geneid | 3081 |
---|---|
ensemblid | ENSG00000113924.12 |
hgncid | 4892 |
symbol | HGD |
name | homogentisate 1,2-dioxygenase |
refseq_nuc | NM_000187.4 |
refseq_prot | NP_000178.2 |
ensembl_nuc | ENST00000283871.10 |
ensembl_prot | ENSP00000283871.5 |
mane_status | MANE Select |
chr | chr3 |
start | 120628172 |
end | 120682239 |
strand | - |
ver | v1.2 |
region | chr3:120628172-120682239 |
region5000 | chr3:120623172-120687239 |
regionname0 | HGD_chr3_120628172_120682239 |
regionname5000 | HGD_chr3_120623172_120687239 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 445 | 249 | 67 | 61 | 83 | 12 | 25 | 65 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0002 | 1/0 | 445 | 115 | 15 | 12 | 64 | 4 | 19 | 48 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0003 | 0/0 | 445 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0004 | 0/0 | 445 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0005 | 0/0 | 445 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0006 | 0/0 | 445 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0007 | 0/0 | 445 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1338 | 236 | 63 | 58 | 82 | 9 | 23 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
c0002 | 1/0 | 1338 | 112 | 13 | 12 | 63 | 4 | 19 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
c0003 | 0/0 | 1338 | 5 | 4 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
c0004 | 0/0 | 1338 | 5 | 0 | 1 | 1 | 2 | 1 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
c0005 | 0/0 | 1338 | 5 | 4 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
c0006 | 0/0 | 1338 | 3 | 0 | 2 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
c0007 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
c0008 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
c0009 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
c0010 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
c0011 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
c0012 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
g0348 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1338 | 236 | 63 | 58 | 82 | 9 | 23 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0001c0003 | 0/0 | 1338 | 5 | 4 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0001c0004 | 0/0 | 1338 | 5 | 0 | 1 | 1 | 2 | 1 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0001c0006 | 0/0 | 1338 | 3 | 0 | 2 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0002c0002 | 1/0 | 1338 | 112 | 13 | 12 | 63 | 4 | 19 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0002c0007 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0002c0010 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0003c0005 | 0/0 | 1338 | 5 | 4 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0004c0008 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0005c0012 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0006c0011 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0007c0009 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1674 | 235 | 63 | 57 | 82 | 9 | 23 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0001c0001t0002 | 0/0 | 1674 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0001c0003t0001 | 0/0 | 1674 | 5 | 4 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0001c0004t0001 | 0/0 | 1674 | 5 | 0 | 1 | 1 | 2 | 1 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0001c0006t0001 | 0/0 | 1674 | 3 | 0 | 2 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0002c0002t0001 | 1/0 | 1674 | 112 | 13 | 12 | 63 | 4 | 19 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0002c0007t0001 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0002c0010t0001 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0003c0005t0001 | 0/0 | 1674 | 5 | 4 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0004c0008t0001 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0005c0012t0001 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0006c0011t0001 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
a0007c0009t0001 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | copy fasta | chr3 | 120623172 | 120687239 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0001g0348 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0006t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0001c0006t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0007t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0007t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0002c0010t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0003c0005t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0003c0005t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0003c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0003c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0003c0005t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0004c0008t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0004c0008t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0005c0012t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0006c0011t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
a0007c0009t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0305 | EUR | GBR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0291 | EUR | FIN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0338 | EUR | FIN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | FIN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0332 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0312 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0298 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01099 | hp1 | a0003 | c0005 | t0001 | g0032 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01106 | hp1 | a0001 | c0004 | t0001 | g0068 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0329 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01192 | hp2 | a0001 | c0006 | t0001 | g0015 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0304 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01496 | hp1 | a0001 | c0006 | t0001 | g0015 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0019 | EUR | IBS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01516 | hp2 | a0001 | c0004 | t0001 | g0067 | EUR | IBS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0019 | EUR | IBS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01884 | hp1 | a0006 | c0011 | t0001 | g0041 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0296 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0299 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0293 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0297 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02132 | hp2 | a0001 | c0004 | t0001 | g0076 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | CDX | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0308 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0301 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0258 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0267 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02622 | hp2 | a0004 | c0008 | t0001 | g0049 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0290 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0283 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0179 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0306 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02809 | hp1 | a0003 | c0005 | t0001 | g0028 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0260 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0261 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0177 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0320 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0294 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0070 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03209 | hp2 | a0005 | c0012 | t0001 | g0050 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0292 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0295 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03453 | hp1 | a0004 | c0008 | t0001 | g0054 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03453 | hp2 | a0001 | c0003 | t0001 | g0058 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0269 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0257 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0327 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03579 | hp1 | a0002 | c0007 | t0001 | g0256 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0303 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0343 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03669 | hp1 | a0001 | c0004 | t0001 | g0243 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03704 | hp1 | a0001 | c0006 | t0001 | g0221 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0069 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0018 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0339 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0302 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0272 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0326 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0317 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0307 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0340 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0088 | AFR | YRI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0328 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0347 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0333 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18983 | hp2 | a0007 | c0009 | t0001 | g0314 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18990 | hp1 | a0002 | c0010 | t0001 | g0315 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0345 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ASW | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA20805 | hp1 | a0001 | c0004 | t0001 | g0111 | EUR | TSI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0122 | EUR | TSI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0259 | SAS | GIH | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | GIH | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02109 | hp1 | a0003 | c0005 | t0001 | g0029 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02109 | hp2 | a0003 | c0005 | t0001 | g0031 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0289 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02559 | hp1 | a0002 | c0007 | t0001 | g0321 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | USA | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0300 | AFR | USA | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0253 | AFR | USA | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA20300 | hp2 | a0003 | c0005 | t0001 | g0030 | AFR | USA | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0348 | REF | REF | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0288 | REF | REF | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:120633207
|
G | C | 1 | a0006 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1128C>G | p.Asp376Glu | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/14 | 1256/1674 | 1128/1338 | 376/445 | chr3 | 120633207 | ||
chr3:120638538
|
G | C | 1 | a0007 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.923C>G | p.Pro308Arg | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/14 | 1051/1674 | 923/1338 | 308/445 | chr3 | 120638538 | ||
chr3:120638542
|
G | A | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.919C>T | p.Arg307Cys | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/14 | 1047/1674 | 919/1338 | 307/445 | chr3 | 120638542 | ||
chr3:120638566
|
T | C | 1 | a0004 | 2 | HG02622.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.895A>G | p.Thr299Ala | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/14 | 1023/1674 | 895/1338 | 299/445 | chr3 | 120638566 | ||
chr3:120670469
|
T | A | 5 | a0001a0003a0004others(2): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
missense_variant | MODERATE | c.240A>T | p.Gln80His | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/14 | 368/1674 | 240/1338 | 80/445 | chr3 | 120670469 | ||
chr3:120674935
|
C | A | 1 | a0003 | 5 | HG01099.hp1 HG02109.hp1 HG02109.hp2 others(2): Show |
missense_variant | MODERATE | c.142G>T | p.Ala48Ser | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/14 | 270/1674 | 142/1338 | 48/445 | chr3 | 120674935 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:120628497
|
C | T | 2 | a0001c0003a0002c0007 | 7 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(4): Show |
synonymous_variant | LOW | c.1221G>A | p.Ala407Ala | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 14/14 | 1349/1674 | 1221/1338 | 407/445 | chr3 | 120628497 | ||
chr3:120628527
|
T | G | 1 | a0001c0004 | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.1191A>C | p.Ala397Ala | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 14/14 | 1319/1674 | 1191/1338 | 397/445 | chr3 | 120628527 | ||
chr3:120633156
|
A | G | 1 | a0001c0006 | 3 | HG01192.hp2 HG01496.hp1 HG03704.hp1 |
synonymous_variant | LOW | c.1179T>C | p.Asp393Asp | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/14 | 1307/1674 | 1179/1338 | 393/445 | chr3 | 120633156 | ||
chr3:120647048
|
C | A | 1 | a0002c0010 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.474G>T | p.Pro158Pro | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 8/14 | 602/1674 | 474/1338 | 158/445 | chr3 | 120647048 | ||
chr3:120650836
|
G | A | 1 | a0001c0004 | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
synonymous_variant | LOW | c.372C>T | p.Asp124Asp | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/14 | 500/1674 | 372/1338 | 124/445 | chr3 | 120650836 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:120682219
|
A | G | 1 | a0001c0001t0002 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-108T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/14 | 108 | chr3 | 120682219 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:120629343
|
C | T | 6 | a0001c0003t0001g0058a0001c0003t0001g0070a0001c0003t0001g0088others(3): Show | 6 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1189-814G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120629343 | ||||||
chr3:120629444
|
A | G | 1 | a0005c0012t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1189-915T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120629444 | ||||||
chr3:120629618
|
G | A | 1 | a0005c0012t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1189-1089C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120629618 | ||||||
chr3:120629868
|
G | A | 1 | a0006c0011t0001g0041 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1189-1339C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120629868 | ||||||
chr3:120629920
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1189-1391T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120629920 | ||||||
chr3:120630033
|
A | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1189-1504T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630033 | ||||||
chr3:120630470
|
G | A | 6 | a0001c0003t0001g0058a0001c0003t0001g0070a0001c0003t0001g0088others(3): Show | 6 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1189-1941C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630470 | ||||||
chr3:120630556
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1189-2027T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630556 | ||||||
chr3:120630594
|
C | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(63): Show | 68 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1189-2065G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630594 | ||||||
chr3:120630684
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1189-2155G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630684 | ||||||
chr3:120630708
|
A | G | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1189-2179T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630708 | ||||||
chr3:120630798
|
T | TATATATA others(4): Show |
1 | a0002c0002t0001g0325 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1189-2270_1189-226 others(15): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TATATATA others(14): Show |
1 | a0001c0001t0001g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1189-2270_1189-226 others(25): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTA | 12 | a0001c0001t0001g0057a0001c0001t0001g0105a0001c0001t0001g0113others(9): Show | 13 | HG01099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1189-2271_1189-227 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTATA | 13 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0056others(10): Show | 13 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1189-2273_1189-227 others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTATATA | 16 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0062others(13): Show | 16 | HG00738.hp2 HG01109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1189-2275_1189-227 others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTATATAT others(1): Show |
3 | a0001c0001t0001g0053a0001c0001t0001g0099a0001c0003t0001g0070 | 3 | HG00741.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1189-2277_1189-227 others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTATATAT others(3): Show |
2 | a0001c0001t0001g0034a0002c0002t0001g0274 | 2 | HG01891.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1189-2279_1189-227 others(14): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTATATAT others(5): Show |
8 | a0001c0001t0001g0043a0001c0001t0001g0083a0001c0003t0001g0088others(5): Show | 8 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1189-2281_1189-227 others(16): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTATATAT others(7): Show |
3 | a0001c0001t0001g0005a0001c0001t0001g0135a0001c0001t0001g0231 | 4 | HG02572.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1189-2283_1189-227 others(18): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0036a0001c0001t0001g0234 | 2 | NA18993.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1189-2285_1189-227 others(20): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTATATAT others(11): Show |
9 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0052others(6): Show | 12 | HG02451.hp2 HG02486.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1189-2287_1189-227 others(22): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTATATAT others(13): Show |
6 | a0001c0001t0001g0047a0001c0001t0001g0082a0002c0002t0001g0182others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-2289_1189-227 others(24): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTATATAT others(15): Show |
