
chr11:113933604
|
C | T | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.696+511C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113933604 | ||||||
chr11:113933706
|
G | A | 3 | a0001c0001t0004g0373a0001c0001t0004g0378a0002c0002t0006g0166 | 3 | HG00597.hp2 HG02074.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.696+613G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113933706 | ||||||
chr11:113933720
|
G | A | 3 | a0002c0002t0001g0153a0002c0002t0001g0157a0002c0002t0001g0233 | 3 | NA18952.hp2 NA18967.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.696+627G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113933720 | ||||||
chr11:113933721
|
G | T | 1 | a0001c0003t0021g0073 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.696+628G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113933721 | ||||||
chr11:113933898
|
A | G | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.696+805A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113933898 | ||||||
chr11:113934389
|
A | G | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.696+1296A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113934389 | ||||||
chr11:113934390
|
G | GAAAGAAG others(13): Show |
4 | a0002c0002t0001g0368a0002c0002t0001g0369a0002c0002t0001g0371others(1): Show | 4 | HG02886.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.696+1304_696+1323d others(22): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 113934390 | |||||
chr11:113934407
|
AAAAAAAG others(55): Show |
A | 1 | a0001c0001t0002g0331 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.696+1336_696+1397d others(64): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 113934407 | |||||
chr11:113934548
|
G | A | 11 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(8): Show | 12 | HG00738.hp1 HG01099.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.696+1455G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113934548 | ||||||
chr11:113934609
|
A | T | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.696+1516A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113934609 | ||||||
chr11:113934630
|
G | A | 36 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0032others(33): Show | 36 | HG00741.hp1 HG01081.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.696+1537G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113934630 | ||||||
chr11:113934734
|
G | A | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.696+1641G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113934734 | ||||||
chr11:113934759
|
C | CT | 371 | a0001c0001t0002g0015a0001c0001t0002g0020a0001c0001t0002g0021others(368): Show | 399 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(396): Show |
intron_variant | MODIFIER | c.696+1679dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 113934759 | |||||
chr11:113934759
|
C | CTT | 14 | a0001c0001t0002g0186a0001c0001t0002g0191a0001c0001t0005g0062others(11): Show | 14 | HG00642.hp2 HG02129.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.696+1678_696+1679d others(4): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 113934759 | |||||
chr11:113934773
|
A | T | 1 | a0001c0001t0010g0324 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.696+1680A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113934773 | ||||||
chr11:113934791
|
T | C | 1 | a0001c0003t0049g0088 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.696+1698T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113934791 | ||||||
chr11:113934917
|
C | T | 1 | a0001c0005t0022g0384 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.696+1824C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113934917 | ||||||
chr11:113934928
|
T | C | 4 | a0003c0006t0023g0205a0003c0006t0023g0206a0003c0006t0023g0207others(1): Show | 4 | HG00323.hp2 HG01256.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.696+1835T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113934928 | ||||||
chr11:113934929
|
G | A | 4 | a0003c0006t0023g0205a0003c0006t0023g0206a0003c0006t0023g0207others(1): Show | 4 | HG00323.hp2 HG01256.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.696+1836G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113934929 | ||||||
chr11:113934953
|
A | G | 4 | a0003c0006t0023g0205a0003c0006t0023g0206a0003c0006t0023g0207others(1): Show | 4 | HG00323.hp2 HG01256.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.696+1860A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113934953 | ||||||
chr11:113935031
|
G | A | 1 | a0001c0001t0002g0341 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.696+1938G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935031 | ||||||
chr11:113935042
|
G | GCA | 11 | a0001c0001t0005g0187a0001c0001t0009g0199a0001c0001t0053g0069others(8): Show | 11 | HG00642.hp2 HG00735.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.696+1969_696+1970d others(4): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 113935042 | |||||
chr11:113935064
|
T | A | 23 | a0001c0001t0007g0131a0002c0002t0001g0005a0002c0002t0001g0014others(20): Show | 27 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.696+1971T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935064 | ||||||
chr11:113935112
|
T | G | 4 | a0004c0007t0019g0313a0004c0007t0019g0314a0004c0007t0019g0315others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+2019T>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935112 | ||||||
chr11:113935182
|
T | C | 1 | a0001c0001t0057g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.696+2089T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935182 | ||||||
chr11:113935242
|
T | C | 1 | a0001c0001t0004g0290 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.696+2149T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935242 | ||||||
chr11:113935281
|
C | G | 1 | a0001c0001t0005g0049 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.696+2188C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935281 | ||||||
chr11:113935290
|
G | C | 1 | a0001c0003t0021g0073 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.696+2197G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935290 | ||||||
