geneid | 374569 |
---|---|
ensemblid | ENSG00000166183.16 |
hgncid | 20123 |
symbol | ASPG |
name | asparaginase |
refseq_nuc | NM_001080464.3 |
refseq_prot | NP_001073933.2 |
ensembl_nuc | ENST00000551177.6 |
ensembl_prot | ENSP00000450040.1 |
mane_status | MANE Select |
chr | chr14 |
start | 104085700 |
end | 104115582 |
strand | + |
ver | v1.2 |
region | chr14:104085700-104115582 |
region5000 | chr14:104080700-104120582 |
regionname0 | ASPG_chr14_104085700_104115582 |
regionname5000 | ASPG_chr14_104080700_104120582 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 573 | 153 | 25 | 45 | 51 | 11 | 20 | 34 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002 | 0/1 | 573 | 153 | 54 | 25 | 53 | 1 | 19 | 41 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0003 | 0/0 | 573 | 51 | 8 | 8 | 27 | 4 | 4 | 14 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0004 | 0/0 | 573 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0005 | 0/0 | 573 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0006 | 0/0 | 573 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0007 | 0/0 | 573 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0008 | 0/0 | 573 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0009 | 0/0 | 573 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0010 | 0/0 | 573 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0011 | 0/0 | 573 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0012 | 0/0 | 573 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1722 | 138 | 16 | 43 | 49 | 10 | 19 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0002 | 0/1 | 1722 | 85 | 12 | 15 | 45 | 0 | 12 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0003 | 0/0 | 1722 | 57 | 31 | 10 | 8 | 1 | 7 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0004 | 0/0 | 1722 | 48 | 5 | 8 | 27 | 4 | 4 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0005 | 0/0 | 1722 | 6 | 6 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0006 | 0/0 | 1722 | 5 | 2 | 1 | 1 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0007 | 0/0 | 1722 | 5 | 5 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0008 | 0/0 | 1722 | 3 | 2 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0009 | 0/0 | 1722 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0010 | 0/0 | 1722 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0011 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0012 | 0/0 | 1722 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0013 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0014 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0015 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0016 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0017 | 0/0 | 1722 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0018 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0019 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0020 | 0/0 | 1722 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0021 | 0/0 | 1722 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0022 | 0/0 | 1722 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0023 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0024 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0025 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0026 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
c0027 | 0/0 | 1722 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3110 | 109 | 2 | 33 | 47 | 11 | 16 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0002 | 0/0 | 3110 | 90 | 21 | 17 | 39 | 0 | 13 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0003 | 0/0 | 3110 | 46 | 6 | 9 | 23 | 3 | 5 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0004 | 0/0 | 3110 | 21 | 7 | 10 | 0 | 0 | 4 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0005 | 1/0 | 3110 | 15 | 11 | 3 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0006 | 0/0 | 3110 | 11 | 9 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0007 | 0/0 | 3110 | 8 | 3 | 0 | 5 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0008 | 0/0 | 3110 | 8 | 8 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0009 | 0/0 | 3110 | 6 | 0 | 2 | 0 | 1 | 3 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0010 | 0/0 | 3110 | 4 | 4 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0011 | 0/0 | 3110 | 3 | 3 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0012 | 0/0 | 3110 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0013 | 0/0 | 3110 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0014 | 0/0 | 3110 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0015 | 0/0 | 3110 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0016 | 0/0 | 3110 | 3 | 2 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0017 | 0/0 | 3110 | 3 | 3 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0018 | 0/0 | 3110 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0019 | 0/1 | 3110 | 2 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0020 | 0/0 | 3110 | 2 | 0 | 0 | 1 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0021 | 0/0 | 3110 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0022 | 0/0 | 3110 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0023 | 0/0 | 3110 | 2 | 1 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0024 | 0/0 | 3110 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0025 | 0/0 | 3110 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0026 | 0/0 | 3110 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0027 | 0/0 | 3110 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0028 | 0/0 | 3110 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0029 | 0/0 | 3110 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0030 | 0/0 | 3110 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0031 | 0/0 | 3110 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0032 | 0/0 | 3110 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0033 | 0/0 | 3110 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0034 | 0/0 | 3110 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0035 | 0/0 | 3110 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0036 | 0/0 | 3110 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0037 | 0/0 | 3110 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0038 | 0/0 | 3110 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
t0039 | 0/0 | 3110 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 17 | 0 | 4 | 9 | 1 | 3 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0002 | 0/0 | 11 | 0 | 8 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0003 | 0/0 | 9 | 0 | 0 | 8 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0005 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0006 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0007 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1722 | 138 | 16 | 43 | 49 | 10 | 19 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0006 | 0/0 | 1722 | 5 | 2 | 1 | 1 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0007 | 0/0 | 1722 | 5 | 5 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0018 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0019 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0022 | 0/0 | 1722 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0024 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0027 | 0/0 | 1722 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0002 | 0/1 | 1722 | 85 | 12 | 15 | 45 | 0 | 12 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003 | 0/0 | 1722 | 57 | 31 | 10 | 8 | 1 | 7 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0005 | 0/0 | 1722 | 6 | 6 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0010 | 0/0 | 1722 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0013 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0016 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0026 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0003c0004 | 0/0 | 1722 | 48 | 5 | 8 | 27 | 4 | 4 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0003c0009 | 0/0 | 1722 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0003c0025 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0004c0008 | 0/0 | 1722 | 3 | 2 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0005c0021 | 0/0 | 1722 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0006c0020 | 0/0 | 1722 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0007c0023 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0008c0017 | 0/0 | 1722 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0009c0014 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0010c0015 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0011c0011 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0012c0012 | 0/0 | 1722 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4831 | 91 | 2 | 28 | 38 | 10 | 13 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0002 | 0/0 | 4831 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0004 | 0/0 | 4831 | 18 | 5 | 9 | 0 | 0 | 4 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0005 | 1/0 | 4831 | 5 | 2 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0007 | 0/0 | 4831 | 7 | 3 | 0 | 4 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0010 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0011 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0014 | 0/0 | 4831 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0020 | 0/0 | 4831 | 2 | 0 | 0 | 1 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0024 | 0/0 | 4831 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0025 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0031 | 0/0 | 4831 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0032 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0033 | 0/0 | 4831 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0034 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0035 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0001t0036 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0006t0002 | 0/0 | 4831 | 4 | 2 | 1 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0006t0028 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0007t0002 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0007t0008 | 0/0 | 4831 | 4 | 4 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0018t0001 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0019t0010 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0022t0001 | 0/0 | 4831 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0024t0011 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0001c0027t0001 | 0/0 | 4831 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0002t0002 | 0/0 | 4831 | 71 | 6 | 15 | 39 | 0 | 11 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0002t0005 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0002t0008 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0002t0013 | 0/0 | 4831 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0002t0015 | 0/0 | 4831 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0002t0019 | 0/1 | 4831 | 2 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0002t0022 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0002t0027 | 0/0 | 4831 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0001 | 0/0 | 4831 | 14 | 0 | 4 | 7 | 0 | 3 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0002 | 0/0 | 4831 | 6 | 5 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0005 | 0/0 | 4831 | 7 | 6 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0006 | 0/0 | 4831 | 9 | 7 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0007 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0009 | 0/0 | 4831 | 6 | 0 | 2 | 0 | 1 | 3 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0010 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0011 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0016 | 0/0 | 4831 | 3 | 2 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0017 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0018 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0021 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0037 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0003t0038 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0005t0002 | 0/0 | 4831 | 4 | 4 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0005t0008 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0010t0002 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0013t0039 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0016t0006 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0002c0026t0006 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0003c0004t0003 | 0/0 | 4831 | 43 | 5 | 8 | 23 | 3 | 4 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0003c0004t0012 | 0/0 | 4831 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0003c0004t0026 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0003c0004t0030 | 0/0 | 4831 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0003c0009t0005 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0003c0025t0003 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0004c0008t0004 | 0/0 | 4831 | 3 | 2 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0005c0021t0003 | 0/0 | 4831 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0006c0020t0029 | 0/0 | 4831 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0007c0023t0001 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0008c0017t0003 | 0/0 | 4831 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0009c0014t0017 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0010c0015t0002 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0011c0011t0023 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
a0012c0012t0023 | 0/0 | 4831 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | copy fasta | chr14 | 104080700 | 104120582 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 13 | 0 | 4 | 5 | 1 | 3 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0005g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0005g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0007g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0011g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0014g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0020g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0020g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0024g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0025g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0031g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0032g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0033g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0035g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0036g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0006t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0006t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0006t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0006t0028g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0007t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0007t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0007t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0007t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0007t0008g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0018t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0019t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0022t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0024t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0027t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0002 | 0/0 | 11 | 0 | 8 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0006 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0008g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0013g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0013g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0013g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0015g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0015g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0019g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0019g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0022g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0027g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0005g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0005g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0006g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0006g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0006g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0006g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0007g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0009g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0009g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0009g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0009g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0009g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0011g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0016g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0016g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0016g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0017g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0017g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0018g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0018g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0021g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0021g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0037g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0038g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0005t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0005t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0005t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0005t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0005t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0010t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0013t0039g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0016t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0026t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0007 