4 | a0001c0001t0001g0059a0001c0001t0001g0162a0002c0002t0001g0260others(1): Show | 4 | HG00639.hp1 HG01175.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1189-2291_1189-227 others(26): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTATATAT others(17): Show |
1 | a0004c0008t0001g0054 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1189-2293_1189-227 others(28): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTATATAT others(19): Show |
1 | a0001c0001t0001g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1189-2295_1189-227 others(30): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
T | TTATATAT others(21): Show |
1 | a0001c0001t0001g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1189-2297_1189-227 others(32): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
TTA | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(94): Show | 107 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.1189-2271_1189-227 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
TTATATA | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0104others(28): Show | 35 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1189-2275_1189-227 others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
TTATATAT others(1): Show |
T | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0152 | 3 | HG02055.hp2 NA18944.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1189-2277_1189-227 others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630798
|
TTATATAT others(3): Show |
T | 2 | a0001c0001t0001g0045a0001c0001t0001g0073 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1189-2279_1189-227 others(14): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | ||||||
chr3:120630823
|
T | TACAC | 3 | a0001c0001t0001g0197a0002c0002t0001g0263a0002c0002t0001g0285 | 3 | HG00621.hp2 HG02071.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1189-2295_1189-229 others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630823 | ||||||
chr3:120630825
|
T | TATACAC | 14 | a0001c0001t0001g0063a0001c0001t0001g0108a0001c0001t0001g0144others(11): Show | 15 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.1189-2297_1189-229 others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | ||||||
chr3:120630825
|
T | TATATACA others(1): Show |
4 | a0001c0001t0001g0064a0001c0001t0001g0190a0002c0002t0001g0294others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-2297_1189-229 others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | ||||||
chr3:120630825
|
T | TATATATA others(1): Show |
13 | a0001c0001t0001g0007a0001c0001t0001g0102a0001c0001t0001g0103others(10): Show | 14 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-2297_1189-229 others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | ||||||
chr3:120630825
|
T | TATATATA others(3): Show |
1 | a0001c0001t0001g0060 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1189-2297_1189-229 others(14): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | ||||||
chr3:120630825
|
T | TATATATA others(3): Show |
4 | a0001c0001t0001g0100a0001c0001t0001g0156a0002c0002t0001g0249others(1): Show | 4 | HG00639.hp2 HG02083.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-2297_1189-229 others(14): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | ||||||
chr3:120630825
|
T | TATATATA others(5): Show |
2 | a0001c0001t0001g0208a0002c0002t0001g0320 | 2 | HG02970.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1189-2297_1189-229 others(16): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | ||||||
chr3:120630825
|
T | TATATATA others(9): Show |
2 | a0002c0002t0001g0259a0002c0002t0001g0299 | 2 | HG01975.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1189-2297_1189-229 others(20): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | ||||||
chr3:120630825
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0336 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1189-2297_1189-229 others(30): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | ||||||
chr3:120630825
|
T | TATATATA others(23): Show |
1 | a0001c0001t0001g0101 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1189-2297_1189-229 others(34): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | ||||||
chr3:120630827
|
C | T | 82 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(79): Show | 86 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1189-2298G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630827 | ||||||
chr3:120630829
|
C | T | 64 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(61): Show | 67 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1189-2300G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630829 | ||||||
chr3:120630831
|
T | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0071others(28): Show | 32 | HG00280.hp1 HG00621.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1189-2302A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | ||||||
chr3:120630831
|
T | TATAC | 6 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0184others(3): Show | 7 | HG01516.hp1 HG01517.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-2303_1189-230 others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | ||||||
chr3:120630831
|
T | TATATAC | 3 | a0001c0001t0001g0344a0002c0002t0001g0267a0003c0005t0001g0030 | 3 | HG02602.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1189-2303_1189-230 others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | ||||||
chr3:120630831
|
T | TATATATA others(1): Show |
3 | a0002c0002t0001g0289a0002c0002t0001g0290a0002c0002t0001g0304 | 3 | HG01433.hp1 HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1189-2303_1189-230 others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | ||||||
chr3:120630831
|
T | TATATATA others(5): Show |
5 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0081others(2): Show | 6 | HG02258.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-2303_1189-230 others(16): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | ||||||
chr3:120630831
|
T | TATATATA others(7): Show |
2 | a0001c0001t0001g0089a0002c0002t0001g0253 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1189-2303_1189-230 others(18): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | ||||||
chr3:120630831
|
T | TATATATA others(9): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0133 | 4 | HG00099.hp2 HG01515.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-2303_1189-230 others(20): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | ||||||
chr3:120630833
|
C | T | 5 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0116others(2): Show | 5 | HG02896.hp1 HG03098.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-2304G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630833 | ||||||
chr3:120630835
|
C | CACAT | 23 | a0001c0001t0001g0174a0001c0001t0001g0194a0001c0001t0001g0222others(20): Show | 23 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1189-2307_1189-230 others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630835 | ||||||
chr3:120630835
|
C | CAT | 7 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0095others(4): Show | 7 | HG01346.hp1 HG01928.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1189-2307_1189-230 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630835 | ||||||
chr3:120630835
|
C | T | 43 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(40): Show | 47 | HG00099.hp2 HG00280.hp1 HG01433.hp1 others(44): Show |
intron_variant | MODIFIER | c.1189-2306G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630835 | ||||||
chr3:120630837
|
C | T | 16 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0057others(13): Show | 16 | HG00621.hp2 HG01099.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1189-2308G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630837 | ||||||
chr3:120630839
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1188+2308G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630839 | ||||||
chr3:120630843
|
T | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(88): Show | 95 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1188+2304A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | ||||||
chr3:120630843
|
T | TAC | 18 | a0001c0001t0001g0051a0001c0001t0001g0061a0001c0001t0001g0080others(15): Show | 18 | HG00735.hp1 HG01071.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1188+2302_1188+230 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | ||||||
chr3:120630843
|
T | TACAC | 9 | a0001c0001t0001g0014a0001c0001t0001g0056a0001c0001t0001g0117others(6): Show | 10 | HG01099.hp2 HG02027.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.1188+2300_1188+230 others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | ||||||
chr3:120630843
|
T | TACACACA others(3): Show |
4 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(1): Show | 4 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1188+2294_1188+230 others(14): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | ||||||
chr3:120630843
|
TAC | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.1188+2302_1188+230 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | ||||||
chr3:120630843
|
TACAC | T | 20 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0066others(17): Show | 22 | HG00558.hp2 HG00639.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1188+2300_1188+230 others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | ||||||
chr3:120630843
|
TACACAC | T | 6 | a0001c0001t0001g0033a0001c0001t0001g0136a0001c0001t0001g0210others(3): Show | 6 | HG02280.hp2 HG02523.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+2298_1188+230 others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | ||||||
chr3:120630845
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1188+2302G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630845 | ||||||
chr3:120630847
|
C | T | 72 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(69): Show | 76 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1188+2300G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630847 | ||||||
chr3:120630849
|
C | T | 13 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0057others(10): Show | 13 | HG01099.hp1 HG01109.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1188+2298G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630849 | ||||||
chr3:120630851
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1188+2296G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630851 | ||||||
chr3:120630859
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1188+2288G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630859 | ||||||
chr3:120630874
|
A | G | 5 | a0001c0001t0001g0057a0001c0001t0001g0071a0003c0005t0001g0028others(2): Show | 5 | HG01099.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1188+2273T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630874 | ||||||
chr3:120630937
|
C | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0040others(9): Show | 12 | HG00735.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1188+2210G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630937 | ||||||
chr3:120630940
|
C | T | 9 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0344others(6): Show | 9 | HG02559.hp1 HG02922.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1188+2207G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630940 | ||||||
chr3:120630961
|
T | C | 8 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0051others(5): Show | 8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1188+2186A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630961 | ||||||
chr3:120631399
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0225 | 2 | HG02148.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1188+1748C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631399 | ||||||
chr3:120631451
|
C | A | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1188+1696G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631451 | ||||||
chr3:120631481
|
CTTA | C | 40 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0074others(37): Show | 45 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1188+1663_1188+166 others(7): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631481 | ||||||
chr3:120631570
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1188+1577G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631570 | ||||||
chr3:120631658
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0073 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1188+1489T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631658 | ||||||
chr3:120631790
|
A | C | 1 | a0001c0001t0001g0234 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1188+1357T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631790 | ||||||
chr3:120631897
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1188+1250G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631897 | ||||||
chr3:120631978
|
C | T | 6 | a0001c0003t0001g0058a0001c0003t0001g0070a0001c0003t0001g0088others(3): Show | 6 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1188+1169G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631978 | ||||||
chr3:120632031
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1188+1116C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632031 | ||||||
chr3:120632078
|
T | C | 2 | a0001c0001t0001g0147a0002c0002t0001g0317 | 2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1188+1069A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632078 | ||||||
chr3:120632086
|
C | T | 6 | a0001c0003t0001g0058a0001c0003t0001g0070a0001c0003t0001g0088others(3): Show | 6 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1188+1061G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632086 | ||||||
chr3:120632089
|
C | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0051others(5): Show | 8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1188+1058G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632089 | ||||||
chr3:120632151
|
C | G | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1188+996G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632151 | ||||||
chr3:120632448
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1188+699T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632448 | ||||||
chr3:120632503
|
G | A | 1 | a0002c0002t0001g0260 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1188+644C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632503 | ||||||
chr3:120632504
|
C | T | 1 | a0002c0002t0001g0260 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1188+643G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632504 | ||||||
chr3:120632616
|
C | T | 1 | a0002c0002t0001g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1188+531G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632616 | ||||||
chr3:120632764
|
A | C | 11 | a0001c0003t0001g0058a0001c0003t0001g0070a0001c0003t0001g0088others(8): Show | 11 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.1188+383T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632764 | ||||||
chr3:120632768
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1188+379C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632768 | ||||||
chr3:120632778
|
G | A | 14 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0150others(11): Show | 14 | HG00609.hp2 HG00621.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1188+369C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632778 | ||||||
chr3:120632787
|
G | T | 1 | a0001c0001t0001g0242 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1188+360C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632787 | ||||||
chr3:120632804
|
C | T | 4 | a0002c0002t0001g0289a0002c0002t0001g0290a0002c0002t0001g0304others(1): Show | 4 | HG01433.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1188+343G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632804 | ||||||
chr3:120632944
|
C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 81 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.1188+203G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632944 | ||||||
chr3:120633005
|
C | A | 66 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(63): Show | 68 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1188+142G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120633005 | ||||||
chr3:120633081
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1188+66C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120633081 | ||||||
chr3:120633096
|
T | C | 23 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0040others(20): Show | 23 | HG00735.hp1 HG01106.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.1188+51A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120633096 | ||||||
chr3:120633118
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1188+29G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120633118 | ||||||
chr3:120633679
|
G | A | 1 | a0002c0002t0001g0323 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1007-351C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120633679 | ||||||
chr3:120633719
|
C | T | 11 | a0001c0003t0001g0058a0001c0003t0001g0070a0001c0003t0001g0088others(8): Show | 11 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007-391G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120633719 | ||||||
chr3:120633796
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0341others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-468C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120633796 | ||||||
chr3:120633863
|
C | T | 1 | a0002c0002t0001g0274 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1007-535G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120633863 | ||||||
chr3:120633942
|
CTTCTA | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0001g0151others(1): Show | 5 | NA18957.hp1 NA18995.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007-619_1007-615d others(7): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120633942 | ||||||
chr3:120634053
|
C | G | 31 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0063others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1007-725G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634053 | ||||||
chr3:120634123
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1007-795G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634123 | ||||||
chr3:120634129
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0341others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-801C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634129 | ||||||
chr3:120634167
|
C | T | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007-839G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634167 | ||||||
chr3:120634250
|
T | C | 3 | a0001c0001t0001g0006a0002c0002t0001g0261a0002c0002t0001g0262 | 4 | HG00639.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007-922A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634250 | ||||||
chr3:120634368
|