chr11:113935413
|
G | A | 1 | a0001c0001t0064g0025 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.696+2320G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935413 | ||||||
chr11:113935454
|
A | ACTCAGGA others(273): Show |
3 | a0001c0001t0005g0039a0001c0001t0005g0187a0001c0001t0057g0167 | 3 | HG02145.hp1 HG02559.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.696+2362_696+2363i others(282): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 113935454 | |||||
chr11:113935454
|
A | ACTCAGGA others(271): Show |
35 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0032others(32): Show | 35 | HG00741.hp1 HG01081.hp1 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.696+2362_696+2363i others(280): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 113935454 | |||||
chr11:113935458
|
A | C | 38 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0032others(35): Show | 38 | HG00741.hp1 HG01081.hp1 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.696+2365A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935458 | ||||||
chr11:113935459
|
TC | T | 38 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0032others(35): Show | 38 | HG00741.hp1 HG01081.hp1 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.696+2367delC | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935459 | ||||||
chr11:113935535
|
C | T | 46 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(43): Show | 52 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.696+2442C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935535 | ||||||
chr11:113935632
|
C | A | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.696+2539C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935632 | ||||||
chr11:113935633
|
C | G | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.696+2540C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935633 | ||||||
chr11:113935634
|
C | A | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.696+2541C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935634 | ||||||
chr11:113935635
|
A | T | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.696+2542A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935635 | ||||||
chr11:113935637
|
T | G | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.696+2544T>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935637 | ||||||
chr11:113935639
|
T | G | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.696+2546T>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935639 | ||||||
chr11:113935640
|
G | T | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.696+2547G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935640 | ||||||
chr11:113935641
|
A | G | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.696+2548A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935641 | ||||||
chr11:113935642
|
A | T | 1 | a0006c0012t0065g0030 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.696+2549A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935642 | ||||||
chr11:113935656
|
G | C | 1 | a0001c0003t0003g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.696+2563G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935656 | ||||||
chr11:113935743
|
C | G | 5 | a0001c0005t0021g0068a0001c0005t0021g0383a0001c0005t0022g0384others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+2650C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935743 | ||||||
chr11:113935778
|
C | T | 7 | a0001c0001t0017g0116a0001c0001t0017g0117a0001c0001t0017g0119others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.696+2685C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935778 | ||||||
chr11:113935814
|
G | A | 6 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(3): Show | 6 | HG01884.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.696+2721G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935814 | ||||||
chr11:113935921
|
G | A | 2 | a0002c0002t0012g0133a0002c0002t0045g0147 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.696+2828G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113935921 | ||||||
chr11:113935975
|
CAA | C | 4 | a0004c0007t0019g0313a0004c0007t0019g0314a0004c0007t0019g0315others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.696+2884_696+2885d others(4): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 113935975 | |||||
chr11:113936022
|
A | G | 10 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.696+2929A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936022 | ||||||
chr11:113936260
|
C | T | 1 | a0002c0002t0034g0271 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.696+3167C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936260 | ||||||
chr11:113936302
|
G | A | 1 | a0001c0001t0002g0341 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.696+3209G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936302 | ||||||
chr11:113936459
|
G | A | 119 | a0001c0001t0002g0182a0001c0001t0002g0297a0001c0001t0002g0299others(116): Show | 124 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.696+3366G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936459 | ||||||
chr11:113936563
|
A | G | 1 | a0003c0006t0023g0205 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.696+3470A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936563 | ||||||
chr11:113936593
|
C | T | 21 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(18): Show | 22 | HG00323.hp2 HG00738.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.696+3500C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936593 | ||||||
chr11:113936613
|
G | A | 1 | a0001c0001t0007g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.696+3520G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936613 | ||||||
chr11:113936620
|
G | A | 1 | a0001c0003t0021g0073 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.696+3527G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936620 | ||||||
chr11:113936674
|
T | A | 21 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(18): Show | 22 | HG00323.hp2 HG00738.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.696+3581T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936674 | ||||||