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0012g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0026g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0030g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0009t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0009t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0025t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0004c0008t0004g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0005c0021t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0006c0020t0029g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0007c0023t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0008c0017t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0009c0014t0017g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0010c0015t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0011c0011t0023g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0012c0012t0023g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | GBR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00140 | hp2 | a0001 | c0027 | t0001 | g0136 | EUR | GBR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00280 | hp2 | a0002 | c0003 | t0009 | g0182 | EUR | FIN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00438 | hp1 | a0003 | c0004 | t0026 | g0030 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00438 | hp2 | a0001 | c0001 | t0007 | g0017 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00558 | hp1 | a0001 | c0001 | t0034 | g0001 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00597 | hp1 | a0003 | c0004 | t0003 | g0251 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00597 | hp2 | a0003 | c0004 | t0003 | g0072 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00609 | hp1 | a0003 | c0004 | t0003 | g0093 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00639 | hp1 | a0004 | c0008 | t0004 | g0021 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00642 | hp2 | a0002 | c0003 | t0009 | g0183 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00673 | hp2 | a0001 | c0006 | t0028 | g0143 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00733 | hp1 | a0002 | c0003 | t0005 | g0056 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00735 | hp1 | a0002 | c0003 | t0006 | g0240 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00735 | hp2 | a0001 | c0022 | t0001 | g0068 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00741 | hp2 | a0003 | c0004 | t0003 | g0074 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01070 | hp1 | a0003 | c0004 | t0003 | g0007 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01074 | hp1 | a0002 | c0003 | t0016 | g0167 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01074 | hp2 | a0002 | c0003 | t0001 | g0019 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01081 | hp2 | a0003 | c0004 | t0003 | g0096 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01099 | hp2 | a0002 | c0003 | t0006 | g0051 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01106 | hp1 | a0003 | c0004 | t0003 | g0097 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01109 | hp1 | a0003 | c0004 | t0003 | g0007 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01167 | hp1 | a0002 | c0003 | t0001 | g0019 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01168 | hp1 | a0012 | c0012 | t0023 | g0237 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01243 | hp1 | a0003 | c0004 | t0003 | g0075 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01256 | hp2 | a0001 | c0001 | t0024 | g0037 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01257 | hp2 | a0003 | c0004 | t0003 | g0029 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01258 | hp1 | a0001 | c0001 | t0024 | g0037 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01258 | hp2 | a0003 | c0004 | t0003 | g0029 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0250 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01346 | hp1 | a0001 | c0001 | t0031 | g0148 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01433 | hp2 | a0001 | c0006 | t0002 | g0126 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01496 | hp1 | a0002 | c0003 | t0009 | g0179 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01515 | hp1 | a0003 | c0004 | t0003 | g0026 | EUR | IBS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01517 | hp2 | a0003 | c0004 | t0003 | g0026 | EUR | IBS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01884 | hp1 | a0004 | c0008 | t0004 | g0021 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01884 | hp2 | a0002 | c0003 | t0005 | g0057 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01891 | hp2 | a0002 | c0003 | t0005 | g0055 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0202 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0203 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01978 | hp1 | a0002 | c0003 | t0001 | g0044 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02015 | hp2 | a0001 | c0018 | t0001 | g0034 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02027 | hp2 | a0001 | c0001 | t0007 | g0118 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02055 | hp1 | a0002 | c0003 | t0006 | g0239 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02055 | hp2 | a0002 | c0003 | t0018 | g0177 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02071 | hp2 | a0002 | c0003 | t0001 | g0019 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02074 | hp2 | a0003 | c0004 | t0003 | g0012 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02080 | hp1 | a0003 | c0004 | t0003 | g0073 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02083 | hp1 | a0003 | c0004 | t0003 | g0092 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02129 | hp1 | a0002 | c0003 | t0001 | g0044 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02132 | hp1 | a0002 | c0002 | t0013 | g0197 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02135 | hp1 | a0003 | c0004 | t0003 | g0094 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02145 | hp1 | a0002 | c0003 | t0010 | g0238 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02145 | hp2 | a0003 | c0025 | t0003 | g0084 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02155 | hp1 | a0003 | c0004 | t0003 | g0089 | EAS | CDX | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02165 | hp2 | a0001 | c0001 | t0036 | g0015 | EAS | CDX | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02257 | hp1 | a0001 | c0001 | t0035 | g0133 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02258 | hp1 | a0003 | c0004 | t0003 | g0104 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02258 | hp2 | a0002 | c0026 | t0006 | g0220 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02273 | hp1 | a0006 | c0020 | t0029 | g0052 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02280 | hp1 | a0002 | c0003 | t0006 | g0241 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02280 | hp2 | a0002 | c0010 | t0002 | g0046 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02300 | hp1 | a0002 | c0003 | t0001 | g0234 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0172 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02451 | hp2 | a0001 | c0019 | t0010 | g0245 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02523 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02572 | hp1 | a0002 | c0003 | t0010 | g0159 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02572 | hp2 | a0002 | c0003 | t0002 | g0178 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0242 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02615 | hp2 | a0001 | c0007 | t0002 | g0248 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02622 | hp1 | a0002 | c0003 | t0017 | g0162 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02622 | hp2 | a0002 | c0003 | t0005 | g0058 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0061 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02630 | hp2 | a0001 | c0024 | t0011 | g0060 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02647 | hp1 | a0001 | c0001 | t0025 | g0243 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0173 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02698 | hp1 | a0002 | c0003 | t0009 | g0227 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02698 | hp2 | a0005 | c0021 | t0003 | g0063 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02717 | hp1 | a0002 | c0003 | t0017 | g0171 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02717 | hp2 | a0002 | c0003 | t0018 | g0181 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0244 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0218 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02735 | hp1 | a0002 | c0003 | t0009 | g0042 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02738 | hp1 | a0002 | c0003 | t0001 | g0211 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0209 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02809 | hp1 | a0002 | c0005 | t0002 | g0175 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02809 | hp2 | a0002 | c0013 | t0039 | g0168 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02818 | hp1 | a0011 | c0011 | t0023 | g0154 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02818 | hp2 | a0001 | c0006 | t0002 | g0033 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02886 | hp1 | a0002 | c0003 | t0006 | g0050 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0047 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02895 | hp1 | a0003 | c0004 | t0003 | g0095 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02895 | hp2 | a0002 | c0003 | t0002 | g0010 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02896 | hp1 | a0002 | c0003 | t0002 | g0010 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02897 | hp2 | a0010 | c0015 | t0002 | g0235 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02965 | hp1 | a0002 | c0003 | t0006 | g0049 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02965 | hp2 | a0002 | c0010 | t0002 | g0046 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02970 | hp1 | a0002 | c0016 | t0006 | g0212 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02970 | hp2 | a0002 | c0005 | t0002 | g0041 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02976 | hp1 | a0002 | c0003 | t0006 | g0050 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02976 | hp2 | a0001 | c0007 | t0008 | g0247 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03017 | hp1 | a0001 | c0001 | t0020 | g0005 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03041 | hp1 | a0002 | c0003 | t0006 | g0051 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03041 | hp2 | a0002 | c0005 | t0008 | g0228 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03098 | hp1 | a0003 | c0009 | t0005 | g0077 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03098 | hp2 | a0001 | c0001 | t0010 | g0246 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03130 | hp1 | a0002 | c0002 | t0019 | g0174 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03130 | hp2 | a0002 | c0003 | t0011 | g0166 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03139 | hp1 | a0002 | c0003 | t0016 | g0170 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03209 | hp1 | a0002 | c0003 | t0037 | g0169 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03209 | hp2 | a0001 | c0001 | t0007 | g0078 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03225 | hp1 | a0002 | c0005 | t0008 | g0213 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03453 | hp1 | a0001 | c0007 | t0008 | g0080 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03453 | hp2 | a0002 | c0003 | t0002 | g0010 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03486 | hp1 | a0002 | c0002 | t0008 | g0043 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03486 | hp2 | a0002 | c0003 | t0021 | g0180 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03492 | hp2 | a0002 | c0003 | t0009 | g0042 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03516 | hp1 | a0004 | c0008 | t0004 | g0021 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03516 | hp2 | a0002 | c0003 | t0005 | g0184 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03540 | hp2 | a0002 | c0003 | t0016 | g0163 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03669 | hp1 | a0002 | c0003 | t0002 | g0207 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03669 | hp2 | a0003 | c0004 | t0003 | g0030 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03704 | hp2 | a0001 | c0001 | t0033 | g0134 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0205 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0195 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0090 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0225 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03927 | hp1 | a0003 | c0004 | t0003 | g0091 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0048 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03942 | hp1 | a0003 | c0004 | t0003 | g0100 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0048 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0221 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04184 | hp2 | a0002 | c0002 | t0027 | g0204 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0217 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0215 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04204 | hp2 | a0003 | c0004 | t0003 | g0007 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0208 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04228 | hp2 | a0001 | c0006 | t0002 | g0125 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18522 | hp1 | a0001 | c0006 | t0002 | g0033 | AFR | YRI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18522 | hp2 | a0002 | c0002 | t0005 | g0176 | AFR | YRI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18612 | hp2 | a0003 | c0004 | t0003 | g0155 | EAS | CHB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18747 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | CHB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18747 | hp2 | a0003 | c0004 | t0003 | g0064 | EAS | CHB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18906 | hp1 | a0001 | c0007 | t0008 | g0079 | AFR | YRI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18906 | hp2 | a0002 | c0003 | t0005 | g0022 | AFR | YRI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18941 | hp2 | a0001 | c0001 | t0014 | g0001 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18943 | hp1 | a0002 | c0003 | t0001 | g0054 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18944 | hp1 | a0002 | c0002 | t0015 | g0040 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18949 | hp1 | a0002 | c0002 | t0013 | g0188 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18950 | hp1 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18951 | hp2 | a0003 | c0004 | t0003 | g0107 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18952 | hp2 | a0002 | c0002 | t0015 | g0160 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18953 | hp1 | a0002 | c0003 | t0001 | g0196 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18954 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18964 | hp2 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18966 | hp2 | a0002 | c0002 | t0015 | g0040 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18971 | hp1 | a0003 | c0004 | t0012 | g0011 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18971 | hp2 | a0002 | c0003 | t0007 | g0236 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18972 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18977 | hp2 | a0001 | c0001 | t0007 | g0252 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18979 | hp2 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18985 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18985 | hp2 | a0001 | c0001 | t0014 | g0035 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18993 | hp2 | a0003 | c0004 | t0012 | g0011 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18995 | hp1 | a0003 | c0004 | t0003 | g0012 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18997 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19003 | hp1 | a0002 | c0002 | t0013 | g0198 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19003 | hp2 | a0003 | c0004 | t0003 | g0076 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19004 | hp1 | a0007 | c0023 | t0001 | g0109 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19005 | hp1 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19005 | hp2 | a0003 | c0004 | t0012 | g0011 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19012 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19030 | hp1 | a0003 | c0004 | t0003 | g0102 | AFR | LWK | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19030 | hp2 | a0002 | c0002 | t0022 | g0038 | AFR | LWK | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19043 | hp1 | a0002 | c0002 | t0022 | g0038 | AFR | LWK | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19043 | hp2 | a0002 | c0003 | t0021 | g0185 | AFR | LWK | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19060 | hp1 | a0001 | c0001 | t0014 | g0035 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19065 | hp2 | a0003 | c0004 | t0003 | g0088 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19066 | hp2 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19080 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19083 | hp2 | a0001 | c0001 | t0032 | g0112 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19085 | hp1 | a0003 | c0004 | t0003 | g0012 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19085 | hp2 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19089 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19240 | hp1 | a0003 | c0004 | t0003 | g0103 | AFR | YRI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19240 | hp2 | a0002 | c0003 | t0005 | g0022 | AFR | YRI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20129 | hp1 | a0002 | c0005 | t0002 | g0041 | AFR | ASW | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20129 | hp2 | a0002 | c0003 | t0038 | g0165 | AFR | ASW | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20752 | hp1 | a0003 | c0004 | t0003 | g0007 | EUR | TSI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20752 | hp2 | a0003 | c0004 | t0030 | g0003 | EUR | TSI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | TSI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20905 | hp1 | a0002 | c0003 | t0001 | g0210 | SAS | GIH | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20905 | hp2 | a0002 | c0003 | t0001 | g0216 | SAS | GIH | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01123 | hp2 | a0008 | c0017 | t0003 | g0229 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02109 | hp1 | a0002 | c0005 | t0002 | g0223 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02109 | hp2 | a0009 | c0014 | t0017 | g0164 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02486 | hp1 | a0003 | c0009 | t0005 | g0099 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02486 | hp2 | a0003 | c0004 | t0003 | g0098 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02559 | hp1 | a0002 | c0003 | t0006 | g0049 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03471 | hp1 | a0002 | c0002 | t0008 | g0043 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03471 | hp2 | a0002 | c0003 | t0002 | g0010 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG06807 | hp1 | a0002 | c0002 | t0002 | g0222 | AFR | USA | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | USA | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | USA | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20300 | hp2 | a0001 | c0007 | t0008 | g0067 | AFR | USA | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0019 | g0230 | REF | REF | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0059 | REF | REF | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104093496
|
C | A | 2 | a0011a0012 | 2 | HG01168.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.197C>A | p.Ala66Asp | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/16 | 268/4831 | 197/1722 | 66/573 | chr14 | 104093496 | ||
chr14:104093582
|
T | C | 6 | a0002a0008a0009others(3): Show | 158 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(155): Show |
missense_variant | MODERATE | c.283T>C | p.Cys95Arg | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/16 | 354/4831 | 283/1722 | 95/573 | chr14 | 104093582 | ||
chr14:104093585
|
C | G | 6 | a0002a0008a0009others(3): Show | 158 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(155): Show |
missense_variant | MODERATE | c.286C>G | p.Leu96Val | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/16 | 357/4831 | 286/1722 | 96/573 | chr14 | 104093585 | ||
chr14:104103668
|
C | T | 1 | a0007 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.746C>T | p.Ala249Val | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/16 | 817/4831 | 746/1722 | 249/573 | chr14 | 104103668 | ||
chr14:104104476
|
C | A | 1 | a0004 | 3 | HG00639.hp1 HG01884.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.926C>A | p.Ala309Glu | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 8/16 | 997/4831 | 926/1722 | 309/573 | chr14 | 104104476 | ||
chr14:104104717
|
C | G | 3 | a0003a0005a0008 | 53 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(50): Show |
missense_variant | MODERATE | c.1032C>G | p.Ser344Arg | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 9/16 | 1103/4831 | 1032/1722 | 344/573 | chr14 | 104104717 | ||
chr14:104106827
|
T | C | 1 | a0009 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1202T>C | p.Val401Ala | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 11/16 | 1273/4831 | 1202/1722 | 401/573 | chr14 | 104106827 | ||
chr14:104106865
|
G | A | 1 | a0005 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.1240G>A | p.Val414Met | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 11/16 | 1311/4831 | 1240/1722 | 414/573 | chr14 | 104106865 | ||
chr14:104107270
|
T | C | 1 | a0006 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.1358T>C | p.Leu453Pro | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/16 | 1429/4831 | 1358/1722 | 453/573 | chr14 | 104107270 | ||
chr14:104109266
|
G | C | 1 | a0010 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.1471G>C | p.Ala491Pro | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/16 | 1542/4831 | 1471/1722 | 491/573 | chr14 | 104109266 | ||
chr14:104109269
|
T | C | 1 | a0010 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.1474T>C | p.Ser492Pro | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/16 | 1545/4831 | 1474/1722 | 492/573 | chr14 | 104109269 | ||
chr14:104111978
|
T | A | 1 | a0011 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1679T>A | p.Val560Asp | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 15/16 | 1750/4831 | 1679/1722 | 560/573 | chr14 | 104111978 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104085812
|
C | G | 1 | a0001c0027 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.42C>G | p.Val14Val | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/16 | 113/4831 | 42/1722 | 14/573 | chr14 | 104085812 | ||
chr14:104085818
|
C | T | 2 | a0002c0010a0002c0026 | 3 | HG02258.hp2 HG02280.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.48C>T | p.Thr16Thr | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/16 | 119/4831 | 48/1722 | 16/573 | chr14 | 104085818 | ||
chr14:104093515
|
T | C | 12 | a0002c0002a0002c0003a0002c0005others(9): Show | 158 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(155): Show |
synonymous_variant | LOW | c.216T>C | p.Ile72Ile | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/16 | 287/4831 | 216/1722 | 72/573 | chr14 | 104093515 | ||
chr14:104095551
|
C | T | 1 | a0001c0007 | 5 | HG02615.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
synonymous_variant | LOW | c.324C>T | p.His108His | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/16 | 395/4831 | 324/1722 | 108/573 | chr14 | 104095551 | ||
chr14:104095599
|
G | C | 1 | a0003c0009 | 2 | HG02486.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.372G>C | p.Ser124Ser | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/16 | 443/4831 | 372/1722 | 124/573 | chr14 | 104095599 | ||
chr14:104097595
|
G | T | 8 | a0001c0006a0001c0007a0002c0002others(5): Show | 106 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(103): Show |
synonymous_variant | LOW | c.471G>T | p.Leu157Leu | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/16 | 542/4831 | 471/1722 | 157/573 | chr14 | 104097595 | ||
chr14:104098909
|
C | T | 1 | a0001c0024 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.570C>T | p.Asp190Asp | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/16 | 641/4831 | 570/1722 | 190/573 | chr14 | 104098909 | ||
chr14:104103591
|
C | T | 1 | a0002c0005 | 6 | HG02109.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.669C>T | p.Asp223Asp | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/16 | 740/4831 | 669/1722 | 223/573 | chr14 | 104103591 | ||
chr14:104103597
|
G | A | 1 | a0001c0018 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.675G>A | p.Lys225Lys | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/16 | 746/4831 | 675/1722 | 225/573 | chr14 | 104103597 | ||
chr14:104104396
|
G | A | 2 | a0001c0019a0002c0013 | 2 | HG02451.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.846G>A | p.Glu282Glu | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 8/16 | 917/4831 | 846/1722 | 282/573 | chr14 | 104104396 | ||
chr14:104104429
|
C | T | 1 | a0001c0022 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.879C>T | p.Ile293Ile | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 8/16 | 950/4831 | 879/1722 | 293/573 | chr14 | 104104429 | ||
chr14:104109253
|
G | C | 1 | a0002c0016 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.1458G>C | p.Leu486Leu | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/16 | 1529/4831 | 1458/1722 | 486/573 | chr14 | 104109253 | ||
chr14:104109268
|
C | T | 1 | a0010c0015 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.1473C>T | p.Ala491Ala | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/16 | 1544/4831 | 1473/1722 | 491/573 | chr14 | 104109268 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104085711
|
C | G | 6 | a0002c0003t0016a0002c0003t0017a0002c0003t0037others(3): Show | 9 | HG01074.hp1 HG02109.hp2 HG02622.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-60C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/16 | 60 | chr14 | 104085711 | |||||
chr14:104112721
|
C | T | 1 | a0001c0001t0036 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*177C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 177 | chr14 | 104112721 | |||||
chr14:104112752
|
C | T | 1 | a0001c0001t0024 | 2 | HG01256.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*208C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 208 | chr14 | 104112752 | |||||
chr14:104112810
|
T | G | 1 | a0002c0003t0037 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266T>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 266 | chr14 | 104112810 | |||||
chr14:104112873
|
C | G | 57 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(54): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*329C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 329 | chr14 | 104112873 | |||||
chr14:104112877
|
A | G | 5 | a0001c0001t0010a0001c0019t0010a0002c0003t0010others(2): Show | 6 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*333A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 333 | chr14 | 104112877 | |||||
chr14:104112907
|
A | C | 64 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(61): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
3_prime_UTR_variant | MODIFIER | c.*363A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 363 | chr14 | 104112907 | |||||
chr14:104112951
|
C | A | 1 | a0002c0003t0018 | 2 | HG02055.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*407C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 407 | chr14 | 104112951 | |||||
chr14:104113127
|
C | T | 1 | a0001c0001t0025 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*583C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 583 | chr14 | 104113127 | |||||
chr14:104113273
|
T | A | 1 | a0003c0004t0012 | 3 | NA18971.hp1 NA18993.hp2 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*729T>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 729 | chr14 | 104113273 | |||||
chr14:104113279
|
G | A | 6 | a0003c0004t0003a0003c0004t0012a0003c0004t0026others(3): Show | 50 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*735G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 735 | chr14 | 104113279 | |||||
chr14:104113451
|
C | T | 1 | a0001c0001t0035 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*907C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 907 | chr14 | 104113451 | |||||
chr14:104113493
|
C | T | 1 | a0002c0002t0015 | 3 | NA18944.hp1 NA18952.hp2 NA18966.hp2 |
3_prime_UTR_variant | MODIFIER | c.*949C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 949 | chr14 | 104113493 | |||||
chr14:104113695
|
G | C | 1 | a0002c0003t0009 | 6 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1151G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 1151 | chr14 | 104113695 | |||||
chr14:104113818
|
C | T | 2 | a0011c0011t0023a0012c0012t0023 | 2 | HG01168.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1274C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 1274 | chr14 | 104113818 | |||||
chr14:104114049
|
C | T | 1 | a0002c0002t0022 | 2 | NA19030.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1505C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 1505 | chr14 | 104114049 | |||||
chr14:104114057
|
C | T | 17 | a0001c0001t0001a0001c0001t0014a0001c0001t0020others(14): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1513C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 1513 | chr14 | 104114057 | |||||
chr14:104114263
|
C | T | 2 | a0001c0001t0014a0003c0004t0030 | 4 | NA18941.hp2 NA18985.hp2 NA19060.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1719C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 1719 | chr14 | 104114263 | |||||
chr14:104114735
|
C | T | 3 | a0001c0001t0004a0004c0008t0004a0006c0020t0029 | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2191C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2191 | chr14 | 104114735 | |||||
chr14:104114750
|
G | A | 1 | a0002c0002t0027 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2206G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2206 | chr14 | 104114750 | |||||
chr14:104114852
|
C | T | 2 | a0002c0003t0009a0002c0003t0021 | 8 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2308C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2308 | chr14 | 104114852 | |||||
chr14:104115209
|
G | C | 1 | a0001c0001t0031 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2665G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2665 | chr14 | 104115209 | |||||
chr14:104115233
|
T | A | 2 | a0001c0001t0032a0002c0002t0013 | 4 | HG02132.hp1 NA18949.hp1 NA19003.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2689T>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2689 | chr14 | 104115233 | |||||
chr14:104115323
|
G | C | 14 | a0001c0001t0002a0001c0001t0032a0001c0001t0033others(11): Show | 100 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2779G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2779 | chr14 | 104115323 | |||||
chr14:104115344
|
G | A | 1 | a0001c0006t0028 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2800G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2800 | chr14 | 104115344 | |||||
chr14:104115359
|
G | A | 1 | a0003c0004t0012 | 3 | NA18971.hp1 NA18993.hp2 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2815G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2815 | chr14 | 104115359 | |||||
chr14:104115385
|
C | T | 4 | a0001c0007t0008a0002c0002t0008a0002c0002t0022others(1): Show | 10 | HG02976.hp2 HG03041.hp2 HG03225.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2841C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2841 | chr14 | 104115385 | |||||
chr14:104115388
|
C | G | 9 | a0001c0001t0011a0001c0001t0025a0001c0024t0011others(6): Show | 18 | HG00735.hp1 HG01099.hp2 HG02055.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2844C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2844 | chr14 | 104115388 | |||||
chr14:104115389
|
G | C | 1 | a0001c0001t0034 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2845G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2845 | chr14 | 104115389 | |||||
chr14:104115423
|
A | G | 20 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(17): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2879A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2879 | chr14 | 104115423 | |||||
chr14:104115503
|
T | C | 1 | a0002c0002t0027 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2959T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2959 | chr14 | 104115503 | |||||
chr14:104115547
|
C | A | 1 | a0006c0020t0029 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3003C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 3003 | chr14 | 104115547 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104085866
|
C | T | 1 | a0001c0001t0007g0252 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.82+14C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104085866 | ||||||
chr14:104085964
|
G | A | 1 | a0002c0003t0001g0054 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.82+112G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104085964 | ||||||
chr14:104085983
|
G | A | 5 | a0002c0003t0005g0022a0002c0003t0005g0055a0002c0003t0005g0056others(2): Show | 6 | HG00733.hp1 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+131G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104085983 | ||||||
chr14:104085986
|
C | G | 1 | a0003c0004t0003g0251 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.82+134C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104085986 | ||||||
chr14:104086045
|
A | G | 117 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(114): Show | 165 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(162): Show |