C | A | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(221): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1007-1040G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634368 | ||||||
chr3:120634551
|
A | G | 1 | a0002c0002t0001g0182 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1007-1223T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634551 | ||||||
chr3:120634694
|
G | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1007-1366C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634694 | ||||||
chr3:120634896
|
A | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1007-1568T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634896 | ||||||
chr3:120635065
|
C | T | 6 | a0001c0003t0001g0058a0001c0003t0001g0070a0001c0003t0001g0088others(3): Show | 6 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1007-1737G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635065 | ||||||
chr3:120635367
|
C | T | 3 | a0001c0001t0001g0163a0002c0002t0001g0279a0002c0002t0001g0328 | 3 | NA18940.hp2 NA18961.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1007-2039G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635367 | ||||||
chr3:120635474
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1007-2146G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635474 | ||||||
chr3:120635476
|
C | CA | 6 | a0001c0001t0001g0151a0001c0001t0001g0163a0001c0001t0001g0190others(3): Show | 6 | HG03927.hp2 HG04184.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007-2149dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635476 | ||||||
chr3:120635476
|
CA | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1007-2149delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635476 | ||||||
chr3:120635476
|
CAA | C | 7 | a0001c0001t0001g0116a0001c0001t0001g0140a0001c0001t0001g0184others(4): Show | 7 | HG02896.hp1 HG02965.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1007-2150_1007-214 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635476 | ||||||
chr3:120635644
|
G | A | 11 | a0001c0003t0001g0058a0001c0003t0001g0070a0001c0003t0001g0088others(8): Show | 11 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007-2316C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635644 | ||||||
chr3:120635674
|
G | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0072 | 2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1007-2346C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635674 | ||||||
chr3:120635686
|
C | A | 1 | a0001c0001t0001g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1007-2358G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635686 | ||||||
chr3:120635928
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1006+2527T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635928 | ||||||
chr3:120636099
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1006+2356G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636099 | ||||||
chr3:120636116
|
C | CA | 32 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0060others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1006+2338dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636116 | ||||||
chr3:120636116
|
CA | C | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 213 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1006+2338delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636116 | ||||||
chr3:120636116
|
CAA | C | 20 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0040others(17): Show | 20 | HG00735.hp1 HG01891.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1006+2337_1006+233 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636116 | ||||||
chr3:120636125
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1006+2330T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636125 | ||||||
chr3:120636139
|
G | T | 45 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0025others(42): Show | 50 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1006+2316C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636139 | ||||||
chr3:120636162
|
C | G | 12 | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0001t0001g0144others(9): Show | 13 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.1006+2293G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636162 | ||||||
chr3:120636177
|
G | C | 8 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0051others(5): Show | 8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006+2278C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636177 | ||||||
chr3:120636184
|
C | T | 1 | a0002c0002t0001g0171 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1006+2271G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636184 | ||||||
chr3:120636280
|
C | CA | 15 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0123others(12): Show | 15 | HG00140.hp2 HG00673.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1006+2174dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636280 | ||||||
chr3:120636280
|
CA | C | 6 | a0001c0001t0001g0175a0001c0004t0001g0067a0001c0004t0001g0068others(3): Show | 6 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006+2174delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636280 | ||||||
chr3:120636518
|
C | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0051others(5): Show | 8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006+1937G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636518 | ||||||
chr3:120636522
|
C | T | 45 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0074others(42): Show | 50 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1006+1933G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636522 | ||||||
chr3:120636674
|
T | C | 3 | a0002c0002t0001g0276a0002c0002t0001g0277a0002c0002t0001g0278 | 3 | NA18986.hp1 NA19056.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1006+1781A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636674 | ||||||
chr3:120636757
|
T | C | 1 | a0002c0002t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1006+1698A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636757 | ||||||
chr3:120636872
|
G | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0074others(38): Show | 46 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1006+1583C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636872 | ||||||
chr3:120636948
|
G | C | 6 | a0001c0003t0001g0058a0001c0003t0001g0070a0001c0003t0001g0088others(3): Show | 6 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006+1507C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636948 | ||||||
chr3:120637214
|
A | G | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1006+1241T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637214 | ||||||
chr3:120637224
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1006+1231G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637224 | ||||||
chr3:120637257
|
T | G | 1 | a0002c0002t0001g0306 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1006+1198A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637257 | ||||||
chr3:120637307
|
G | GA | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1006+1147dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637307 | ||||||
chr3:120637307
|
G | GAA | 8 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0107others(5): Show | 8 | HG00639.hp2 HG00673.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006+1146_1006+114 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637307 | ||||||
chr3:120637307
|
GAA | G | 19 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0051others(16): Show | 19 | HG00735.hp1 HG01106.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.1006+1146_1006+114 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637307 | ||||||
chr3:120637385
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1006+1070A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637385 | ||||||
chr3:120637600
|
GTCTCTCT others(5): Show |
G | 11 | a0001c0003t0001g0058a0001c0003t0001g0070a0001c0003t0001g0088others(8): Show | 11 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.1006+843_1006+854d others(14): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637600 | ||||||
chr3:120637610
|
CTCTCTCT others(3): Show |
C | 3 | a0001c0001t0001g0040a0001c0001t0001g0061a0001c0001t0001g0085 | 3 | HG00735.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1006+835_1006+844d others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637610 | ||||||
chr3:120637701
|
A | G | 1 | a0002c0002t0001g0179 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1006+754T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637701 | ||||||
chr3:120637767
|
C | A | 35 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 38 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1006+688G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637767 | ||||||
chr3:120637890
|
A | C | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1006+565T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637890 | ||||||
chr3:120638099
|
C | T | 12 | a0001c0001t0001g0024a0001c0001t0001g0078a0001c0001t0001g0095others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1006+356G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120638099 | ||||||
chr3:120638142
|
T | C | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(221): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1006+313A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120638142 | ||||||
chr3:120638194
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1006+261G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120638194 | ||||||
chr3:120638255
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1006+200G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120638255 | ||||||
chr3:120638306
|
G | A | 1 | a0002c0002t0001g0259 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1006+149C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120638306 | ||||||
chr3:120638608
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.880-27G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120638608 | ||||||
chr3:120638611
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.880-30T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120638611 | ||||||
chr3:120638694
|
T | C | 7 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG00639.hp2 HG01081.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-113A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120638694 | ||||||
chr3:120638749
|
C | G | 1 | a0002c0002t0001g0166 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.880-168G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120638749 | ||||||
chr3:120639050
|
C | G | 2 | a0001c0001t0001g0195a0002c0002t0001g0284 | 2 | HG02015.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.880-469G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639050 | ||||||
chr3:120639114
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.880-533G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639114 | ||||||
chr3:120639466
|
G | A | 3 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | NA18948.hp1 NA18999.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.880-885C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639466 | ||||||
chr3:120639537
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.880-956A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639537 | ||||||
chr3:120639574
|
G | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0001g0056 | 3 | HG01891.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.880-993C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639574 | ||||||
chr3:120639856
|
AAAT | A | 3 | a0001c0003t0001g0058a0001c0003t0001g0070a0001c0003t0001g0088 | 3 | HG03195.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.880-1278_880-1276d others(5): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639856 | ||||||
chr3:120639910
|
AT | A | 3 | a0001c0003t0001g0058a0001c0003t0001g0070a0001c0003t0001g0088 | 3 | HG03195.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.880-1330delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639910 | ||||||
chr3:120639992
|
C | G | 1 | a0001c0001t0001g0011 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.880-1411G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639992 | ||||||
chr3:120639993
|
T | G | 1 | a0001c0001t0001g0011 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.880-1412A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639993 | ||||||
chr3:120640016
|
G | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0341others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-1435C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640016 | ||||||
chr3:120640121
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0341others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+1468C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640121 | ||||||
chr3:120640149
|
A | AGAAG | 16 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0079others(13): Show | 18 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.879+1436_879+1439d others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640149 | ||||||
chr3:120640179
|
C | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(63): Show | 68 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.879+1410G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640179 | ||||||
chr3:120640256
|
G | A | 1 | a0001c0001t0001g0021 | 2 | NA18983.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.879+1333C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640256 | ||||||
chr3:120640319
|
T | C | 3 | a0001c0001t0001g0006a0002c0002t0001g0261a0002c0002t0001g0262 | 4 | HG00639.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+1270A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640319 | ||||||
chr3:120640381
|
G | A | 5 | a0001c0001t0001g0148a0002c0002t0001g0018a0002c0002t0001g0298others(2): Show | 6 | HG00099.hp1 HG00140.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+1208C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640381 | ||||||
chr3:120640405
|
G | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(63): Show | 68 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.879+1184C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640405 | ||||||
chr3:120640412
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.879+1177C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640412 | ||||||
chr3:120640534
|
A | G | 1 | a0001c0001t0001g0337 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.879+1055T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640534 | ||||||
chr3:120640557
|
A | G | 1 | a0003c0005t0001g0031 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.879+1032T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640557 | ||||||
chr3:120640574
|
C | T | 62 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(59): Show | 64 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.879+1015G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640574 | ||||||
chr3:120640622
|
G | A | 7 | a0001c0003t0001g0058a0001c0003t0001g0070a0001c0004t0001g0067others(4): Show | 7 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+967C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640622 | ||||||
chr3:120640877
|
G | C | 15 | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0001t0001g0144others(12): Show | 16 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.879+712C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640877 | ||||||
chr3:120640966
|
C | T | 2 | a0001c0003t0001g0058a0001c0003t0001g0070 | 2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.879+623G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640966 | ||||||
chr3:120640998
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.879+591A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640998 | ||||||
chr3:120641029
|
G | C | 74 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0033others(71): Show | 76 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.879+560C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641029 | ||||||
chr3:120641085
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0081a0002c0002t0001g0253 | 3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.879+504G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641085 | ||||||
chr3:120641164
|
C | T | 65 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(62): Show | 67 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.879+425G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641164 | ||||||
chr3:120641265
|
C | T | 1 | a0002c0002t0001g0330 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.879+324G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641265 | ||||||
chr3:120641484
|
T | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.879+105A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641484 | ||||||
chr3:120641525
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.879+64A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641525 | ||||||
chr3:120641571
|
T | C | 1 | a0002c0002t0001g0283 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.879+18A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641571 | ||||||
chr3:120641889
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.775-196G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120641889 | ||||||
chr3:120641984
|
T | G | 1 | a0001c0001t0001g0008 | 2 | HG00099.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.775-291A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120641984 | ||||||
chr3:120642009
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.775-316T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642009 | ||||||
chr3:120642106
|
C | T | 1 | a0002c0002t0001g0289 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.775-413G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642106 | ||||||
chr3:120642178
|
A | G | 1 | a0002c0002t0001g0343 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.775-485T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642178 | ||||||
chr3:120642218
|
T | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0062a0001c0001t0001g0086others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-525A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642218 | ||||||
chr3:120642229
|
T | C | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.775-536A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642229 | ||||||
chr3:120642462
|
A | G | 1 | a0001c0003t0001g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.775-769T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642462 | ||||||
chr3:120642478
|
G | T | 1 | a0002c0002t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.775-785C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642478 | ||||||
chr3:120642544
|
T | TGACATAT others(4): Show |