chr11:113936868
|
T | C | 6 | a0001c0001t0017g0116a0001c0001t0017g0117a0001c0001t0017g0119others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.696+3775T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936868 | ||||||
chr11:113936885
|
G | A | 272 | a0001c0001t0002g0182a0001c0001t0002g0297a0001c0001t0002g0299others(269): Show | 291 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.696+3792G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936885 | ||||||
chr11:113936895
|
A | G | 1 | a0001c0001t0011g0113 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.696+3802A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936895 | ||||||
chr11:113936905
|
A | G | 7 | a0001c0001t0002g0319a0001c0001t0002g0328a0001c0001t0002g0330others(4): Show | 7 | HG00438.hp2 HG02080.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.696+3812A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936905 | ||||||
chr11:113936927
|
A | T | 1 | a0005c0009t0017g0318 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.696+3834A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936927 | ||||||
chr11:113936985
|
T | G | 1 | a0002c0002t0001g0241 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.696+3892T>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113936985 | ||||||
chr11:113937095
|
G | C | 21 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(18): Show | 22 | HG00323.hp2 HG00738.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.696+4002G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113937095 | ||||||
chr11:113937169
|
G | A | 1 | a0002c0002t0063g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.696+4076G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113937169 | ||||||
chr11:113937208
|
C | T | 5 | a0001c0005t0021g0068a0001c0005t0021g0383a0001c0005t0022g0384others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+4115C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113937208 | ||||||
chr11:113937252
|
G | A | 1 | a0001c0001t0002g0342 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.696+4159G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113937252 | ||||||
chr11:113937259
|
G | A | 1 | a0002c0002t0001g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.696+4166G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113937259 | ||||||
chr11:113937342
|
C | G | 1 | a0001c0001t0057g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.696+4249C>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113937342 | ||||||
chr11:113937373
|
T | C | 21 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(18): Show | 22 | HG00323.hp2 HG00738.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.696+4280T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113937373 | ||||||
chr11:113937460
|
C | T | 7 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(4): Show | 7 | HG00738.hp1 HG01099.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.696+4367C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113937460 | ||||||
chr11:113937803
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.696+4710G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113937803 | ||||||
chr11:113937805
|
G | A | 47 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(44): Show | 53 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.696+4712G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113937805 | ||||||
chr11:113938026
|
G | A | 24 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0032others(21): Show | 24 | HG01928.hp1 HG02083.hp2 HG02602.hp2 others(21): Show |
intron_variant | MODIFIER | c.696+4933G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113938026 | ||||||
chr11:113938035
|
G | A | 273 | a0001c0001t0002g0182a0001c0001t0002g0297a0001c0001t0002g0299others(270): Show | 292 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.696+4942G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113938035 | ||||||
chr11:113938083
|
T | A | 21 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(18): Show | 22 | HG00323.hp2 HG00738.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.697-4899T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113938083 | ||||||
chr11:113938126
|
A | T | 2 | a0002c0002t0008g0013a0002c0002t0008g0214 | 3 | HG01069.hp1 HG01071.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.697-4856A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113938126 | ||||||
chr11:113938135
|
T | C | 1 | a0001c0001t0007g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.697-4847T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113938135 | ||||||
chr11:113938365
|
T | A | 1 | a0001c0001t0002g0353 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.697-4617T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113938365 | ||||||
chr11:113938678
|
A | G | 14 | a0001c0003t0003g0007a0001c0003t0003g0078a0001c0003t0003g0079others(11): Show | 15 | HG00673.hp2 HG01192.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.697-4304A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113938678 | ||||||
chr11:113938756
|
G | A | 1 | a0005c0009t0017g0318 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.697-4226G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113938756 | ||||||
chr11:113938774
|
C | T | 1 | a0001c0001t0005g0032 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.697-4208C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113938774 | ||||||
chr11:113938856
|
G | A | 4 | a0002c0002t0001g0368a0002c0002t0001g0369a0002c0002t0001g0371others(1): Show | 4 | HG02886.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.697-4126G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113938856 | ||||||
chr11:113938926
|
C | T | 21 | a0002c0002t0008g0001a0002c0002t0008g0013a0002c0002t0008g0140others(18): Show | 24 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.697-4056C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113938926 | ||||||
chr11:113938944
|
G | A | 46 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(43): Show | 52 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.697-4038G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113938944 | ||||||