intron_variant | MODIFIER | c.82+193A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086045 | ||||||
chr14:104086132
|
A | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 6 | HG00438.hp2 NA18947.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+280A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086132 | ||||||
chr14:104086265
|
A | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(255): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.82+413A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086265 | ||||||
chr14:104086299
|
G | C | 1 | a0002c0003t0010g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.82+447G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086299 | ||||||
chr14:104086583
|
G | A | 1 | a0005c0021t0003g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.82+731G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086583 | ||||||
chr14:104086749
|
C | T | 1 | a0003c0004t0003g0155 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.82+897C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086749 | ||||||
chr14:104086849
|
C | T | 4 | a0002c0002t0002g0002a0002c0002t0002g0053a0002c0002t0002g0249others(1): Show | 15 | HG00738.hp2 HG01192.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.82+997C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086849 | ||||||
chr14:104086859
|
A | G | 17 | a0001c0001t0004g0052a0001c0001t0004g0242a0001c0001t0010g0246others(14): Show | 22 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.82+1007A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086859 | ||||||
chr14:104086877
|
G | A | 3 | a0002c0002t0002g0161a0002c0002t0015g0040a0002c0002t0015g0160 | 4 | NA18944.hp1 NA18952.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+1025G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086877 | ||||||
chr14:104086983
|
C | T | 1 | a0002c0003t0010g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.82+1131C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086983 | ||||||
chr14:104087184
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(189): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.82+1332A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087184 | ||||||
chr14:104087225
|
TCTC | T | 3 | a0002c0003t0007g0236a0011c0011t0023g0154a0012c0012t0023g0237 | 3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.82+1376_82+1378del others(3): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104087225 | |||||
chr14:104087228
|
C | G | 1 | a0002c0003t0010g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.82+1376C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087228 | ||||||
chr14:104087229
|
C | T | 10 | a0001c0001t0004g0052a0001c0001t0004g0242a0001c0001t0010g0246others(7): Show | 12 | HG00639.hp1 HG01884.hp1 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.82+1377C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087229 | ||||||
chr14:104087273
|
G | A | 10 | a0002c0003t0011g0166a0002c0003t0016g0163a0002c0003t0016g0167others(7): Show | 10 | HG01074.hp1 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.82+1421G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087273 | ||||||
chr14:104087320
|
T | C | 4 | a0002c0002t0002g0172a0002c0002t0002g0173a0002c0002t0019g0174others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+1468T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087320 | ||||||
chr14:104087535
|
G | A | 1 | a0002c0003t0010g0238 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.82+1683G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087535 | ||||||
chr14:104087707
|
G | A | 84 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(81): Show | 127 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.82+1855G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087707 | ||||||
chr14:104087797
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.82+1945C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087797 | ||||||
chr14:104087805
|
C | T | 1 | a0002c0003t0010g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.82+1953C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087805 | ||||||
chr14:104087844
|
G | A | 2 | a0001c0001t0001g0108a0007c0023t0001g0109 | 2 | HG03017.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.82+1992G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087844 | ||||||
chr14:104088098
|
C | T | 1 | a0002c0003t0010g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.82+2246C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088098 | ||||||
chr14:104088103
|
C | G | 10 | a0002c0003t0011g0166a0002c0003t0016g0163a0002c0003t0016g0167others(7): Show | 10 | HG01074.hp1 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.82+2251C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088103 | ||||||
chr14:104088347
|
C | T | 11 | a0001c0001t0001g0153a0002c0003t0011g0166a0002c0003t0016g0163others(8): Show | 11 | HG01074.hp1 HG02109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.82+2495C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088347 | ||||||
chr14:104088502
|
G | A | 3 | a0002c0002t0005g0176a0002c0005t0002g0041a0002c0005t0002g0175 | 4 | HG02809.hp1 HG02970.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+2650G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088502 | ||||||
chr14:104088584
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(189): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.82+2732C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088584 | ||||||
chr14:104088643
|
G | A | 3 | a0002c0002t0002g0172a0002c0002t0002g0173a0002c0002t0019g0174 | 3 | HG02451.hp1 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.82+2791G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088643 | ||||||
chr14:104088784
|
G | A | 3 | a0002c0003t0007g0236a0011c0011t0023g0154a0012c0012t0023g0237 | 3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.82+2932G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088784 | ||||||
chr14:104088788
|
A | G | 2 | a0002c0003t0002g0010a0010c0015t0002g0235 | 5 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+2936A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088788 | ||||||
chr14:104088856
|
G | A | 3 | a0002c0003t0007g0236a0011c0011t0023g0154a0012c0012t0023g0237 | 3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.82+3004G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088856 | ||||||
chr14:104088887
|
G | C | 1 | a0003c0004t0003g0064 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.82+3035G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088887 | ||||||
chr14:104088975
|
T | C | 5 | a0002c0003t0005g0022a0002c0003t0005g0055a0002c0003t0005g0056others(2): Show | 6 | HG00733.hp1 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+3123T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088975 | ||||||
chr14:104088984
|
A | G | 82 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(79): Show | 125 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.82+3132A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088984 | ||||||
chr14:104089002
|
C | T | 1 | a0002c0003t0001g0234 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.82+3150C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089002 | ||||||
chr14:104089096
|
C | T | 66 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0069others(63): Show | 95 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.82+3244C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089096 | ||||||
chr14:104089116
|
G | T | 94 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(91): Show | 137 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.82+3264G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089116 | ||||||
chr14:104089169
|
C | T | 6 | a0001c0001t0010g0246a0001c0001t0011g0244a0001c0001t0025g0243others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+3317C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089169 | ||||||
chr14:104089216
|
G | T | 1 | a0001c0001t0001g0233 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.82+3364G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089216 | ||||||
chr14:104089240
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.82+3388C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089240 | ||||||
chr14:104089327
|
A | C | 1 | a0001c0001t0001g0039 | 2 | NA18963.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.83-3306A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089327 | ||||||
chr14:104089359
|
C | CA | 17 | a0002c0002t0002g0172a0002c0002t0002g0173a0002c0002t0008g0043others(14): Show | 20 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.83-3264dupA | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089359 | |||||
chr14:104089468
|
G | A | 3 | a0001c0001t0011g0244a0001c0001t0025g0243a0001c0019t0010g0245 | 3 | HG02451.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.83-3165G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089468 | ||||||
chr14:104089571
|
C | T | 2 | a0011c0011t0023g0154a0012c0012t0023g0237 | 2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.83-3062C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089571 | ||||||
chr14:104089640
|
G | A | 3 | a0001c0001t0004g0024a0001c0001t0004g0065a0001c0001t0004g0066 | 4 | HG01081.hp1 HG01123.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2993G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089640 | ||||||
chr14:104089792
|
T | A | 3 | a0002c0003t0007g0236a0011c0011t0023g0154a0012c0012t0023g0237 | 3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-2841T>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089792 | ||||||
chr14:104089854
|
A | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0151others(1): Show | 7 | HG00423.hp2 HG02040.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.83-2779A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089854 | ||||||
chr14:104089872
|
G | C | 121 | a0001c0001t0001g0233a0001c0001t0002g0110a0001c0001t0004g0052others(118): Show | 170 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(167): Show |
intron_variant | MODIFIER | c.83-2761G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089872 | ||||||
chr14:104089900
|
A | G | 4 | a0002c0002t0019g0230a0002c0003t0007g0236a0011c0011t0023g0154others(1): Show | 4 | HG01168.hp1 HG02818.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2733A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089900 | ||||||
chr14:104089947
|
C | CA | 49 | a0001c0001t0001g0111a0001c0001t0004g0052a0001c0001t0004g0215others(46): Show | 70 | HG00280.hp2 HG00558.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.83-2659dupA | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | |||||
chr14:104089947
|
C | CAA | 23 | a0001c0001t0004g0242a0001c0001t0010g0246a0002c0002t0002g0002others(20): Show | 36 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.83-2660_83-2659dup others(2): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | |||||
chr14:104089947
|
C | CAAA | 26 | a0002c0002t0002g0004a0002c0002t0002g0018a0002c0002t0002g0045others(23): Show | 37 | HG00609.hp2 HG01074.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.83-2661_83-2659dup others(3): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | |||||
chr14:104089947
|
C | CAAAA | 7 | a0002c0002t0002g0186a0002c0002t0002g0187a0002c0002t0002g0249others(4): Show | 8 | HG01978.hp1 HG02129.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.83-2662_83-2659dup others(4): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | |||||
chr14:104089947
|
CA | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(97): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.83-2659delA | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | |||||
chr14:104089947
|
CAA | C | 8 | a0001c0001t0001g0108a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG01346.hp1 HG01891.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.83-2660_83-2659del others(2): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | |||||
chr14:104089947
|
CAAA | C | 5 | a0002c0003t0005g0022a0002c0003t0005g0056a0002c0003t0005g0057others(2): Show | 6 | HG00733.hp1 HG01884.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-2661_83-2659del others(3): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | |||||
chr14:104090126
|
T | A | 3 | a0002c0002t0002g0018a0002c0002t0002g0189a0002c0002t0002g0201 | 5 | HG02015.hp1 NA18962.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-2507T>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090126 | ||||||
chr14:104090394
|
C | T | 1 | a0002c0002t0022g0038 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.83-2239C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090394 | ||||||
chr14:104090431
|
C | T | 1 | a0001c0001t0005g0061 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.83-2202C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090431 | ||||||
chr14:104090519
|
G | T | 2 | a0002c0003t0002g0178a0002c0003t0018g0177 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.83-2114G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090519 | ||||||
chr14:104090539
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.83-2094G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090539 | ||||||
chr14:104090553
|
C | T | 10 | a0002c0003t0011g0166a0002c0003t0016g0163a0002c0003t0016g0167others(7): Show | 10 | HG01074.hp1 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.83-2080C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090553 | ||||||
chr14:104090567
|
C | T | 2 | a0002c0003t0009g0182a0002c0003t0009g0183 | 2 | HG00280.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.83-2066C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090567 | ||||||
chr14:104090695
|
C | T | 8 | a0002c0003t0005g0184a0002c0003t0009g0042a0002c0003t0009g0179others(5): Show | 9 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.83-1938C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090695 | ||||||
chr14:104090773
|
A | C | 2 | a0002c0003t0002g0178a0002c0003t0018g0177 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.83-1860A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090773 | ||||||
chr14:104090935
|
G | C | 3 | a0002c0003t0007g0236a0011c0011t0023g0154a0012c0012t0023g0237 | 3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-1698G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090935 | ||||||
chr14:104090969
|
G | T | 1 | a0002c0003t0007g0236 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.83-1664G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090969 | ||||||
chr14:104090970
|
A | C | 75 | a0001c0001t0001g0233a0002c0002t0002g0002a0002c0002t0002g0004others(72): Show | 118 | HG00558.hp2 HG00609.hp2 HG00738.hp2 others(115): Show |
intron_variant | MODIFIER | c.83-1663A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090970 | ||||||
chr14:104091105
|
A | G | 3 | a0002c0003t0007g0236a0011c0011t0023g0154a0012c0012t0023g0237 | 3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-1528A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091105 | ||||||
chr14:104091323
|
G | C | 5 | a0002c0003t0005g0022a0002c0003t0005g0055a0002c0003t0005g0056others(2): Show | 6 | HG00733.hp1 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-1310G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091323 | ||||||
chr14:104091388
|
G | C | 3 | a0002c0003t0007g0236a0011c0011t0023g0154a0012c0012t0023g0237 | 3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-1245G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091388 | ||||||
chr14:104091458
|
C | G | 1 | a0001c0001t0001g0146 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.83-1175C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091458 | ||||||
chr14:104091458
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.83-1175C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091458 | ||||||
chr14:104091574
|
C | T | 7 | a0001c0001t0001g0105a0001c0006t0002g0033a0002c0003t0002g0178others(4): Show | 8 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.83-1059C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091574 | ||||||
chr14:104091575
|
G | A | 1 | a0002c0003t0007g0236 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.83-1058G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091575 | ||||||
chr14:104091599
|
G | A | 1 | a0011c0011t0023g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.83-1034G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091599 | ||||||
chr14:104091603
|
T | C | 1 | a0002c0003t0010g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.83-1030T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091603 | ||||||
chr14:104091652
|
C | T | 3 | a0001c0001t0011g0244a0001c0001t0025g0243a0001c0019t0010g0245 | 3 | HG02451.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.83-981C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091652 | ||||||
chr14:104091695
|
T | C | 1 | a0001c0001t0004g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.83-938T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091695 | ||||||
chr14:104091749
|
G | A | 1 | a0002c0003t0001g0216 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.83-884G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091749 | ||||||
chr14:104091826
|
C | T | 1 | a0002c0002t0002g0200 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.83-807C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091826 | ||||||
chr14:104091982
|
T | C | 107 | a0002c0002t0002g0002a0002c0002t0002g0004a0002c0002t0002g0006others(104): Show | 155 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(152): Show |