1 | a0001c0001t0001g0130 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.775-862_775-852dup others(11): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642544 | ||||||
chr3:120642642
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.775-949T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642642 | ||||||
chr3:120642682
|
C | G | 1 | a0002c0002t0001g0247 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.775-989G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642682 | ||||||
chr3:120642764
|
C | G | 4 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0341others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-1071G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642764 | ||||||
chr3:120642805
|
C | T | 1 | a0002c0002t0001g0168 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.775-1112G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642805 | ||||||
chr3:120642887
|
C | G | 1 | a0001c0001t0001g0005 | 2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.775-1194G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642887 | ||||||
chr3:120642977
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.775-1284G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642977 | ||||||
chr3:120643050
|
G | A | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+1269C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643050 | ||||||
chr3:120643057
|
A | G | 4 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0341others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+1262T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643057 | ||||||
chr3:120643163
|
G | A | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0112others(1): Show | 4 | HG00738.hp2 HG00741.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+1156C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643163 | ||||||
chr3:120643167
|
G | A | 48 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0074others(45): Show | 53 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.774+1152C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643167 | ||||||
chr3:120643417
|
C | A | 1 | a0001c0001t0001g0211 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.774+902G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643417 | ||||||
chr3:120643474
|
C | G | 48 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0074others(45): Show | 53 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.774+845G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643474 | ||||||
chr3:120643575
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0073 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.774+744A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643575 | ||||||
chr3:120644014
|
A | G | 65 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(62): Show | 67 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.774+305T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120644014 | ||||||
chr3:120644116
|
G | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(89): Show | 99 | HG00323.hp2 HG00639.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.774+203C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120644116 | ||||||
chr3:120644153
|
A | C | 1 | a0001c0001t0001g0100 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.774+166T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120644153 | ||||||
chr3:120644201
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.774+118C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120644201 | ||||||
chr3:120644233
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.774+86A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120644233 | ||||||
chr3:120644481
|
C | CA | 5 | a0002c0002t0001g0246a0002c0002t0001g0250a0002c0002t0001g0271others(2): Show | 5 | NA18941.hp1 NA19011.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.650-39dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644481 | ||||||
chr3:120644496
|
A | G | 1 | a0002c0002t0001g0326 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.650-53T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644496 | ||||||
chr3:120644528
|
T | C | 22 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0021others(19): Show | 25 | HG02015.hp2 HG02129.hp1 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.650-85A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644528 | ||||||
chr3:120644622
|
G | A | 1 | a0002c0002t0001g0343 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.650-179C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644622 | ||||||
chr3:120644676
|
T | A | 1 | a0002c0002t0001g0259 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.650-233A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644676 | ||||||
chr3:120644863
|
A | G | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.650-420T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644863 | ||||||
chr3:120644893
|
CT | C | 65 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(62): Show | 67 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.650-451delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644893 | ||||||
chr3:120644926
|
T | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(17): Show | 22 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.650-483A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644926 | ||||||
chr3:120645160
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.650-717T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120645160 | ||||||
chr3:120645294
|
G | A | 48 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0074others(45): Show | 53 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.650-851C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120645294 | ||||||
chr3:120645460
|
A | T | 34 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0057others(31): Show | 37 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(34): Show |
intron_variant | MODIFIER | c.649+807T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120645460 | ||||||
chr3:120645464
|
C | A | 1 | a0001c0001t0001g0011 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.649+803G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120645464 | ||||||
chr3:120645599
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.649+668A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120645599 | ||||||
chr3:120646073
|
T | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0073 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.649+194A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120646073 | ||||||
chr3:120646163
|
G | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 66 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.649+104C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120646163 | ||||||
chr3:120646182
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0341others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.649+85C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120646182 | ||||||
chr3:120646208
|
T | C | 1 | a0001c0001t0001g0007 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.649+59A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120646208 | ||||||
chr3:120646656
|
T | TA | 49 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0074others(46): Show | 54 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.550-291dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 8/13 | chr3 | 120646656 | ||||||
chr3:120646692
|
G | A | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.549+281C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 8/13 | chr3 | 120646692 | ||||||
chr3:120646784
|
T | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(63): Show | 68 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.549+189A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 8/13 | chr3 | 120646784 | ||||||
chr3:120647215
|
A | G | 8 | a0001c0001t0001g0124a0001c0001t0001g0158a0002c0002t0001g0166others(5): Show | 8 | HG00609.hp2 HG02074.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-163T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647215 | ||||||
chr3:120647263
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0203 | 2 | HG02074.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.470-211C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647263 | ||||||
chr3:120647314
|
A | AG | 4 | a0001c0001t0001g0026a0001c0001t0001g0151a0001c0001t0001g0153others(1): Show | 4 | HG01243.hp1 HG02055.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-263dupC | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647314 | ||||||
chr3:120647341
|
C | T | 1 | a0002c0002t0001g0294 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.470-289G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647341 | ||||||
chr3:120647391
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.470-339A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647391 | ||||||
chr3:120647395
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.470-343G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647395 | ||||||
chr3:120647675
|
CA | C | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+201delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647675 | ||||||
chr3:120648056
|
C | T | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0003t0001g0177 | 3 | HG02922.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.435-145G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648056 | ||||||
chr3:120648232
|
G | T | 284 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.435-321C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648232 | ||||||
chr3:120648364
|
G | A | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-453C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648364 | ||||||
chr3:120648382
|
G | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0081a0002c0002t0001g0253 | 3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.435-471C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648382 | ||||||
chr3:120648476
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0001g0056 | 3 | HG01891.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.435-565G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648476 | ||||||
chr3:120648555
|
G | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(63): Show | 68 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.435-644C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648555 | ||||||
chr3:120648666
|
T | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0341others(6): Show | 9 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.435-755A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648666 | ||||||
chr3:120648799
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0073 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.435-888G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648799 | ||||||
chr3:120648838
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.435-927A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648838 | ||||||
chr3:120648933
|
G | A | 1 | a0001c0003t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.435-1022C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648933 | ||||||
chr3:120648958
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0081a0002c0002t0001g0253 | 3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.435-1047C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648958 | ||||||
chr3:120648972
|
C | T | 35 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0057others(32): Show | 38 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(35): Show |
intron_variant | MODIFIER | c.435-1061G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648972 | ||||||
chr3:120649139
|
C | CT | 7 | a0001c0001t0001g0112a0001c0001t0001g0153a0001c0001t0001g0161others(4): Show | 7 | HG01243.hp1 HG02258.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.435-1229dupA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649139 | ||||||
chr3:120649139
|
CT | C | 8 | a0001c0001t0001g0095a0001c0001t0001g0126a0001c0001t0001g0186others(5): Show | 8 | HG02735.hp1 HG03491.hp2 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.435-1229delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649139 | ||||||
chr3:120649139
|
CTT | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.435-1230_435-1229d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649139 | ||||||
chr3:120649143
|
T | C | 1 | a0002c0002t0001g0323 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.435-1232A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649143 | ||||||
chr3:120649144
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.435-1233A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649144 | ||||||
chr3:120649175
|
C | A | 2 | a0001c0003t0001g0058a0001c0003t0001g0070 | 2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.435-1264G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649175 | ||||||
chr3:120649186
|
G | A | 1 | a0005c0012t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.435-1275C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649186 | ||||||
chr3:120649229
|
G | A | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-1318C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649229 | ||||||
chr3:120649231
|
C | T | 62 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(59): Show | 64 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.435-1320G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649231 | ||||||
chr3:120649286
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.435-1375C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649286 | ||||||
chr3:120649353
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(203): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.434+1421A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649353 | ||||||
chr3:120649423
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.434+1351C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649423 | ||||||
chr3:120649438
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(31): Show | 38 | HG00639.hp1 HG01175.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.434+1336G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649438 | ||||||
chr3:120649625
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0081a0002c0002t0001g0253 | 3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.434+1149G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649625 | ||||||
chr3:120649638
|
G | A | 2 | a0002c0002t0001g0324a0002c0002t0001g0325 | 2 | NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.434+1136C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649638 | ||||||
chr3:120649674
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.434+1100G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649674 | ||||||
chr3:120649675
|
C | A | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+1099G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649675 | ||||||
chr3:120649738
|
G | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(200): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.434+1036C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649738 | ||||||
chr3:120649824
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.434+950C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649824 | ||||||
chr3:120649952
|
C | G | 1 | a0001c0003t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.434+822G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649952 | ||||||
chr3:120650003
|
A | T | 1 | a0001c0003t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.434+771T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650003 | ||||||
chr3:120650014
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0341others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+760C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650014 | ||||||
chr3:120650047
|
T | C | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+727A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650047 | ||||||
chr3:120650048
|
A | T | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+726T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650048 | ||||||
chr3:120650418
|
C | T | 1 | a0002c0002t0001g0308 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.434+356G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650418 | ||||||
chr3:120650490
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0191 | 2 | HG00323.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.434+284G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650490 | ||||||
chr3:120650491
|
G | A | 1 | a0001c0001t0001g0344 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.434+283C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650491 | ||||||
chr3:120650503
|
C | T | 1 | a0002c0002t0001g0257 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.434+271G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650503 | ||||||
chr3:120650728
|
T | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(200): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.434+46A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650728 | ||||||
chr3:120650876
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.343-11G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120650876 | ||||||
chr3:120651390
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.343-525A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651390 | ||||||
chr3:120651427
|
C | T | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-562G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651427 | ||||||
chr3:120651545
|
T | C | 36 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0057others(33): Show | 39 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.343-680A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651545 | ||||||
chr3:120651793
|
T | C | 1 | a0001c0006t0001g0015 | 2 | HG01192.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.342+799A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651793 | ||||||
chr3:120651801
|
C | T | 69 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(66): Show | 71 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.342+791G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651801 | ||||||
chr3:120651807
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.342+785T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651807 | ||||||
chr3:120651857
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0081a0002c0002t0001g0253 | 3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.342+735C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651857 | ||||||
chr3:120651979
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.342+613C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651979 | ||||||
chr3:120652071
|
G | A | 1 | a0001c0004t0001g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.342+521C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652071 | ||||||