chr11:113939170
|
C | T | 17 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(14): Show | 18 | HG00738.hp1 HG01099.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.697-3812C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113939170 | ||||||
chr11:113939260
|
C | T | 17 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(14): Show | 18 | HG00738.hp1 HG01099.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.697-3722C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113939260 | ||||||
chr11:113939306
|
G | A | 1 | a0001c0001t0051g0332 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.697-3676G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113939306 | ||||||
chr11:113939326
|
T | C | 46 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(43): Show | 52 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.697-3656T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113939326 | ||||||
chr11:113939389
|
T | C | 1 | a0002c0002t0006g0174 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.697-3593T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113939389 | ||||||
chr11:113939406
|
C | A | 21 | a0002c0002t0008g0001a0002c0002t0008g0013a0002c0002t0008g0140others(18): Show | 24 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.697-3576C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113939406 | ||||||
chr11:113939436
|
C | A | 1 | a0001c0003t0003g0109 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.697-3546C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113939436 | ||||||
chr11:113939601
|
C | T | 1 | a0002c0002t0008g0210 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.697-3381C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113939601 | ||||||
chr11:113939888
|
G | GT | 90 | a0001c0001t0002g0182a0001c0001t0002g0191a0001c0001t0002g0297others(87): Show | 95 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.697-3078dupT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 113939888 | |||||
chr11:113939888
|
G | GTT | 7 | a0001c0001t0002g0323a0001c0001t0004g0308a0001c0001t0007g0132others(4): Show | 7 | HG01081.hp2 HG01361.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.697-3079_697-3078d others(4): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 113939888 | |||||
chr11:113939888
|
GTT | G | 6 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(3): Show | 6 | HG01884.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.697-3079_697-3078d others(4): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 113939888 | |||||
chr11:113940012
|
G | A | 11 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(8): Show | 12 | HG00738.hp1 HG01099.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.697-2970G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113940012 | ||||||
chr11:113940089
|
T | A | 17 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(14): Show | 18 | HG00738.hp1 HG01099.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.697-2893T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113940089 | ||||||
chr11:113940218
|
T | C | 5 | a0001c0001t0005g0046a0001c0001t0005g0064a0001c0001t0018g0048others(2): Show | 5 | HG01081.hp1 HG01261.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.697-2764T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113940218 | ||||||
chr11:113940248
|
C | T | 8 | a0002c0002t0008g0001a0002c0002t0008g0013a0002c0002t0008g0140others(5): Show | 11 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.697-2734C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113940248 | ||||||
chr11:113940349
|
G | A | 1 | a0001c0003t0003g0099 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.697-2633G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113940349 | ||||||
chr11:113940355
|
A | G | 6 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(3): Show | 6 | HG01884.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.697-2627A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113940355 | ||||||
chr11:113940507
|
A | C | 5 | a0001c0001t0042g0307a0003c0006t0023g0205a0003c0006t0023g0206others(2): Show | 5 | HG00323.hp2 HG01256.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.697-2475A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113940507 | ||||||
chr11:113940703
|
C | T | 1 | a0001c0001t0010g0324 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.697-2279C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113940703 | ||||||
chr11:113940838
|
T | C | 1 | a0001c0001t0064g0025 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.697-2144T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113940838 | ||||||
chr11:113940848
|
C | T | 1 | a0001c0003t0003g0089 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.697-2134C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113940848 | ||||||
chr11:113940963
|
G | A | 1 | a0001c0001t0009g0363 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.697-2019G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113940963 | ||||||
chr11:113940972
|
G | A | 10 | a0002c0002t0020g0144a0002c0002t0020g0145a0002c0002t0020g0203others(7): Show | 11 | HG01884.hp2 HG02109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.697-2010G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113940972 | ||||||
chr11:113941047
|
A | G | 4 | a0002c0002t0020g0144a0002c0002t0020g0145a0002c0002t0020g0203others(1): Show | 5 | HG02109.hp2 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.697-1935A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113941047 | ||||||
chr11:113941080
|
G | A | 2 | a0001c0001t0005g0187a0001c0001t0057g0167 | 2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.697-1902G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113941080 | ||||||
chr11:113941119
|
G | A | 36 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0032others(33): Show | 36 | HG00741.hp1 HG01081.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.697-1863G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113941119 | ||||||
chr11:113941125
|