intron_variant | MODIFIER | c.83-651T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091982 | ||||||
chr14:104092002
|
C | A | 1 | a0002c0003t0010g0238 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.83-631C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104092002 | ||||||
chr14:104092390
|
C | T | 3 | a0002c0003t0007g0236a0011c0011t0023g0154a0012c0012t0023g0237 | 3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-243C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104092390 | ||||||
chr14:104092400
|
C | T | 1 | a0002c0003t0016g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.83-233C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104092400 | ||||||
chr14:104092451
|
C | T | 3 | a0002c0003t0007g0236a0011c0011t0023g0154a0012c0012t0023g0237 | 3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-182C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104092451 | ||||||
chr14:104093012
|
C | T | 15 | a0002c0003t0005g0184a0002c0003t0006g0049a0002c0003t0006g0050others(12): Show | 19 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.191+271C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093012 | ||||||
chr14:104093015
|
C | T | 1 | a0002c0003t0010g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.191+274C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093015 | ||||||
chr14:104093026
|
C | A | 6 | a0002c0003t0006g0049a0002c0003t0006g0050a0002c0003t0006g0051others(3): Show | 9 | HG00735.hp1 HG01099.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.191+285C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093026 | ||||||
chr14:104093142
|
A | C | 1 | a0002c0002t0002g0199 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.192-349A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093142 | ||||||
chr14:104093169
|
C | T | 110 | a0002c0002t0002g0002a0002c0002t0002g0004a0002c0002t0002g0006others(107): Show | 158 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(155): Show |
intron_variant | MODIFIER | c.192-322C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093169 | ||||||
chr14:104093183
|
G | A | 2 | a0002c0002t0002g0202a0002c0002t0002g0203 | 2 | HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.192-308G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093183 | ||||||
chr14:104093215
|
G | C | 110 | a0002c0002t0002g0002a0002c0002t0002g0004a0002c0002t0002g0006others(107): Show | 158 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(155): Show |
intron_variant | MODIFIER | c.192-276G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093215 | ||||||
chr14:104093286
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(202): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.192-205T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093286 | ||||||
chr14:104093311
|
C | T | 3 | a0002c0003t0007g0236a0011c0011t0023g0154a0012c0012t0023g0237 | 3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.192-180C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093311 | ||||||
chr14:104093328
|
C | T | 1 | a0004c0008t0004g0021 | 3 | HG00639.hp1 HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.192-163C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093328 | ||||||
chr14:104093335
|
C | T | 1 | a0011c0011t0023g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.192-156C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093335 | ||||||
chr14:104093622
|
CTGGGTGG others(31): Show |
C | 107 | a0002c0002t0002g0002a0002c0002t0002g0004a0002c0002t0002g0006others(104): Show | 155 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(152): Show |
intron_variant | MODIFIER | c.303+52_303+89delAG others(36): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 104093622 | |||||
chr14:104093654
|
A | T | 3 | a0002c0003t0007g0236a0011c0011t0023g0154a0012c0012t0023g0237 | 3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.303+52A>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104093654 | ||||||
chr14:104093660
|
G | GTGGGTGG others(13): Show |
3 | a0002c0003t0007g0236a0011c0011t0023g0154a0012c0012t0023g0237 | 3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.303+70_303+71insGG others(18): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 104093660 | |||||
chr14:104093806
|
G | A | 1 | a0003c0004t0003g0088 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.303+204G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104093806 | ||||||
chr14:104093857
|
G | A | 1 | a0002c0003t0010g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.303+255G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104093857 | ||||||
chr14:104093889
|
GGTGGGGC others(10): Show |
G | 1 | a0002c0002t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.303+298_303+314del others(17): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 104093889 | |||||
chr14:104093964
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.303+362G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104093964 | ||||||
chr14:104094140
|
C | T | 1 | a0002c0003t0017g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.303+538C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094140 | ||||||
chr14:104094149
|
A | G | 1 | a0002c0003t0017g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.303+547A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094149 | ||||||
chr14:104094163
|
G | A | 1 | a0002c0002t0002g0217 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.303+561G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094163 | ||||||
chr14:104094193
|
G | A | 1 | a0001c0001t0031g0148 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.303+591G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094193 | ||||||
chr14:104094201
|
G | A | 1 | a0001c0007t0002g0248 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.303+599G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094201 | ||||||
chr14:104094252
|
G | A | 1 | a0002c0002t0002g0218 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.303+650G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094252 | ||||||
chr14:104094374
|
T | G | 1 | a0002c0002t0002g0219 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.303+772T>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094374 | ||||||
chr14:104094487
|
C | T | 1 | a0002c0002t0019g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.303+885C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094487 | ||||||
chr14:104094512
|
C | T | 1 | a0002c0003t0037g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.303+910C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094512 | ||||||
chr14:104094533
|
G | A | 68 | a0001c0001t0004g0090a0001c0006t0002g0033a0002c0002t0002g0002others(65): Show | 108 | HG00558.hp2 HG00609.hp2 HG00738.hp2 others(105): Show |
intron_variant | MODIFIER | c.303+931G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094533 | ||||||
chr14:104094558
|
A | G | 1 | a0002c0013t0039g0168 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.303+956A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094558 | ||||||
chr14:104094675
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(212): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.304-856A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094675 | ||||||
chr14:104094881
|
C | T | 4 | a0002c0002t0002g0045a0002c0002t0013g0188a0002c0002t0013g0197others(1): Show | 5 | HG02040.hp2 HG02071.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-650C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094881 | ||||||
chr14:104095148
|
C | T | 1 | a0003c0004t0003g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.304-383C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095148 | ||||||
chr14:104095260
|
T | C | 3 | a0002c0003t0009g0042a0011c0011t0023g0154a0012c0012t0023g0237 | 4 | HG01168.hp1 HG02735.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-271T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095260 | ||||||
chr14:104095302
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.304-229G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095302 | ||||||
chr14:104095348
|
C | T | 2 | a0002c0002t0002g0219a0002c0002t0002g0226 | 2 | HG00558.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.304-183C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095348 | ||||||
chr14:104095354
|
A | G | 1 | a0003c0004t0003g0107 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.304-177A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095354 | ||||||
chr14:104095375
|
G | A | 14 | a0001c0001t0001g0083a0001c0001t0007g0025a0001c0001t0007g0078others(11): Show | 16 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.304-156G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095375 | ||||||
chr14:104095514
|
A | C | 3 | a0002c0003t0018g0181a0002c0003t0021g0180a0002c0003t0021g0185 | 3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.304-17A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095514 | ||||||
chr14:104095661
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(208): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
splice_region_variant&intron_variant | LOW | c.429+5T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095661 | ||||||
chr14:104095716
|
C | T | 1 | a0001c0001t0004g0032 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.429+60C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095716 | ||||||
chr14:104095723
|
G | A | 11 | a0001c0001t0007g0025a0001c0001t0007g0078a0002c0003t0005g0184others(8): Show | 13 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+67G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095723 | ||||||
chr14:104095746
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0124 | 2 | NA18949.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.429+90G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095746 | ||||||
chr14:104095852
|
A | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(253): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.429+196A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095852 | ||||||
chr14:104095925
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.429+269C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095925 | ||||||
chr14:104095963
|
G | GATGCTTC others(19): Show |
1 | a0002c0003t0005g0056 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.429+308_429+333dup others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 104095963 | |||||
chr14:104095975
|
C | T | 3 | a0001c0001t0004g0242a0001c0019t0010g0245a0004c0008t0004g0021 | 5 | HG00639.hp1 HG01884.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+319C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095975 | ||||||
chr14:104096017
|
C | T | 1 | a0002c0002t0002g0214 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.429+361C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096017 | ||||||
chr14:104096027
|
C | T | 1 | a0002c0002t0002g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.429+371C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096027 | ||||||
chr14:104096139
|
C | A | 1 | a0001c0019t0010g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.429+483C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096139 | ||||||
chr14:104096244
|
G | A | 9 | a0002c0003t0002g0178a0002c0003t0006g0049a0002c0003t0006g0050others(6): Show | 12 | HG00735.hp1 HG01099.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.429+588G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096244 | ||||||
chr14:104096261
|
G | A | 5 | a0002c0003t0005g0022a0002c0003t0005g0055a0002c0003t0005g0056others(2): Show | 6 | HG00733.hp1 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+605G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096261 | ||||||
chr14:104096475
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(99): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.429+819A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096475 | ||||||
chr14:104096499
|
C | A | 3 | a0002c0003t0005g0022a0002c0003t0005g0056a0002c0003t0005g0057 | 4 | HG00733.hp1 HG01884.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+843C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096499 | ||||||
chr14:104096501
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.429+845C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096501 | ||||||
chr14:104096549
|
G | C | 7 | a0001c0007t0002g0248a0001c0007t0008g0067a0001c0007t0008g0079others(4): Show | 8 | HG02615.hp2 HG02976.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+893G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096549 | ||||||
chr14:104096681
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(210): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.430-873A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096681 | ||||||
chr14:104096769
|
C | A | 3 | a0002c0003t0006g0049a0002c0003t0006g0239a0002c0026t0006g0220 | 4 | HG02055.hp1 HG02258.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-785C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096769 | ||||||
chr14:104096778
|
A | C | 4 | a0002c0003t0006g0050a0002c0003t0006g0051a0002c0003t0006g0240others(1): Show | 6 | HG00735.hp1 HG01099.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-776A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096778 | ||||||
chr14:104096832
|
A | G | 2 | a0001c0001t0001g0144a0002c0003t0001g0216 | 2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.430-722A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096832 | ||||||
chr14:104096865
|
C | T | 2 | a0011c0011t0023g0154a0012c0012t0023g0237 | 2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.430-689C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096865 | ||||||
chr14:104096994
|
G | A | 1 | a0002c0002t0022g0038 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.430-560G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096994 | ||||||
chr14:104097020
|
C | T | 1 | a0001c0001t0005g0023 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.430-534C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097020 | ||||||
chr14:104097113
|
G | T | 1 | a0003c0004t0003g0064 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.430-441G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097113 | ||||||
chr14:104097126
|
G | A | 5 | a0002c0003t0001g0019a0002c0003t0001g0044a0002c0003t0001g0054others(2): Show | 8 | HG01074.hp2 HG01167.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-428G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097126 | ||||||
chr14:104097273
|
G | A | 1 | a0002c0002t0002g0219 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.430-281G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097273 | ||||||
chr14:104097322
|
G | A | 6 | a0001c0007t0002g0248a0001c0007t0008g0067a0001c0007t0008g0079others(3): Show | 7 | HG02615.hp2 HG02976.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-232G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097322 | ||||||
chr14:104097323
|
T | A | 1 | a0001c0019t0010g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.430-231T>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097323 | ||||||
chr14:104097345
|
G | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(90): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.430-209G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097345 | ||||||
chr14:104097414
|
C | T | 1 | a0002c0003t0009g0179 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.430-140C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097414 | ||||||
chr14:104097421
|
C | T | 7 | a0001c0007t0002g0248a0001c0007t0008g0067a0001c0007t0008g0079others(4): Show | 8 | HG02615.hp2 HG02976.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-133C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097421 | ||||||
chr14:104097537
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(101): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.430-17C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097537 | ||||||
chr14:104097676
|
T | G | 2 | a0002c0002t0002g0186a0002c0002t0002g0190 | 2 | NA18999.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.513+39T>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097676 | ||||||
chr14:104097809
|
AGTTCTAC others(45): Show |
A | 9 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0065others(6): Show | 13 | HG01081.hp1 HG01123.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.513+217_513+268del others(52): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097809 | |||||
chr14:104097813
|
CTACGTTA others(383): Show |
C | 1 | a0001c0001t0011g0244 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.513+202_513+591del | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097813 | |||||
chr14:104097815
|
ACGTTAGA others(97): Show |
A | 2 | a0002c0003t0002g0178a0002c0003t0018g0177 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.513+189_513+292del | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097815 | |||||
chr14:104097826
|
A | ACGTATGG others(19): Show |
2 | a0001c0006t0002g0125a0003c0025t0003g0084 | 2 | HG02145.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.513+191_513+216dup others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097826 | |||||
chr14:104097826
|
ACGTATGG others(71): Show |
A | 4 | a0001c0001t0001g0083a0001c0001t0001g0138a0001c0001t0001g0140others(1): Show | 4 | HG01099.hp1 HG01934.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+217_513+294del others(78): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097826 | |||||
chr14:104097826
|
ACGTATGG others(123): Show |