chr3:120652143
|
G | A | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+449C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652143 | ||||||
chr3:120652335
|
TTAAG | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0074others(44): Show | 52 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.342+253_342+256del others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652335 | ||||||
chr3:120652360
|
A | G | 1 | a0002c0002t0001g0291 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.342+232T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652360 | ||||||
chr3:120652522
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0013others(89): Show | 101 | HG00280.hp2 HG00558.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.342+70C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652522 | ||||||
chr3:120652567
|
G | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(283): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.342+25C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652567 | ||||||
chr3:120652570
|
G | T | 1 | a0002c0002t0001g0275 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.342+22C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652570 | ||||||
chr3:120652655
|
G | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0042 | 3 | HG03041.hp1 HG03486.hp1 NA18522.hp2 |
splice_region_variant&intron_variant | LOW | c.283-4C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652655 | ||||||
chr3:120652674
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.283-23C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652674 | ||||||
chr3:120652683
|
C | T | 1 | a0002c0002t0001g0283 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.283-32G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652683 | ||||||
chr3:120652796
|
A | G | 71 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0035others(68): Show | 73 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.283-145T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652796 | ||||||
chr3:120652796
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.283-145T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652796 | ||||||
chr3:120652942
|
T | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.283-291A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652942 | ||||||
chr3:120652990
|
G | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0081a0002c0002t0001g0253 | 3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283-339C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652990 | ||||||
chr3:120653108
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.283-457G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653108 | ||||||
chr3:120653192
|
G | A | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-541C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653192 | ||||||
chr3:120653279
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.283-628A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653279 | ||||||
chr3:120653401
|
G | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0341others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-750C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653401 | ||||||
chr3:120653474
|
G | A | 9 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0051others(6): Show | 9 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-823C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653474 | ||||||
chr3:120653491
|
G | T | 1 | a0002c0002t0001g0331 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.283-840C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653491 | ||||||
chr3:120653504
|
G | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(74): Show | 84 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.283-853C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653504 | ||||||
chr3:120653693
|
G | T | 63 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(60): Show | 65 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.283-1042C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653693 | ||||||
chr3:120654013
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.283-1362G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654013 | ||||||
chr3:120654130
|
G | A | 1 | a0001c0003t0001g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.283-1479C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654130 | ||||||
chr3:120654191
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.283-1540T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654191 | ||||||
chr3:120654336
|
T | C | 2 | a0001c0001t0001g0121a0001c0003t0001g0122 | 2 | HG01934.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.283-1685A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654336 | ||||||
chr3:120654389
|
G | A | 2 | a0001c0001t0002g0022a0002c0002t0001g0270 | 2 | HG01109.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.283-1738C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654389 | ||||||
chr3:120654438
|
A | G | 1 | a0001c0001t0001g0344 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.283-1787T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654438 | ||||||
chr3:120654497
|
T | C | 2 | a0001c0001t0001g0341a0001c0001t0001g0342 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.283-1846A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654497 | ||||||
chr3:120654541
|
A | C | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0003t0001g0177 | 3 | HG02922.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.283-1890T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654541 | ||||||
chr3:120654613
|
C | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0341others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-1962G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654613 | ||||||
chr3:120654840
|
A | G | 2 | a0001c0001t0001g0081a0002c0002t0001g0253 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283-2189T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654840 | ||||||
chr3:120654948
|
G | T | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.283-2297C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654948 | ||||||
chr3:120655039
|
C | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283-2388G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655039 | ||||||
chr3:120655049
|
T | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.283-2398A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655049 | ||||||
chr3:120655095
|
C | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(15): Show | 20 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.283-2444G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655095 | ||||||
chr3:120655138
|
G | T | 2 | a0002c0007t0001g0256a0002c0007t0001g0321 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.283-2487C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655138 | ||||||
chr3:120655167
|
G | T | 1 | a0001c0001t0001g0190 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283-2516C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655167 | ||||||
chr3:120655192
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.283-2541A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655192 | ||||||
chr3:120655261
|
G | A | 1 | a0001c0003t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.283-2610C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655261 | ||||||
chr3:120655358
|
C | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.283-2707G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655358 | ||||||
chr3:120655370
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283-2719G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655370 | ||||||
chr3:120655482
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.283-2831T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655482 | ||||||
chr3:120655597
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283-2946A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655597 | ||||||
chr3:120655623
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0341others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-2972C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655623 | ||||||
chr3:120655761
|
T | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(83): Show | 93 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.283-3110A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655761 | ||||||
chr3:120655799
|
T | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.283-3148A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655799 | ||||||
chr3:120655863
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(78): Show | 88 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.283-3212G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655863 | ||||||
chr3:120655864
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.283-3213T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655864 | ||||||
chr3:120656052
|
C | G | 64 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0100others(61): Show | 66 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.283-3401G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656052 | ||||||
chr3:120656133
|
T | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(83): Show | 93 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.283-3482A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656133 | ||||||
chr3:120656214
|
C | T | 1 | a0002c0002t0001g0275 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.283-3563G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656214 | ||||||
chr3:120656247
|
A | T | 2 | a0001c0001t0001g0174a0002c0002t0001g0339 | 2 | HG02683.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.283-3596T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656247 | ||||||
chr3:120656361
|
T | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.283-3710A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656361 | ||||||
chr3:120656366
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.283-3715A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656366 | ||||||
chr3:120656376
|
G | T | 1 | a0001c0001t0001g0233 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.283-3725C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656376 | ||||||
chr3:120656519
|
A | G | 4 | a0002c0002t0001g0169a0002c0002t0001g0255a0002c0002t0001g0265others(1): Show | 4 | HG00597.hp1 HG00621.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-3868T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656519 | ||||||
chr3:120656563
|
T | TG | 141 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.283-3913dupC | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656563 | ||||||
chr3:120656565
|
G | C | 1 | a0001c0001t0001g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283-3914C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656565 | ||||||
chr3:120656582
|
C | T | 2 | a0001c0001t0001g0174a0002c0002t0001g0339 | 2 | HG02683.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.283-3931G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656582 | ||||||
chr3:120656603
|
G | C | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.283-3952C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656603 | ||||||
chr3:120656613
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.283-3962C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656613 | ||||||
chr3:120656706
|
C | T | 71 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(68): Show | 74 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.283-4055G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656706 | ||||||
chr3:120656712
|
C | A | 1 | a0002c0002t0001g0320 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.283-4061G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656712 | ||||||
chr3:120656763
|
G | A | 2 | a0002c0007t0001g0256a0002c0007t0001g0321 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.283-4112C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656763 | ||||||
chr3:120656932
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0034others(7): Show | 11 | HG01891.hp1 HG02109.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.283-4281C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656932 | ||||||
chr3:120657004
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.283-4353C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657004 | ||||||
chr3:120657168
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283-4517C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657168 | ||||||
chr3:120657537
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0034others(7): Show | 11 | HG01891.hp1 HG02109.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.283-4886A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657537 | ||||||
chr3:120657548
|
G | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.283-4897C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657548 | ||||||
chr3:120657584
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0081a0002c0002t0001g0253 | 3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283-4933G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657584 | ||||||
chr3:120657812
|
C | G | 1 | a0001c0001t0001g0232 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.283-5161G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657812 | ||||||
chr3:120657818
|
TGA | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.283-5169_283-5168d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657818 | ||||||
chr3:120657825
|
GAGAGAGA others(7): Show |
G | 1 | a0001c0001t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.283-5188_283-5175d others(16): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657825 | ||||||
chr3:120657899
|
C | T | 15 | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0001t0001g0144others(12): Show | 16 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.283-5248G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657899 | ||||||
chr3:120657943
|
C | G | 9 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0051others(6): Show | 9 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-5292G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657943 | ||||||
chr3:120657981
|
A | C | 46 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0074others(43): Show | 51 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.283-5330T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657981 | ||||||
chr3:120658018
|
A | G | 1 | a0002c0002t0001g0283 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.283-5367T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658018 | ||||||
chr3:120658274
|
G | A | 37 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0057others(34): Show | 40 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.283-5623C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658274 | ||||||
chr3:120658292
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.283-5641A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658292 | ||||||
chr3:120658349
|
G | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.283-5698C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658349 | ||||||
chr3:120658394
|
C | A | 1 | a0002c0002t0001g0340 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.283-5743G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658394 | ||||||
chr3:120658394
|
C | G | 2 | a0001c0001t0001g0124a0002c0002t0001g0172 | 2 | NA19010.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.283-5743G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658394 | ||||||
chr3:120658440
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0036others(23): Show | 29 | HG00639.hp1 HG01175.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.283-5789C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658440 | ||||||
chr3:120658520
|
A | G | 4 | a0002c0002t0001g0309a0002c0002t0001g0310a0002c0002t0001g0311others(1): Show | 4 | NA18956.hp2 NA18957.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-5869T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658520 | ||||||
chr3:120658582
|
A | T | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | NA18941.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.283-5931T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658582 | ||||||
chr3:120658603
|
T | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(79): Show | 89 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.283-5952A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658603 | ||||||
chr3:120658644
|
C | T | 1 | a0002c0002t0001g0271 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.283-5993G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658644 | ||||||
chr3:120658721
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0220 | 3 | HG02523.hp2 NA18988.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.283-6070C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658721 | ||||||
chr3:120658920
|
T | A | 79 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(76): Show | 82 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.283-6269A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658920 | ||||||
chr3:120658973
|
C | T | 1 | a0002c0002t0001g0270 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.283-6322G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658973 | ||||||
chr3:120658987
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.283-6336G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658987 | ||||||
chr3:120659096
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.283-6445G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659096 | ||||||
chr3:120659114
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0013others(94): Show | 106 | HG00280.hp2 HG00558.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.283-6463A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659114 | ||||||
chr3:120659125
|
A | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.283-6474T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659125 | ||||||
chr3:120659251
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.283-6600A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659251 | ||||||
chr3:120659408
|
G | A | 1 | a0001c0001t0001g0021 | 2 | NA18983.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.283-6757C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659408 | ||||||
chr3:120659420
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.283-6769G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659420 | ||||||
chr3:120659604
|
A | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.283-6953T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659604 | ||||||
chr3:120659723
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.283-7072G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659723 | ||||||
chr3:120659743
|