C | T | 52 | a0001c0003t0003g0004a0001c0003t0003g0007a0001c0003t0003g0008others(49): Show | 58 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.697-1857C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113941125 | ||||||
chr11:113941316
|
A | G | 5 | a0001c0005t0021g0068a0001c0005t0021g0383a0001c0005t0022g0384others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.697-1666A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113941316 | ||||||
chr11:113941418
|
A | C | 8 | a0002c0002t0012g0133a0002c0002t0012g0148a0002c0002t0012g0216others(5): Show | 8 | HG01109.hp2 HG02145.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.697-1564A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113941418 | ||||||
chr11:113941558
|
C | A | 1 | a0001c0005t0021g0383 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.697-1424C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113941558 | ||||||
chr11:113941785
|
GTCCTATC others(8): Show |
G | 1 | a0007c0011t0001g0235 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.697-1194_697-1180d others(17): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 113941785 | |||||
chr11:113941899
|
G | A | 1 | a0002c0002t0006g0172 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.697-1083G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113941899 | ||||||
chr11:113941909
|
G | A | 2 | a0001c0003t0003g0009a0001c0003t0003g0076 | 3 | NA18942.hp2 NA18998.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.697-1073G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113941909 | ||||||
chr11:113942011
|
G | A | 306 | a0001c0001t0002g0182a0001c0001t0002g0186a0001c0001t0002g0297others(303): Show | 329 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(326): Show |
intron_variant | MODIFIER | c.697-971G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942011 | ||||||
chr11:113942027
|
A | G | 1 | a0001c0001t0002g0337 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.697-955A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942027 | ||||||
chr11:113942097
|
C | T | 91 | a0002c0002t0001g0005a0002c0002t0001g0014a0002c0002t0001g0016others(88): Show | 99 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.697-885C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942097 | ||||||
chr11:113942167
|
G | C | 21 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(18): Show | 22 | HG00323.hp2 HG00738.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.697-815G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942167 | ||||||
chr11:113942173
|
C | A | 91 | a0002c0002t0001g0005a0002c0002t0001g0014a0002c0002t0001g0016others(88): Show | 99 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.697-809C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942173 | ||||||
chr11:113942219
|
T | G | 1 | a0001c0005t0021g0383 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.697-763T>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942219 | ||||||
chr11:113942224
|
C | T | 1 | a0002c0002t0044g0149 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.697-758C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942224 | ||||||
chr11:113942444
|
A | T | 1 | a0007c0011t0001g0235 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.697-538A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942444 | ||||||
chr11:113942446
|
C | T | 1 | a0001c0003t0021g0073 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.697-536C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942446 | ||||||
chr11:113942464
|
A | G | 3 | a0001c0001t0002g0185a0001c0001t0002g0365a0001c0001t0002g0366 | 3 | HG00639.hp1 HG01074.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.697-518A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942464 | ||||||
chr11:113942546
|
A | G | 1 | a0001c0001t0040g0120 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.697-436A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942546 | ||||||
chr11:113942601
|
T | C | 4 | a0002c0002t0001g0368a0002c0002t0001g0369a0002c0002t0001g0371others(1): Show | 4 | HG02886.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.697-381T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942601 | ||||||
chr11:113942710
|
G | C | 1 | a0002c0002t0001g0238 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.697-272G>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942710 | ||||||
chr11:113942845
|
C | T | 7 | a0001c0001t0004g0006a0001c0001t0004g0304a0001c0001t0007g0006others(4): Show | 8 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.697-137C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942845 | ||||||
chr11:113942891
|
T | A | 21 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(18): Show | 22 | HG00323.hp2 HG00738.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.697-91T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942891 | ||||||
chr11:113942931
|
G | T | 1 | a0001c0001t0002g0344 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.697-51G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 6/8 | chr11 | 113942931 | ||||||
chr11:113943213
|
T | C | 2 | a0001c0001t0002g0279a0001c0001t0002g0280 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.907+21T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113943213 | ||||||
chr11:113943310
|
G | A | 7 | a0002c0002t0001g0180a0002c0002t0001g0261a0002c0002t0001g0265others(4): Show | 7 | HG00738.hp2 HG02004.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.907+118G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113943310 | ||||||
chr11:113943428
|
G | T | 2 | a0001c0001t0002g0320a0001c0001t0002g0321 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.907+236G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113943428 | ||||||
chr11:113943534
|
G | A | 1 | a0001c0001t0002g0329 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.907+342G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113943534 | ||||||
chr11:113943545
|
G | A | 1 | a0002c0002t0015g0249 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.907+353G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113943545 | ||||||
chr11:113943574
|
G | A | 317 | a0001c0001t0002g0186a0001c0001t0002g0299a0001c0001t0004g0003others(314): Show | 340 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(337): Show |