A | 5 | a0001c0001t0001g0141a0002c0003t0006g0050a0002c0003t0006g0051others(2): Show | 7 | HG00735.hp1 HG01099.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.513+217_513+346del | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097826 | |||||
chr14:104097846
|
A | AGAGATGC others(19): Show |
1 | a0001c0006t0002g0126 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.513+216_513+217ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097846 | |||||
chr14:104097852
|
G | GCGTATGG others(45): Show |
1 | a0002c0002t0002g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.513+216_513+217ins others(52): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097852 | |||||
chr14:104097852
|
GCATATGG others(19): Show |
G | 5 | a0001c0001t0001g0123a0001c0001t0001g0142a0001c0001t0001g0144others(2): Show | 5 | HG02602.hp1 HG02738.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+217_513+242del others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097852 | |||||
chr14:104097854
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(156): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.513+217A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097854 | ||||||
chr14:104097867
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(155): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.513+230A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097867 | ||||||
chr14:104097878
|
A | ACGTATGG others(19): Show |
3 | a0001c0001t0004g0028a0001c0001t0004g0032a0003c0004t0003g0007 | 8 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+283_513+308dup others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097878 | |||||
chr14:104097878
|
A | G | 62 | a0001c0006t0028g0143a0001c0019t0010g0245a0002c0002t0002g0002others(59): Show | 98 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.513+241A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097878 | ||||||
chr14:104097891
|
C | CTGCGTTA others(45): Show |
4 | a0002c0002t0002g0222a0002c0005t0002g0223a0002c0005t0008g0213others(1): Show | 4 | HG02109.hp1 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+266_513+267ins others(52): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097891 | |||||
chr14:104097891
|
C | CTGCGTTA others(71): Show |
1 | a0002c0002t0002g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+266_513+267ins others(78): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097891 | |||||
chr14:104097891
|
C | T | 3 | a0002c0002t0002g0199a0002c0002t0002g0209a0002c0002t0002g0225 | 3 | HG02738.hp2 HG03834.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.513+254C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097891 | ||||||
chr14:104097894
|
C | T | 5 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0065others(2): Show | 8 | HG01081.hp1 HG01123.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+257C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097894 | ||||||
chr14:104097904
|
G | A | 57 | a0001c0001t0010g0246a0001c0006t0028g0143a0001c0019t0010g0245others(54): Show | 93 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.513+267G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097904 | ||||||
chr14:104097917
|
C | CTGCGTTA others(97): Show |
2 | a0003c0004t0003g0073a0003c0004t0003g0094 | 2 | HG02080.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.513+308_513+309ins others(104): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097917 | |||||
chr14:104097917
|
C | CTGCGTTA others(19): Show |
1 | a0002c0002t0002g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+305_513+306ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097917 | |||||
chr14:104097917
|
C | T | 8 | a0001c0006t0002g0033a0001c0006t0002g0125a0001c0006t0002g0126others(5): Show | 10 | HG01433.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.513+280C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097917 | ||||||
chr14:104097920
|
C | T | 2 | a0003c0004t0003g0103a0003c0004t0003g0104 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.513+283C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097920 | ||||||
chr14:104097920
|
CGTTAGAG others(19): Show |
C | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(62): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.513+309_513+334del others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097920 | |||||
chr14:104097930
|
G | GCGTATGG others(19): Show |
1 | a0002c0003t0010g0238 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.513+307_513+308ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097930 | |||||
chr14:104097943
|
C | T | 49 | a0001c0006t0002g0126a0001c0006t0028g0143a0002c0002t0002g0002others(46): Show | 83 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.513+306C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097943 | ||||||
chr14:104097945
|
G | A | 3 | a0001c0001t0010g0246a0002c0003t0010g0159a0002c0003t0037g0169 | 3 | HG02572.hp1 HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.513+308G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097945 | ||||||
chr14:104097946
|
T | C | 155 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0087others(152): Show | 217 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.513+309T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097946 | ||||||
chr14:104097956
|
G | A | 39 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0087others(36): Show | 46 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.513+319G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097956 | ||||||
chr14:104097956
|
G | GCATATGG others(19): Show |
1 | a0001c0019t0010g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.513+320_513+321ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097956 | |||||
chr14:104097969
|
C | T | 25 | a0001c0001t0025g0243a0002c0002t0002g0004a0002c0002t0002g0006others(22): Show | 42 | HG00558.hp2 HG01123.hp2 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.513+332C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097969 | ||||||
chr14:104097972
|
C | CGTTAGAG others(19): Show |
2 | a0011c0011t0023g0154a0012c0012t0023g0237 | 2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.513+360_513+361ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097972 | |||||
chr14:104097982
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(68): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.513+345G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097982 | ||||||
chr14:104097995
|
C | T | 5 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0065others(2): Show | 8 | HG01081.hp1 HG01123.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+358C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097995 | ||||||
chr14:104097997
|
G | A | 2 | a0001c0001t0025g0243a0002c0003t0011g0166 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.513+360G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097997 | ||||||
chr14:104098009
|
C | T | 2 | a0001c0001t0010g0246a0002c0003t0010g0159 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.513+372C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098009 | ||||||
chr14:104098021
|
C | CTGCGTTA others(19): Show |
1 | a0003c0004t0003g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.513+436_513+461dup others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098021 | |||||
chr14:104098021
|
C | T | 22 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0052others(19): Show | 30 | HG00639.hp1 HG00735.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.513+384C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098021 | ||||||
chr14:104098021
|
CTGCGTTA others(19): Show |
C | 17 | a0001c0001t0001g0083a0001c0001t0001g0123a0001c0001t0001g0138others(14): Show | 22 | HG00423.hp2 HG01074.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.513+436_513+461del others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098021 | |||||
chr14:104098021
|
CTGCGTTA others(45): Show |
C | 4 | a0001c0001t0001g0116a0001c0001t0001g0139a0001c0001t0025g0243others(1): Show | 4 | HG01981.hp1 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+410_513+461del others(52): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098021 | |||||
chr14:104098023
|
G | A | 1 | a0001c0019t0010g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.513+386G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098023 | ||||||
chr14:104098024
|
C | T | 2 | a0011c0011t0023g0154a0012c0012t0023g0237 | 2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.513+387C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098024 | ||||||
chr14:104098034
|
G | A | 1 | a0001c0019t0010g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.513+397G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098034 | ||||||
chr14:104098034
|
GCGTATGG others(97): Show |
G | 2 | a0001c0001t0001g0071a0001c0001t0001g0087 | 2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.513+410_513+513del | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098034 | |||||
chr14:104098047
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(160): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.513+410T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098047 | ||||||
chr14:104098049
|
G | A | 16 | a0001c0001t0001g0141a0001c0001t0004g0052a0001c0001t0004g0242others(13): Show | 21 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.513+412G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098049 | ||||||
chr14:104098061
|
C | T | 1 | a0001c0001t0014g0035 | 2 | NA18985.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.513+424C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098061 | ||||||
chr14:104098062
|
G | A | 8 | a0001c0001t0001g0141a0001c0001t0004g0052a0001c0001t0004g0242others(5): Show | 10 | HG00639.hp1 HG01884.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+425G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098062 | ||||||
chr14:104098073
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(191): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.513+436T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098073 | ||||||
chr14:104098073
|
TTGCGTTA others(19): Show |
T | 2 | a0001c0001t0001g0141a0002c0003t0007g0236 | 2 | NA18943.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.513+464_513+489del others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098073 | |||||
chr14:104098075
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(96): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.513+438G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098075 | ||||||
chr14:104098075
|
G | C | 24 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0052others(21): Show | 32 | HG00639.hp1 HG00735.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.513+438G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098075 | ||||||
chr14:104098088
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(85): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.513+451G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098088 | ||||||
chr14:104098099
|
C | A | 24 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0052others(21): Show | 32 | HG00639.hp1 HG00735.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.513+462C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098099 | ||||||
chr14:104098099
|
C | T | 27 | a0001c0001t0004g0215a0002c0002t0002g0004a0002c0002t0002g0006others(24): Show | 46 | HG00558.hp2 HG01123.hp2 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.513+462C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098099 | ||||||
chr14:104098101
|
G | A | 53 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0052others(50): Show | 68 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.513+464G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098101 | ||||||
chr14:104098101
|
G | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(119): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.513+464G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098101 | ||||||
chr14:104098103
|
G | C | 24 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0052others(21): Show | 32 | HG00639.hp1 HG00735.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.513+466G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098103 | ||||||
chr14:104098112
|
G | A | 22 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0065others(19): Show | 30 | HG00639.hp1 HG00735.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.513+475G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098112 | ||||||
chr14:104098112
|
G | GCGTATGG others(19): Show |
25 | a0001c0006t0028g0143a0001c0007t0008g0247a0002c0002t0002g0002others(22): Show | 39 | HG00280.hp2 HG00609.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.513+487_513+488ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | |||||
chr14:104098112
|
G | GCGTATGG others(97): Show |
3 | a0002c0005t0002g0223a0002c0005t0008g0213a0002c0005t0008g0228 | 3 | HG02109.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.513+487_513+488ins others(104): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | |||||
chr14:104098112
|
G | GCGTATGG others(71): Show |
25 | a0002c0002t0002g0004a0002c0002t0002g0006a0002c0002t0002g0009others(22): Show | 43 | HG00558.hp2 HG01123.hp2 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.513+489_513+490ins others(78): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | |||||
chr14:104098112
|
G | GCGTATGG others(149): Show |
3 | a0002c0002t0005g0176a0002c0005t0002g0041a0002c0005t0002g0175 | 4 | HG02809.hp1 HG02970.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+489_513+490ins others(156): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | |||||
chr14:104098112
|
G | GCGTATGG others(97): Show |
1 | a0001c0019t0010g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.513+489_513+490ins others(104): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | |||||
chr14:104098112
|
G | GCGTATGG others(149): Show |
2 | a0002c0002t0008g0043a0002c0016t0006g0212 | 3 | HG02970.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.513+489_513+490ins others(156): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | |||||
chr14:104098112
|
G | GCGTATGG others(123): Show |
1 | a0002c0002t0019g0230 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.513+489_513+490ins others(130): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | |||||
chr14:104098112
|
G | GCGTATGG others(97): Show |
2 | a0001c0001t0004g0215a0003c0004t0003g0095 | 2 | HG02895.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.513+487_513+488ins others(104): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | |||||
chr14:104098125
|
C | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(92): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.513+488C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098125 | ||||||
chr14:104098127
|
C | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(176): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.513+490C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098127 | ||||||
chr14:104098127
|
C | CCGTTAGA others(45): Show |
68 | a0001c0001t0004g0028a0001c0001t0004g0031a0001c0001t0004g0032others(65): Show | 93 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.513+500_513+501ins others(52): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098127 | |||||
chr14:104098127
|
C | G | 2 | a0001c0001t0004g0052a0006c0020t0029g0052 | 2 | HG02273.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.513+490C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098127 | ||||||
chr14:104098128
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.513+491C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098128 | ||||||
chr14:104098129
|
G | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(90): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.513+492G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098129 | ||||||
chr14:104098129
|
G | CTTAGAGA others(19): Show |
2 | a0001c0007t0002g0248a0001c0007t0008g0080 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.513+491_513+492ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098129 | ||||||
chr14:104098129
|
G | GTTAGAGA others(19): Show |
9 | a0002c0003t0005g0022a0002c0003t0005g0055a0002c0003t0005g0056others(6): Show | 12 | HG00733.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.513+500_513+501ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098129 | |||||
chr14:104098153
|
G | A | 11 | a0001c0001t0001g0071a0001c0001t0001g0087a0002c0003t0005g0022others(8): Show | 14 | HG00140.hp1 HG00733.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.513+516G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098153 | ||||||
chr14:104098153
|
G | ACGTTAGA others(19): Show |
2 | a0001c0007t0008g0067a0001c0007t0008g0079 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.513+515_513+516ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098153 | ||||||
chr14:104098164
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0087 | 2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.513+527A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098164 | ||||||
chr14:104098166
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0087 | 2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.513+529G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098166 | ||||||
chr14:104098179
|
G | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0087 | 2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.513+542G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098179 | ||||||