G | A | 3 | a0001c0001t0001g0057a0003c0005t0001g0028a0003c0005t0001g0032 | 3 | HG01099.hp1 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283-7092C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659743 | ||||||
chr3:120659879
|
TC | T | 8 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0051others(5): Show | 8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-7229delG | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659879 | ||||||
chr3:120659934
|
AAG | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0074others(37): Show | 44 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.283-7285_283-7284d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659934 | ||||||
chr3:120659936
|
GA | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0145others(1): Show | 4 | HG01106.hp2 HG01169.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-7286delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659936 | ||||||
chr3:120659938
|
GA | G | 16 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0065others(13): Show | 19 | HG00558.hp2 HG01070.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.283-7288delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659938 | ||||||
chr3:120659939
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0145others(6): Show | 9 | HG00673.hp1 HG01106.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-7288T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659939 | ||||||
chr3:120659941
|
A | C | 8 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0051others(5): Show | 8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-7290T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659941 | ||||||
chr3:120659941
|
A | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(67): Show | 77 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.283-7290T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659941 | ||||||
chr3:120659943
|
T | G | 82 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(79): Show | 89 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.283-7292A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659943 | ||||||
chr3:120659944
|
G | A | 9 | a0001c0001t0001g0124a0001c0001t0001g0150a0001c0001t0001g0158others(6): Show | 9 | HG00609.hp2 HG02074.hp2 NA18982.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-7293C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659944 | ||||||
chr3:120659947
|
G | C | 10 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0051others(7): Show | 10 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-7296C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659947 | ||||||
chr3:120659968
|
G | A | 2 | a0001c0003t0001g0058a0001c0003t0001g0070 | 2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.283-7317C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659968 | ||||||
chr3:120659980
|
A | T | 1 | a0001c0001t0001g0200 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.283-7329T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659980 | ||||||
chr3:120660114
|
C | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0079others(13): Show | 18 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.283-7463G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660114 | ||||||
chr3:120660129
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.283-7478T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660129 | ||||||
chr3:120660505
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.283-7854A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660505 | ||||||
chr3:120660550
|
C | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0081a0002c0002t0001g0253 | 3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283-7899G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660550 | ||||||
chr3:120660556
|
G | A | 1 | a0002c0002t0001g0020 | 2 | NA18942.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.283-7905C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660556 | ||||||
chr3:120660558
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0081a0002c0002t0001g0253 | 3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283-7907A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660558 | ||||||
chr3:120660588
|
G | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(79): Show | 89 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.283-7937C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660588 | ||||||
chr3:120660623
|
G | A | 1 | a0002c0002t0001g0264 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.283-7972C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660623 | ||||||
chr3:120660744
|
G | C | 5 | a0001c0004t0001g0067a0001c0004t0001g0068a0001c0004t0001g0076others(2): Show | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-8093C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660744 | ||||||
chr3:120660873
|
GAAAACTT others(14): Show |
G | 1 | a0006c0011t0001g0041 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.283-8243_283-8223d others(23): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660873 | ||||||
chr3:120660895
|
C | G | 1 | a0006c0011t0001g0041 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.283-8244G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660895 | ||||||
chr3:120660950
|
C | T | 1 | a0001c0001t0001g0344 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.283-8299G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660950 | ||||||
chr3:120660989
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.283-8338A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660989 | ||||||
chr3:120661156
|
C | T | 78 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(75): Show | 81 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.283-8505G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661156 | ||||||
chr3:120661327
|
C | T | 8 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0051others(5): Show | 8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-8676G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661327 | ||||||
chr3:120661549
|
C | G | 1 | a0001c0001t0001g0033 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.282+8878G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661549 | ||||||
chr3:120661656
|
C | A | 2 | a0001c0003t0001g0058a0001c0003t0001g0070 | 2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.282+8771G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661656 | ||||||
chr3:120661667
|
C | T | 79 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(76): Show | 82 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.282+8760G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661667 | ||||||
chr3:120661672
|
AGCGCCAA others(7): Show |
A | 1 | a0001c0001t0001g0134 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.282+8741_282+8754d others(16): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661672 | ||||||
chr3:120661675
|
G | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.282+8752C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661675 | ||||||
chr3:120662014
|
C | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(79): Show | 89 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.282+8413G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662014 | ||||||
chr3:120662015
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(131): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.282+8412C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662015 | ||||||
chr3:120662082
|
C | T | 1 | a0002c0002t0001g0307 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.282+8345G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662082 | ||||||
chr3:120662248
|
G | A | 82 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(79): Show | 89 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.282+8179C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662248 | ||||||
chr3:120662277
|
C | T | 28 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(25): Show | 30 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.282+8150G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662277 | ||||||
chr3:120662328
|
A | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.282+8099T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662328 | ||||||
chr3:120662735
|
G | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.282+7692C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662735 | ||||||
chr3:120662769
|
C | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.282+7658G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662769 | ||||||
chr3:120663049
|
G | A | 79 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(76): Show | 82 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.282+7378C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663049 | ||||||
chr3:120663153
|
A | C | 29 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0104others(26): Show | 32 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.282+7274T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663153 | ||||||
chr3:120663167
|
G | T | 2 | a0001c0001t0001g0124a0002c0002t0001g0172 | 2 | NA19010.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.282+7260C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663167 | ||||||
chr3:120663253
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.282+7174G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663253 | ||||||
chr3:120663393
|
A | G | 63 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0033others(60): Show | 68 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.282+7034T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663393 | ||||||
chr3:120663494
|
C | T | 122 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0012others(119): Show | 129 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.282+6933G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663494 | ||||||
chr3:120663516
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0081a0002c0002t0001g0253 | 3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.282+6911C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663516 | ||||||
chr3:120663518
|
G | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(14): Show | 19 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.282+6909C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663518 | ||||||
chr3:120663625
|
C | G | 1 | a0002c0002t0001g0296 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.282+6802G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663625 | ||||||
chr3:120663639
|
A | G | 63 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0033others(60): Show | 68 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.282+6788T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663639 | ||||||
chr3:120663695
|
G | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0341others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+6732C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663695 | ||||||
chr3:120663779
|
T | TTG | 296 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.282+6647_282+6648i others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663779 | ||||||
chr3:120663800
|
TTATAA | T | 49 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0074others(46): Show | 54 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.282+6622_282+6626d others(7): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663800 | ||||||
chr3:120663851
|
G | GA | 26 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0036others(23): Show | 29 | HG00639.hp1 HG01175.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.282+6575dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663851 | ||||||
chr3:120663941
|
AT | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.282+6485delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663941 | ||||||
chr3:120664226
|
G | A | 1 | a0002c0002t0001g0167 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.282+6201C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664226 | ||||||
chr3:120664426
|
C | CT | 52 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0013others(49): Show | 59 | HG00323.hp1 HG01074.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.282+6000dupA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664426 | ||||||
chr3:120664426
|
C | CTT | 82 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(79): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.282+5999_282+6000d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664426 | ||||||
chr3:120664426
|
CT | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(84): Show | 92 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.282+6000delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664426 | ||||||
chr3:120664426
|
CTT | C | 8 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(5): Show | 8 | HG00639.hp2 HG01081.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+5999_282+6000d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664426 | ||||||
chr3:120664581
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.282+5846G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664581 | ||||||
chr3:120664630
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0001g0056 | 3 | HG01891.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.282+5797A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664630 | ||||||
chr3:120664676
|
T | C | 47 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0074others(44): Show | 52 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.282+5751A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664676 | ||||||
chr3:120665032
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0081a0002c0002t0001g0253 | 3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.282+5395A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665032 | ||||||
chr3:120665086
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.282+5341C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665086 | ||||||
chr3:120665325
|
C | T | 4 | a0001c0001t0001g0040a0001c0001t0001g0061a0001c0001t0001g0085others(1): Show | 4 | HG00735.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+5102G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665325 | ||||||
chr3:120665434
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.282+4993A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665434 | ||||||
chr3:120665463
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(97): Show | 110 | HG00280.hp2 HG00558.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.282+4964A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665463 | ||||||
chr3:120665466
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0144a0001c0001t0001g0338 | 3 | HG00323.hp1 HG01169.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.282+4961C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665466 | ||||||
chr3:120665468
|
T | C | 6 | a0001c0003t0001g0088a0001c0004t0001g0067a0001c0004t0001g0068others(3): Show | 6 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+4959A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665468 | ||||||
chr3:120665495
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(103): Show | 116 | HG00280.hp2 HG00558.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.282+4932G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665495 | ||||||
chr3:120665589
|
C | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(19): Show | 24 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.282+4838G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665589 | ||||||
chr3:120665599
|
G | C | 3 | a0001c0001t0001g0337a0001c0003t0001g0058a0005c0012t0001g0050 | 3 | HG03209.hp2 HG03453.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.282+4828C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665599 | ||||||
chr3:120665771
|
G | A | 46 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(43): Show | 51 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.282+4656C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665771 | ||||||
chr3:120665777
|
A | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0034others(2): Show | 6 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+4650T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665777 | ||||||
chr3:120665816
|
G | C | 1 | a0002c0002t0001g0301 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.282+4611C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665816 | ||||||
chr3:120666019
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0084a0001c0001t0001g0244others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+4408A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666019 | ||||||
chr3:120666181
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.282+4246C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666181 | ||||||
chr3:120666293
|
G | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.282+4134C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666293 | ||||||
chr3:120666395
|
G | A | 2 | a0001c0004t0001g0067a0001c0004t0001g0068 | 2 | HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.282+4032C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666395 | ||||||
chr3:120666409
|
G | A | 61 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0033others(58): Show | 63 | HG00438.hp2 HG00609.hp1 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.282+4018C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666409 | ||||||
chr3:120666624
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.282+3803T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666624 | ||||||
chr3:120666625
|
G | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0066others(12): Show | 17 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.282+3802C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666625 | ||||||
chr3:120666958
|
G | A | 2 | a0001c0004t0001g0067a0001c0004t0001g0068 | 2 | HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.282+3469C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666958 | ||||||
chr3:120667089
|
C | T | 15 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0184others(12): Show | 15 | HG00323.hp1 HG00323.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.282+3338G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667089 | ||||||
chr3:120667098
|
G | A | 15 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0184others(12): Show | 15 | HG00323.hp1 HG00323.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.282+3329C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667098 | ||||||
chr3:120667297
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.282+3130C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667297 | ||||||
chr3:120667326
|
C | CA | 48 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(45): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.282+3100dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667326 | ||||||