intron_variant | MODIFIER | c.907+382G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113943574 | ||||||
chr11:113943666
|
C | A | 1 | a0001c0001t0002g0333 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.907+474C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113943666 | ||||||
chr11:113943702
|
A | T | 1 | a0001c0001t0007g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.907+510A>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113943702 | ||||||
chr11:113943768
|
C | T | 1 | a0002c0002t0001g0240 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.907+576C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113943768 | ||||||
chr11:113943903
|
G | A | 292 | a0001c0001t0002g0299a0001c0001t0004g0003a0001c0001t0004g0006others(289): Show | 312 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.908-670G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113943903 | ||||||
chr11:113943985
|
G | T | 1 | a0001c0003t0003g0109 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.908-588G>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113943985 | ||||||
chr11:113944022
|
CT | C | 201 | a0001c0001t0002g0299a0001c0001t0002g0320a0001c0001t0004g0003others(198): Show | 215 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.908-535delT | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 113944022 | |||||
chr11:113944025
|
T | C | 13 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(10): Show | 13 | HG00738.hp1 HG01099.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.908-548T>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113944025 | ||||||
chr11:113944101
|
C | T | 1 | a0001c0001t0010g0339 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.908-472C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113944101 | ||||||
chr11:113944208
|
C | T | 6 | a0003c0004t0025g0070a0003c0004t0025g0151a0003c0004t0025g0152others(3): Show | 6 | HG01884.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.908-365C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113944208 | ||||||
chr11:113944264
|
C | T | 1 | a0002c0002t0059g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.908-309C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113944264 | ||||||
chr11:113944265
|
G | A | 1 | a0001c0005t0021g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.908-308G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113944265 | ||||||
chr11:113944305
|
A | C | 1 | a0007c0011t0001g0235 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.908-268A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113944305 | ||||||
chr11:113944316
|
C | T | 1 | a0001c0001t0004g0372 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.908-257C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113944316 | ||||||
chr11:113944392
|
T | A | 1 | a0002c0002t0024g0259 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.908-181T>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 7/8 | chr11 | 113944392 | ||||||
chr11:113944784
|
C | T | 1 | a0001c0001t0009g0364 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1090+29C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113944784 | ||||||
chr11:113944785
|
G | A | 13 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(10): Show | 13 | HG00738.hp1 HG01099.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1090+30G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113944785 | ||||||
chr11:113944816
|
C | T | 13 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(10): Show | 13 | HG00738.hp1 HG01099.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1090+61C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113944816 | ||||||
chr11:113944839
|
C | T | 8 | a0001c0001t0011g0026a0001c0001t0011g0113a0001c0001t0011g0178others(5): Show | 8 | HG02280.hp2 HG02559.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1090+84C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113944839 | ||||||
chr11:113945161
|
A | G | 13 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(10): Show | 13 | HG00738.hp1 HG01099.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1090+406A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113945161 | ||||||
chr11:113945214
|
A | G | 3 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0226 | 3 | HG02886.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1090+459A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113945214 | ||||||
chr11:113945398
|
G | A | 1 | a0005c0009t0017g0318 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1091-504G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113945398 | ||||||
chr11:113945463
|
A | C | 1 | a0001c0005t0021g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1091-439A>C | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113945463 | ||||||
chr11:113945655
|
C | A | 21 | a0002c0002t0008g0001a0002c0002t0008g0013a0002c0002t0008g0140others(18): Show | 24 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1091-247C>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113945655 | ||||||
chr11:113945662
|
G | A | 1 | a0002c0002t0033g0163 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1091-240G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113945662 | ||||||
chr11:113945675
|
A | G | 1 | a0001c0001t0002g0341 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1091-227A>G | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113945675 | ||||||
chr11:113945718
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0350 | 3 | HG03491.hp2 HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1091-184G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113945718 | ||||||
chr11:113945784
|
C | T | 13 | a0002c0002t0014g0150a0002c0002t0014g0221a0002c0002t0014g0224others(10): Show | 13 | HG00738.hp1 HG01099.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1091-118C>T | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113945784 | ||||||
chr11:113945824
|
G | A | 1 | a0001c0005t0021g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1091-78G>A | HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 8/8 | chr11 | 113945824 |