chr14:104098190
|
G | A | 1 | a0001c0006t0002g0126 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.513+553G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098190 | ||||||
chr14:104098216
|
A | G | 1 | a0001c0006t0002g0126 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.513+579A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098216 | ||||||
chr14:104098233
|
A | G | 1 | a0001c0006t0002g0126 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.513+596A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098233 | ||||||
chr14:104098243
|
G | C | 1 | a0001c0006t0002g0126 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.513+606G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098243 | ||||||
chr14:104098388
|
C | T | 1 | a0002c0002t0002g0194 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.514-465C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098388 | ||||||
chr14:104098642
|
C | T | 1 | a0003c0004t0003g0093 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.514-211C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098642 | ||||||
chr14:104098712
|
C | G | 1 | a0002c0003t0009g0182 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.514-141C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098712 | ||||||
chr14:104098721
|
C | A | 8 | a0001c0001t0011g0244a0001c0001t0025g0243a0001c0024t0011g0060others(5): Show | 8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-132C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098721 | ||||||
chr14:104098753
|
G | A | 2 | a0011c0011t0023g0154a0012c0012t0023g0237 | 2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.514-100G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098753 | ||||||
chr14:104099315
|
A | T | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.640+336A>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099315 | ||||||
chr14:104099385
|
GC | G | 8 | a0001c0001t0011g0244a0001c0001t0025g0243a0001c0024t0011g0060others(5): Show | 8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.640+409delC | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 104099385 | |||||
chr14:104099414
|
G | T | 8 | a0001c0001t0011g0244a0001c0001t0025g0243a0001c0024t0011g0060others(5): Show | 8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.640+435G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099414 | ||||||
chr14:104099442
|
G | T | 65 | a0001c0001t0002g0110a0001c0006t0002g0033a0001c0006t0002g0125others(62): Show | 103 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(100): Show |
intron_variant | MODIFIER | c.640+463G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099442 | ||||||
chr14:104099534
|
C | T | 4 | a0002c0002t0002g0002a0002c0002t0002g0053a0002c0002t0002g0249others(1): Show | 15 | HG00738.hp2 HG01192.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.640+555C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099534 | ||||||
chr14:104099535
|
G | A | 1 | a0001c0022t0001g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.640+556G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099535 | ||||||
chr14:104099585
|
G | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(211): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.640+606G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099585 | ||||||
chr14:104099590
|
G | A | 1 | a0002c0002t0027g0204 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.640+611G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099590 | ||||||
chr14:104099652
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(131): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.640+673T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099652 | ||||||
chr14:104099782
|
C | T | 98 | a0001c0001t0002g0110a0001c0001t0004g0013a0001c0001t0004g0024others(95): Show | 148 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(145): Show |
intron_variant | MODIFIER | c.640+803C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099782 | ||||||
chr14:104099784
|
C | T | 1 | a0001c0027t0001g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.640+805C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099784 | ||||||
chr14:104099834
|
G | A | 8 | a0001c0001t0011g0244a0001c0001t0025g0243a0001c0024t0011g0060others(5): Show | 8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.640+855G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099834 | ||||||
chr14:104099907
|
G | A | 1 | a0003c0004t0012g0011 | 3 | NA18971.hp1 NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.640+928G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099907 | ||||||
chr14:104099946
|
C | T | 17 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0028others(14): Show | 26 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.640+967C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099946 | ||||||
chr14:104100166
|
G | A | 1 | a0002c0002t0002g0202 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.640+1187G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100166 | ||||||
chr14:104100213
|
T | C | 4 | a0002c0002t0002g0004a0002c0002t0002g0187a0002c0002t0002g0199others(1): Show | 10 | NA18941.hp1 NA18945.hp1 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+1234T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100213 | ||||||
chr14:104100251
|
G | T | 2 | a0003c0004t0003g0103a0003c0004t0003g0104 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.640+1272G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100251 | ||||||
chr14:104100333
|
G | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 9 | HG00639.hp2 HG01928.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.640+1354G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100333 | ||||||
chr14:104100356
|
C | T | 2 | a0002c0002t0002g0189a0002c0002t0002g0201 | 2 | NA18962.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.640+1377C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100356 | ||||||
chr14:104100433
|
A | G | 74 | a0001c0001t0002g0110a0001c0006t0002g0033a0001c0006t0002g0125others(71): Show | 113 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.640+1454A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100433 | ||||||
chr14:104100575
|
C | T | 26 | a0003c0004t0003g0003a0003c0004t0003g0007a0003c0004t0003g0012others(23): Show | 42 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.640+1596C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100575 | ||||||
chr14:104100862
|
G | T | 1 | a0010c0015t0002g0235 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.640+1883G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100862 | ||||||
chr14:104100879
|
C | T | 11 | a0001c0001t0007g0025a0001c0001t0007g0078a0002c0003t0005g0184others(8): Show | 13 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.640+1900C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100879 | ||||||
chr14:104101008
|
G | A | 1 | a0001c0001t0010g0246 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.640+2029G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101008 | ||||||
chr14:104101049
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0153 | 3 | NA18997.hp1 NA19060.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.640+2070G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101049 | ||||||
chr14:104101085
|
G | A | 36 | a0002c0013t0039g0168a0003c0004t0003g0003a0003c0004t0003g0007others(33): Show | 52 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.640+2106G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101085 | ||||||
chr14:104101116
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.640+2137G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101116 | ||||||
chr14:104101158
|
G | A | 1 | a0001c0001t0004g0066 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.640+2179G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101158 | ||||||
chr14:104101173
|
A | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(253): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.640+2194A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101173 | ||||||
chr14:104101188
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(217): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.640+2209C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101188 | ||||||
chr14:104101239
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(217): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.640+2260C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101239 | ||||||
chr14:104101306
|
G | C | 58 | a0001c0001t0002g0110a0001c0006t0002g0033a0001c0006t0002g0125others(55): Show | 95 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.641-2257G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101306 | ||||||
chr14:104101385
|
C | T | 127 | a0001c0001t0002g0110a0001c0001t0004g0013a0001c0001t0004g0024others(124): Show | 180 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(177): Show |
intron_variant | MODIFIER | c.641-2178C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101385 | ||||||
chr14:104101482
|
G | T | 1 | a0002c0002t0002g0047 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.641-2081G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101482 | ||||||
chr14:104101585
|
C | T | 2 | a0002c0003t0006g0240a0002c0003t0006g0241 | 2 | HG00735.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.641-1978C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101585 | ||||||
chr14:104101589
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(217): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.641-1974G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101589 | ||||||
chr14:104101595
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(217): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.641-1968A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101595 | ||||||
chr14:104101599
|
C | G | 8 | a0001c0001t0011g0244a0001c0001t0025g0243a0001c0024t0011g0060others(5): Show | 8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-1964C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101599 | ||||||
chr14:104101693
|
T | C | 1 | a0010c0015t0002g0235 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.641-1870T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101693 | ||||||
chr14:104101756
|
ACCTC | A | 9 | a0002c0003t0002g0178a0002c0003t0006g0049a0002c0003t0006g0050others(6): Show | 12 | HG00735.hp1 HG01099.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.641-1800_641-1797d others(6): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 104101756 | |||||
chr14:104101804
|
C | A | 1 | a0002c0002t0002g0161 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.641-1759C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101804 | ||||||
chr14:104101815
|
C | A | 1 | a0001c0022t0001g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.641-1748C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101815 | ||||||
chr14:104101831
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.641-1732G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101831 | ||||||
chr14:104102130
|
T | C | 1 | a0010c0015t0002g0235 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.641-1433T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102130 | ||||||
chr14:104102135
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(217): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.641-1428T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102135 | ||||||
chr14:104102279
|
C | A | 1 | a0001c0001t0004g0031 | 2 | HG01255.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.641-1284C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102279 | ||||||
chr14:104102279
|
C | G | 1 | a0002c0013t0039g0168 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.641-1284C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102279 | ||||||
chr14:104102367
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.641-1196G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102367 | ||||||
chr14:104102376
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.641-1187C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102376 | ||||||
chr14:104102591
|
C | A | 1 | a0010c0015t0002g0235 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.641-972C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102591 | ||||||
chr14:104102600
|
C | G | 1 | a0002c0002t0019g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.641-963C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102600 | ||||||
chr14:104102692
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.641-871C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102692 | ||||||
chr14:104102743
|
G | A | 1 | a0001c0019t0010g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.641-820G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102743 | ||||||
chr14:104102788
|
G | C | 11 | a0001c0001t0007g0025a0001c0001t0007g0078a0002c0003t0005g0184others(8): Show | 13 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.641-775G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102788 | ||||||
chr14:104102819
|
C | G | 1 | a0001c0001t0001g0157 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.641-744C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102819 | ||||||
chr14:104103015
|
C | T | 1 | a0001c0001t0005g0061 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.641-548C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103015 | ||||||
chr14:104103129
|
T | C | 3 | a0001c0001t0011g0244a0001c0001t0025g0243a0002c0003t0011g0166 | 3 | HG02647.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.641-434T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103129 | ||||||
chr14:104103148
|
C | T | 1 | a0001c0001t0033g0134 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.641-415C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103148 | ||||||
chr14:104103151
|
G | A | 1 | a0002c0003t0017g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.641-412G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103151 | ||||||
chr14:104103182
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0035g0133 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.641-381C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103182 | ||||||
chr14:104103192
|
C | T | 1 | a0002c0003t0005g0184 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.641-371C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103192 | ||||||
chr14:104103242
|
C | CG | 3 | a0001c0001t0011g0244a0001c0001t0025g0243a0002c0003t0011g0166 | 3 | HG02647.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.641-321_641-320ins others(1): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103242 | ||||||
chr14:104103308
|
C | T | 1 | a0001c0007t0008g0247 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.641-255C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103308 | ||||||
chr14:104103372
|
A | G | 12 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0028others(9): Show | 18 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.641-191A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103372 | ||||||
chr14:104103376
|
C | T | 1 | a0003c0004t0003g0092 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.641-187C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103376 | ||||||
chr14:104103385
|
C | A | 1 | a0003c0004t0003g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.641-178C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103385 | ||||||
chr14:104103464
|
C | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(136): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.641-99C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103464 | ||||||
chr14:104103541
|
A | G | 1 | a0002c0002t0002g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.641-22A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103541 | ||||||
chr14:104103685
|
G | A | 1 | a0002c0003t0001g0196 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.753+10G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103685 | ||||||
chr14:104103685
|
G | C | 1 | a0010c0015t0002g0235 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.753+10G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103685 | ||||||
chr14:104103739
|
G | A | 1 | a0003c0004t0003g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.753+64G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103739 | ||||||
chr14:104103751
|
C | T | 8 | a0001c0001t0011g0244a0001c0001t0025g0243a0001c0024t0011g0060others(5): Show | 8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.753+76C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103751 | ||||||
chr14:104103779
|
C | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(107): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.753+104C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103779 | ||||||
chr14:104103782
|
C | T | 1 | a0001c0001t0024g0037 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.753+107C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103782 | ||||||
chr14:104103914
|
C | T | 1 | a0001c0007t0008g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.753+239C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103914 | ||||||
chr14:104104075
|
C | A | 14 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0028others(11): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.754-229C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104104075 | ||||||
chr14:104104115
|
G | C | 1 | a0002c0002t0013g0197 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.754-189G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104104115 | ||||||