chr3:120667326
|
C | CAA | 18 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0045others(15): Show | 21 | HG00741.hp1 HG01243.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.282+3099_282+3100d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667326 | ||||||
chr3:120667326
|
C | CAAA | 6 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0064others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+3098_282+3100d others(5): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667326 | ||||||
chr3:120667326
|
CA | C | 36 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0027others(33): Show | 37 | HG00323.hp1 HG00323.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.282+3100delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667326 | ||||||
chr3:120667326
|
CAA | C | 56 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(53): Show | 59 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.282+3099_282+3100d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667326 | ||||||
chr3:120667443
|
A | G | 4 | a0003c0005t0001g0028a0003c0005t0001g0030a0003c0005t0001g0031others(1): Show | 4 | HG01099.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+2984T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667443 | ||||||
chr3:120667456
|
T | C | 53 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 56 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.282+2971A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667456 | ||||||
chr3:120667591
|
G | A | 53 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 56 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.282+2836C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667591 | ||||||
chr3:120667879
|
A | G | 1 | a0002c0002t0001g0328 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.282+2548T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667879 | ||||||
chr3:120667885
|
A | G | 3 | a0001c0001t0001g0066a0001c0004t0001g0067a0001c0004t0001g0068 | 3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.282+2542T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667885 | ||||||
chr3:120668019
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282+2408A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668019 | ||||||
chr3:120668034
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.282+2393G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668034 | ||||||
chr3:120668288
|
T | G | 4 | a0003c0005t0001g0028a0003c0005t0001g0030a0003c0005t0001g0031others(1): Show | 4 | HG01099.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+2139A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668288 | ||||||
chr3:120668444
|
G | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.282+1983C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668444 | ||||||
chr3:120668486
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282+1941C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668486 | ||||||
chr3:120668531
|
G | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0074others(15): Show | 20 | HG00735.hp1 HG01099.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.282+1896C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668531 | ||||||
chr3:120668673
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.282+1754G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668673 | ||||||
chr3:120668740
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0044others(23): Show | 29 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.282+1687G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668740 | ||||||
chr3:120668759
|
AT | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0033others(12): Show | 16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.282+1667delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668759 | ||||||
chr3:120668812
|
G | C | 56 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(53): Show | 59 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.282+1615C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668812 | ||||||
chr3:120668869
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.282+1558G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668869 | ||||||
chr3:120668910
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.282+1517C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668910 | ||||||
chr3:120668940
|
C | T | 1 | a0002c0007t0001g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.282+1487G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668940 | ||||||
chr3:120668941
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.282+1486C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668941 | ||||||
chr3:120668968
|
CTA | C | 57 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(54): Show | 60 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.282+1457_282+1458d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668968 | ||||||
chr3:120669033
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.282+1394C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669033 | ||||||
chr3:120669048
|
C | T | 3 | a0002c0002t0001g0263a0002c0002t0001g0264a0002c0002t0001g0345 | 3 | HG02071.hp2 HG02135.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.282+1379G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669048 | ||||||
chr3:120669056
|
A | G | 1 | a0003c0005t0001g0029 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.282+1371T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669056 | ||||||
chr3:120669062
|
A | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0033others(10): Show | 14 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.282+1365T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669062 | ||||||
chr3:120669139
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282+1288G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669139 | ||||||
chr3:120669267
|
C | CA | 30 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0042others(27): Show | 33 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.282+1159dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669267 | ||||||
chr3:120669277
|
A | C | 3 | a0001c0001t0001g0066a0001c0004t0001g0067a0001c0004t0001g0068 | 3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.282+1150T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669277 | ||||||
chr3:120669440
|
C | T | 50 | a0002c0002t0001g0019a0002c0002t0001g0069a0002c0002t0001g0181others(47): Show | 51 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.282+987G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669440 | ||||||
chr3:120669441
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.282+986C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669441 | ||||||
chr3:120669447
|
G | GCA | 62 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(59): Show | 69 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.282+978_282+979dup others(2): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | ||||||
chr3:120669447
|
G | GCACA | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0021others(38): Show | 45 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.282+976_282+979dup others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | ||||||
chr3:120669447
|
G | GCACACA | 10 | a0001c0001t0001g0023a0001c0001t0001g0117a0001c0001t0001g0234others(7): Show | 10 | HG00323.hp1 HG00558.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.282+974_282+979dup others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | ||||||
chr3:120669447
|
G | GCACACAC others(1): Show |
7 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0079others(4): Show | 12 | HG01074.hp1 HG01106.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.282+972_282+979dup others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | ||||||
chr3:120669447
|
G | GCGCGCAC others(1): Show |
4 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0341others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+979_282+980ins others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | ||||||
chr3:120669447
|
GCA | G | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0033others(59): Show | 64 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.282+978_282+979del others(2): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | ||||||
chr3:120669447
|
GCACA | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(47): Show | 57 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.282+976_282+979del others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | ||||||
chr3:120669447
|
GCACACA | G | 5 | a0001c0001t0001g0044a0001c0001t0001g0094a0001c0001t0002g0022others(2): Show | 5 | HG01109.hp1 HG01358.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+974_282+979del others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | ||||||
chr3:120669447
|
GCACACAC others(3): Show |
G | 1 | a0001c0001t0001g0074 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.282+970_282+979del others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | ||||||
chr3:120669447
|
GCACACAC others(5): Show |
G | 1 | a0002c0002t0001g0164 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.282+968_282+979del others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | ||||||
chr3:120669449
|
A | G | 1 | a0001c0003t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.282+978T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669449 | ||||||
chr3:120669507
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.282+920C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669507 | ||||||
chr3:120669520
|
C | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.282+907G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669520 | ||||||
chr3:120669576
|
C | G | 1 | a0002c0002t0001g0254 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.282+851G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669576 | ||||||
chr3:120669624
|
A | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(112): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.282+803T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669624 | ||||||
chr3:120669923
|
T | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(112): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.282+504A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669923 | ||||||
chr3:120669925
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.282+502A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669925 | ||||||
chr3:120670034
|
T | A | 1 | a0001c0001t0001g0156 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.282+393A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670034 | ||||||
chr3:120670082
|
C | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0074others(12): Show | 17 | HG01099.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.282+345G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670082 | ||||||
chr3:120670083
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.282+344T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670083 | ||||||
chr3:120670140
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(62): Show | 72 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.282+287G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670140 | ||||||
chr3:120670188
|
G | A | 1 | a0001c0004t0001g0243 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.282+239C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670188 | ||||||
chr3:120670205
|
G | A | 1 | a0002c0002t0001g0250 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.282+222C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670205 | ||||||
chr3:120670250
|
T | C | 4 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG00735.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+177A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670250 | ||||||
chr3:120670369
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.282+58C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670369 | ||||||
chr3:120670375
|
C | G | 1 | a0002c0002t0001g0253 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.282+52G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670375 | ||||||
chr3:120670396
|
T | C | 1 | a0001c0004t0001g0243 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.282+31A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670396 | ||||||
chr3:120670413
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.282+14G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670413 | ||||||
chr3:120670582
|
G | A | 3 | a0001c0001t0001g0066a0001c0004t0001g0067a0001c0004t0001g0068 | 3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.177-50C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670582 | ||||||
chr3:120670584
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.177-52C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670584 | ||||||
chr3:120670644
|
A | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.177-112T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670644 | ||||||
chr3:120670739
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.177-207G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670739 | ||||||
chr3:120670742
|
C | T | 1 | a0002c0002t0001g0252 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.177-210G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670742 | ||||||
chr3:120670804
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0081 | 2 | HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.177-272A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670804 | ||||||
chr3:120670833
|
G | T | 1 | a0002c0002t0001g0246 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.177-301C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670833 | ||||||
chr3:120671071
|
A | G | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0082others(1): Show | 4 | HG02055.hp1 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.177-539T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671071 | ||||||
chr3:120671177
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0074others(7): Show | 12 | HG02132.hp2 HG02257.hp1 HG03195.hp1 others(9): Show |
intron_variant | MODIFIER | c.177-645G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671177 | ||||||
chr3:120671264
|
C | A | 1 | a0001c0001t0001g0163 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.177-732G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671264 | ||||||
chr3:120671460
|
G | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0074others(16): Show | 21 | HG00735.hp1 HG01099.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.177-928C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671460 | ||||||
chr3:120671672
|
T | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(60): Show | 70 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.177-1140A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671672 | ||||||
chr3:120671673
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.177-1141C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671673 | ||||||
chr3:120671701
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.177-1169G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671701 | ||||||
chr3:120671758
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.177-1226G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671758 | ||||||
chr3:120671779
|
C | G | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.177-1247G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671779 | ||||||
chr3:120671907
|
T | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.177-1375A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671907 | ||||||
chr3:120672068
|
A | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.177-1536T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672068 | ||||||
chr3:120672082
|
C | G | 3 | a0001c0001t0001g0071a0001c0001t0002g0022a0001c0003t0001g0070 | 3 | HG01109.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.177-1550G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672082 | ||||||
chr3:120672237
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.177-1705G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672237 | ||||||
chr3:120672343
|
A | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(62): Show | 72 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.177-1811T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672343 | ||||||
chr3:120672358
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.177-1826G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672358 | ||||||
chr3:120672367
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | NA18941.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.177-1835T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672367 | ||||||
chr3:120672439
|
G | A | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0341others(2): Show | 5 | HG02280.hp2 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.177-1907C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672439 | ||||||
chr3:120672570
|
T | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(62): Show | 72 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.177-2038A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672570 | ||||||
chr3:120672756
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | NA18941.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.176+2145G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672756 | ||||||
chr3:120673036
|
A | T | 1 | a0002c0002t0001g0251 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.176+1865T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673036 | ||||||
chr3:120673097
|
T | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(56): Show | 66 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.176+1804A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673097 | ||||||
chr3:120673158
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.176+1743G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673158 | ||||||
chr3:120673165
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.176+1736C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673165 | ||||||
chr3:120673220
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.176+1681G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673220 | ||||||
chr3:120673471
|
A | G | 51 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 54 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.176+1430T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673471 | ||||||
chr3:120673479
|
C | T | 64 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(61): Show | 68 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.176+1422G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673479 | ||||||
chr3:120673496
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.176+1405T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673496 | ||||||
chr3:120673507
|
CAG | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 93 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.176+1392_176+1393d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673507 | ||||||
chr3:120673581
|
C | A | 50 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 53 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.176+1320G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673581 | ||||||
chr3:120673624
|
T | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(62): Show | 72 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.176+1277A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673624 | ||||||
chr3:120673657
|
G | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(62): Show | 72 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.176+1244C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673657 | ||||||
chr3:120673745
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(62): Show | 72 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.176+1156C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673745 | ||||||
chr3:120673876
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.176+1025G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673876 | ||||||
chr3:120674148
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.176+753A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674148 | ||||||
chr3:120674259
|
C | T | 19 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0074others(16): Show | 21 | HG00735.hp1 HG01099.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.176+642G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674259 | ||||||
chr3:120674270
|
C | T | 5 | a0002c0002t0001g0246a0002c0002t0001g0247a0002c0002t0001g0248others(2): Show | 5 | NA18947.hp1 NA19005.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.176+631G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674270 | ||||||
chr3:120674459
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0044others(22): Show | 28 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.176+442C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674459 | ||||||
chr3:120674511
|
T | C | 3 | a0001c0001t0001g0066a0001c0004t0001g0067a0001c0004t0001g0068 | 3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.176+390A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674511 | ||||||
chr3:120674550
|
T | TAAAACAA others(3): Show |
31 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0025others(28): Show | 34 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.176+341_176+350dup others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674550 | ||||||
chr3:120674550
|
T | TAAAACAA others(8): Show |
34 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(31): Show | 38 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.176+336_176+350dup others(15): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674550 | ||||||
chr3:120674787
|
A | C | 3 | a0001c0001t0001g0066a0001c0004t0001g0067a0001c0004t0001g0068 | 3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.176+114T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674787 | ||||||
chr3:120675112
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.88-123C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675112 | ||||||
chr3:120675117
|
G | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | NA18984.hp1 NA18991.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.88-128C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675117 | ||||||
chr3:120675152
|
C | T | 3 | a0001c0001t0001g0071a0001c0001t0002g0022a0001c0003t0001g0070 | 3 | HG01109.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.88-163G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675152 | ||||||
chr3:120675205
|
A | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(232): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.88-216T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675205 | ||||||
chr3:120675239
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(67): Show | 75 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.88-250C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675239 | ||||||
chr3:120675330
|
CT | C | 62 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(59): Show | 66 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.88-342delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675330 | ||||||
chr3:120675447
|
T | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(62): Show | 72 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.87+345A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675447 | ||||||
chr3:120675536
|
T | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.87+256A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675536 | ||||||
chr3:120675542
|
T | G | 1 | a0001c0001t0001g0021 | 2 | NA18983.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.87+250A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675542 | ||||||
chr3:120675579
|
C | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.87+213G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675579 | ||||||
chr3:120675608
|
A | G | 3 | a0002c0002t0001g0181a0002c0002t0001g0182a0002c0002t0001g0183 | 3 | NA18961.hp2 NA19064.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.87+184T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675608 | ||||||
chr3:120675674
|
T | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(62): Show | 72 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.87+118A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675674 | ||||||
chr3:120675757
|
T | A | 51 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 54 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.87+35A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675757 | ||||||
chr3:120676038
|
G | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.16-175C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676038 | ||||||
chr3:120676441
|
AG | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.16-579delC | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676441 | ||||||
chr3:120676453
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.16-590C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676453 | ||||||
chr3:120676609
|
G | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(41): Show | 49 | HG00735.hp1 HG01099.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.16-746C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676609 | ||||||
chr3:120676771
|
A | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.16-908T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676771 | ||||||
chr3:120676775
|
G | A | 3 | a0001c0001t0001g0066a0001c0004t0001g0067a0001c0004t0001g0068 | 3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.16-912C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676775 | ||||||
chr3:120676905
|
C | T | 51 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 54 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.16-1042G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676905 | ||||||
chr3:120677019
|
A | G | 33 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(30): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.16-1156T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677019 | ||||||
chr3:120677279
|
A | G | 40 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(37): Show | 44 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.16-1416T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677279 | ||||||
chr3:120677292
|
C | G | 1 | a0001c0001t0001g0092 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.16-1429G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677292 | ||||||
chr3:120677379
|
G | A | 4 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0337others(1): Show | 4 | HG00323.hp1 HG02293.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-1516C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677379 | ||||||
chr3:120677414
|
C | G | 3 | a0001c0001t0001g0066a0001c0004t0001g0067a0001c0004t0001g0068 | 3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.16-1551G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677414 | ||||||
chr3:120677422
|
G | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0072 | 3 | HG02055.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.16-1559C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677422 | ||||||
chr3:120677442
|
A | G | 2 | a0002c0002t0001g0179a0002c0002t0001g0180 | 2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.16-1579T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677442 | ||||||
chr3:120677478
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.16-1615C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677478 | ||||||
chr3:120677481
|
C | T | 3 | a0001c0001t0001g0066a0001c0004t0001g0067a0001c0004t0001g0068 | 3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.16-1618G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677481 | ||||||
chr3:120677619
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.16-1756G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677619 | ||||||
chr3:120677627
|
T | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 96 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.16-1764A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677627 | ||||||
chr3:120677756
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0033others(10): Show | 14 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.16-1893G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677756 | ||||||
chr3:120677793
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.16-1930G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677793 | ||||||
chr3:120677852
|
C | A | 2 | a0002c0002t0001g0339a0002c0002t0001g0340 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.16-1989G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677852 | ||||||
chr3:120677889
|
T | C | 2 | a0001c0001t0001g0341a0001c0001t0001g0342 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.16-2026A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677889 | ||||||
chr3:120677959
|
G | A | 1 | a0002c0002t0001g0343 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.16-2096C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677959 | ||||||
chr3:120678021
|
T | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0074others(12): Show | 17 | HG01099.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-2158A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678021 | ||||||
chr3:120678128
|
A | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(105): Show | 117 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(114): Show |
intron_variant | MODIFIER | c.16-2265T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678128 | ||||||
chr3:120678246
|
A | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 96 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.16-2383T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678246 | ||||||
chr3:120678248
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.16-2385C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678248 | ||||||
chr3:120678249
|
C | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0074others(12): Show | 17 | HG01099.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-2386G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678249 | ||||||
chr3:120678526
|
G | A | 1 | a0001c0001t0001g0344 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.16-2663C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678526 | ||||||
chr3:120678666
|
G | C | 1 | a0001c0001t0001g0065 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.16-2803C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678666 | ||||||
chr3:120678699
|
A | G | 1 | a0001c0003t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.16-2836T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678699 | ||||||
chr3:120678769
|
CAG | C | 4 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG00735.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-2908_16-2907del others(2): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678769 | ||||||
chr3:120678806
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.16-2943G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678806 | ||||||
chr3:120678837
|
A | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0072 | 3 | HG02055.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.16-2974T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678837 | ||||||
chr3:120678868
|
CA | C | 3 | a0001c0001t0001g0071a0001c0001t0002g0022a0001c0003t0001g0070 | 3 | HG01109.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.16-3006delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678868 | ||||||
chr3:120678903
|
C | T | 51 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 54 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.16-3040G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678903 | ||||||
chr3:120678904
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.16-3041C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678904 | ||||||
chr3:120678922
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 101 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.16-3059A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678922 | ||||||
chr3:120679003
|
G | T | 3 | a0001c0001t0001g0071a0001c0001t0002g0022a0001c0003t0001g0070 | 3 | HG01109.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.15+3094C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679003 | ||||||
chr3:120679012
|
C | T | 1 | a0002c0002t0001g0176 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.15+3085G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679012 | ||||||
chr3:120679118
|
G | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG02683.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.15+2979C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679118 | ||||||
chr3:120679135
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.15+2962A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679135 | ||||||
chr3:120679219
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.15+2878C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679219 | ||||||
chr3:120679247
|
G | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0074others(7): Show | 12 | HG02132.hp2 HG02257.hp1 HG03195.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+2850C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679247 | ||||||
chr3:120679275
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.15+2822G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679275 | ||||||
chr3:120679447
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.15+2650C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679447 | ||||||
chr3:120679523
|
T | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.15+2574A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679523 | ||||||
chr3:120679651
|
T | A | 1 | a0002c0002t0001g0345 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.15+2446A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679651 | ||||||
chr3:120679698
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.15+2399G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679698 | ||||||
chr3:120679724
|
C | T | 4 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG00735.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+2373G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679724 | ||||||
chr3:120679757
|
G | T | 1 | a0001c0001t0001g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.15+2340C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679757 | ||||||
chr3:120679837
|
C | T | 10 | a0002c0002t0001g0164a0002c0002t0001g0165a0002c0002t0001g0166others(7): Show | 10 | HG00597.hp1 HG00609.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+2260G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679837 | ||||||
chr3:120679850
|
G | C | 1 | a0001c0001t0001g0346 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.15+2247C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679850 | ||||||
chr3:120679970
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 101 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.15+2127T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679970 | ||||||
chr3:120679975
|
G | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0074others(11): Show | 16 | HG00735.hp1 HG02132.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+2122C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679975 | ||||||
chr3:120680106
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.15+1991C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120680106 | ||||||
chr3:120680322
|
A | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.15+1775T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120680322 | ||||||
chr3:120680512
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.15+1585C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120680512 | ||||||
chr3:120680728
|
C | A | 1 | a0002c0002t0001g0347 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.15+1369G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120680728 | ||||||
chr3:120680858
|
CCAGTTCC others(18): Show |
C | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG00735.hp1 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.15+1214_15+1238del others(25): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120680858 | ||||||
chr3:120681015
|
A | C | 4 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | HG02258.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+1082T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681015 | ||||||
chr3:120681070
|
T | G | 4 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG00735.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+1027A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681070 | ||||||
chr3:120681268
|
T | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(30): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.15+829A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681268 | ||||||
chr3:120681287
|
G | A | 51 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 54 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.15+810C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681287 | ||||||
chr3:120681568
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.15+529G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681568 | ||||||
chr3:120681628
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.15+469T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681628 | ||||||
chr3:120681636
|
G | A | 1 | a0001c0001t0001g0348 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.15+461C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681636 | ||||||
chr3:120681811
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.15+286G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681811 |