chr14:104104178
|
G | A | 1 | a0001c0001t0024g0037 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.754-126G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104104178 | ||||||
chr14:104104292
|
A | C | 7 | a0002c0003t0006g0049a0002c0003t0006g0050a0002c0003t0006g0051others(4): Show | 10 | HG00735.hp1 HG01099.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.754-12A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104104292 | ||||||
chr14:104104534
|
G | A | 1 | a0002c0005t0002g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.936+48G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 8/15 | chr14 | 104104534 | ||||||
chr14:104104557
|
C | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0127a0001c0001t0036g0015 | 4 | HG00423.hp1 HG02165.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-65C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 8/15 | chr14 | 104104557 | ||||||
chr14:104104567
|
T | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(253): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.937-55T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 8/15 | chr14 | 104104567 | ||||||
chr14:104104925
|
C | G | 1 | a0001c0001t0001g0130 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1050+190C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 9/15 | chr14 | 104104925 | ||||||
chr14:104105102
|
C | T | 14 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0028others(11): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1051-226C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 9/15 | chr14 | 104105102 | ||||||
chr14:104105161
|
C | T | 1 | a0002c0002t0002g0218 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1051-167C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 9/15 | chr14 | 104105161 | ||||||
chr14:104105184
|
C | G | 1 | a0002c0002t0002g0195 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1051-144C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 9/15 | chr14 | 104105184 | ||||||
chr14:104105257
|
G | A | 1 | a0001c0001t0005g0023 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1051-71G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 9/15 | chr14 | 104105257 | ||||||
chr14:104105457
|
G | C | 2 | a0002c0002t0002g0172a0002c0002t0002g0173 | 2 | HG02451.hp1 HG02647.hp2 |
splice_region_variant&intron_variant | LOW | c.1173+7G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105457 | ||||||
chr14:104105483
|
C | G | 38 | a0002c0002t0019g0174a0003c0004t0003g0003a0003c0004t0003g0007others(35): Show | 54 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1173+33C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105483 | ||||||
chr14:104105489
|
A | C | 1 | a0003c0004t0003g0092 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1173+39A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105489 | ||||||
chr14:104105489
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(252): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1173+39A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105489 | ||||||
chr14:104105536
|
C | T | 1 | a0002c0002t0002g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1173+86C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105536 | ||||||
chr14:104105577
|
C | T | 1 | a0002c0002t0002g0205 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1173+127C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105577 | ||||||
chr14:104105766
|
G | A | 4 | a0001c0024t0011g0060a0002c0003t0017g0171a0002c0003t0038g0165others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+316G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105766 | ||||||
chr14:104105824
|
G | A | 1 | a0001c0001t0004g0066 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1173+374G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105824 | ||||||
chr14:104105989
|
C | T | 1 | a0001c0001t0001g0036 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1173+539C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105989 | ||||||
chr14:104106067
|
A | T | 1 | a0001c0006t0028g0143 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1173+617A>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104106067 | ||||||
chr14:104106297
|
G | A | 1 | a0002c0002t0002g0206 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1174-502G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104106297 | ||||||
chr14:104106330
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(105): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1174-469G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104106330 | ||||||
chr14:104106352
|
C | T | 14 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0028others(11): Show | 22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1174-447C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104106352 | ||||||
chr14:104106564
|
G | A | 1 | a0002c0002t0002g0009 | 4 | HG01192.hp1 HG01975.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174-235G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104106564 | ||||||
chr14:104106932
|
C | T | 5 | a0001c0024t0011g0060a0002c0003t0017g0162a0002c0003t0017g0171others(2): Show | 5 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1269+38C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 11/15 | chr14 | 104106932 | ||||||
chr14:104107353
|
A | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(253): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
splice_region_variant&intron_variant | LOW | c.1433+8A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104107353 | ||||||
chr14:104107479
|
C | T | 1 | a0001c0001t0001g0036 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1433+134C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104107479 | ||||||
chr14:104107556
|
C | T | 1 | a0002c0003t0006g0051 | 2 | HG01099.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1433+211C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104107556 | ||||||
chr14:104107696
|
C | A | 1 | a0002c0003t0005g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1433+351C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104107696 | ||||||
chr14:104107855
|
C | T | 1 | a0002c0003t0010g0238 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1433+510C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104107855 | ||||||
chr14:104107856
|
G | A | 1 | a0002c0002t0013g0198 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1433+511G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104107856 | ||||||
chr14:104108016
|
C | T | 3 | a0001c0006t0002g0033a0002c0003t0002g0178a0002c0010t0002g0046 | 5 | HG02280.hp2 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1433+671C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108016 | ||||||
chr14:104108108
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1433+763C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108108 | ||||||
chr14:104108194
|
C | T | 2 | a0001c0019t0010g0245a0002c0013t0039g0168 | 2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1433+849C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108194 | ||||||
chr14:104108241
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1433+896G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108241 | ||||||
chr14:104108424
|
C | T | 1 | a0003c0004t0003g0089 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1434-805C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108424 | ||||||
chr14:104108439
|
G | A | 6 | a0001c0007t0002g0248a0001c0007t0008g0067a0001c0007t0008g0079others(3): Show | 7 | HG02615.hp2 HG02976.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1434-790G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108439 | ||||||
chr14:104108603
|
A | G | 2 | a0001c0001t0001g0147a0002c0003t0001g0210 | 2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1434-626A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108603 | ||||||
chr14:104108728
|
C | A | 1 | a0002c0002t0019g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1434-501C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108728 | ||||||
chr14:104108793
|
C | T | 35 | a0002c0002t0019g0174a0003c0004t0003g0003a0003c0004t0003g0007others(32): Show | 50 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1434-436C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108793 | ||||||
chr14:104108873
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(89): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1434-356C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108873 | ||||||
chr14:104108953
|
C | G | 35 | a0003c0004t0003g0003a0003c0004t0003g0007a0003c0004t0003g0012others(32): Show | 51 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1434-276C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108953 | ||||||
chr14:104108989
|
C | A | 35 | a0003c0004t0003g0003a0003c0004t0003g0007a0003c0004t0003g0012others(32): Show | 51 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1434-240C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108989 | ||||||
chr14:104109000
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1434-229C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104109000 | ||||||
chr14:104109122
|
C | G | 1 | a0003c0004t0003g0064 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1434-107C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104109122 | ||||||
chr14:104109129
|
C | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(250): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1434-100C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104109129 | ||||||
chr14:104109194
|
C | G | 91 | a0001c0001t0001g0105a0001c0001t0001g0117a0001c0001t0001g0121others(88): Show | 139 | HG00558.hp2 HG00639.hp1 HG00673.hp2 others(136): Show |
intron_variant | MODIFIER | c.1434-35C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104109194 | ||||||
chr14:104109343
|
C | T | 1 | a0002c0003t0038g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1520+28C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109343 | ||||||
chr14:104109532
|
G | A | 76 | a0001c0001t0002g0110a0001c0001t0004g0013a0001c0001t0004g0024others(73): Show | 112 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.1520+217G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109532 | ||||||
chr14:104109597
|
CAT | C | 65 | a0001c0001t0002g0110a0001c0006t0002g0033a0001c0006t0002g0125others(62): Show | 103 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(100): Show |
intron_variant | MODIFIER | c.1520+283_1520+284d others(4): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109597 | ||||||
chr14:104109601
|
T | C | 8 | a0001c0001t0011g0244a0001c0001t0025g0243a0001c0024t0011g0060others(5): Show | 8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1520+286T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109601 | ||||||
chr14:104109668
|
G | T | 1 | a0001c0007t0008g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1520+353G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109668 | ||||||
chr14:104109888
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1520+573G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109888 | ||||||
chr14:104109897
|
A | G | 3 | a0002c0003t0009g0179a0002c0003t0009g0182a0002c0003t0009g0183 | 3 | HG00280.hp2 HG00642.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1520+582A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109897 | ||||||
chr14:104110111
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(96): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1520+796G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110111 | ||||||
chr14:104110128
|
G | A | 1 | a0002c0002t0002g0048 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1520+813G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110128 | ||||||
chr14:104110131
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1520+816T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110131 | ||||||
chr14:104110326
|
C | T | 1 | a0001c0001t0001g0027 | 2 | HG01516.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1520+1011C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110326 | ||||||
chr14:104110410
|
C | G | 1 | a0003c0004t0003g0155 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1521-1092C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110410 | ||||||
chr14:104110479
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(132): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1521-1023A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110479 | ||||||
chr14:104110547
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1521-955C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110547 | ||||||
chr14:104110607
|
G | C | 1 | a0005c0021t0003g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1521-895G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110607 | ||||||
chr14:104110658
|
C | T | 1 | a0002c0003t0037g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1521-844C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110658 | ||||||
chr14:104110670
|
T | C | 2 | a0002c0002t0002g0202a0002c0002t0002g0203 | 2 | HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1521-832T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110670 | ||||||
chr14:104110794
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(132): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1521-708G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110794 | ||||||
chr14:104110796
|
G | A | 66 | a0001c0001t0002g0110a0001c0006t0002g0033a0001c0006t0002g0125others(63): Show | 104 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(101): Show |
intron_variant | MODIFIER | c.1521-706G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110796 | ||||||
chr14:104110858
|
C | T | 1 | a0003c0004t0003g0029 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1521-644C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110858 | ||||||
chr14:104111056
|
C | T | 1 | a0003c0004t0003g0097 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1521-446C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111056 | ||||||
chr14:104111062
|
G | A | 2 | a0001c0001t0007g0025a0001c0001t0007g0078 | 3 | HG01891.hp1 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1521-440G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111062 | ||||||
chr14:104111192
|
G | A | 1 | a0001c0001t0007g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1521-310G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111192 | ||||||
chr14:104111223
|
ATGTATGC others(5): Show |
A | 1 | a0002c0016t0006g0212 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1521-263_1521-252d others(14): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 104111223 | |||||
chr14:104111237
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1521-265G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111237 | ||||||
chr14:104111279
|
A | G | 1 | a0003c0004t0003g0251 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1521-223A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111279 | ||||||
chr14:104111288
|
C | T | 2 | a0011c0011t0023g0154a0012c0012t0023g0237 | 2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1521-214C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111288 | ||||||
chr14:104111311
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0085 | 2 | HG01257.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1521-191A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111311 | ||||||
chr14:104111378
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1521-124T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111378 | ||||||
chr14:104111480
|
C | T | 4 | a0001c0007t0008g0067a0001c0007t0008g0079a0001c0007t0008g0080others(1): Show | 4 | HG02976.hp2 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521-22C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111480 | ||||||
chr14:104111489
|
C | T | 4 | a0001c0007t0008g0067a0001c0007t0008g0079a0001c0007t0008g0080others(1): Show | 4 | HG02976.hp2 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521-13C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111489 | ||||||
chr14:104111740
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1620+139C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 14/15 | chr14 | 104111740 | ||||||
chr14:104111741
|
G | A | 1 | a0004c0008t0004g0021 | 3 | HG00639.hp1 HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1620+140G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 14/15 | chr14 | 104111741 | ||||||
chr14:104112091
|
A | G | 4 | a0002c0002t0002g0053a0002c0002t0013g0188a0002c0002t0013g0197others(1): Show | 5 | HG02132.hp1 NA18944.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1701+91A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 15/15 | chr14 | 104112091 | ||||||
chr14:104112144
|
C | T | 8 | a0001c0001t0011g0244a0001c0001t0025g0243a0001c0024t0011g0060others(5): Show | 8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1701+144C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 15/15 | chr14 | 104112144 | ||||||
chr14:104112345
|
A | T | 2 | a0011c0011t0023g0154a0012c0012t0023g0237 | 2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1702-179A>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 15/15 | chr14 | 104112345 | ||||||
chr14:104112480
|
G | A | 13 | a0001c0001t0004g0013a0001c0001t0004g0024a0001c0001t0004g0028others(10): Show | 20 | HG00639.hp1 HG01071.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1702-44G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 15/15 | chr14 | 104112480 |