geneid | 2252 |
---|---|
ensemblid | ENSG00000140285.12 |
hgncid | 3685 |
symbol | FGF7 |
name | fibroblast growth factor 7 |
refseq_nuc | NM_002009.4 |
refseq_prot | NP_002000.1 |
ensembl_nuc | ENST00000267843.9 |
ensembl_prot | ENSP00000267843.4 |
mane_status | MANE Select |
chr | chr15 |
start | 49423242 |
end | 49488775 |
strand | + |
ver | v1.2 |
region | chr15:49423242-49488775 |
region5000 | chr15:49418242-49493775 |
regionname0 | FGF7_chr15_49423242_49488775 |
regionname5000 | FGF7_chr15_49418242_49493775 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 194 | 358 | 86 | 54 | 152 | 14 | 50 | 122 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 585 | 358 | 86 | 54 | 152 | 14 | 50 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 4737 | 81 | 34 | 11 | 26 | 4 | 5 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0002 | 0/0 | 4733 | 72 | 2 | 17 | 39 | 2 | 12 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0003 | 0/0 | 4737 | 38 | 1 | 2 | 33 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0004 | 0/1 | 4737 | 30 | 3 | 10 | 2 | 4 | 10 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0005 | 0/0 | 4737 | 23 | 1 | 6 | 15 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0006 | 0/0 | 4737 | 21 | 0 | 1 | 15 | 0 | 5 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0007 | 0/0 | 4734 | 15 | 13 | 1 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0008 | 0/0 | 4737 | 13 | 0 | 1 | 9 | 0 | 3 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0009 | 0/0 | 4737 | 11 | 11 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0010 | 0/0 | 4737 | 10 | 1 | 1 | 2 | 1 | 5 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0011 | 0/0 | 4734 | 7 | 1 | 0 | 6 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0012 | 0/0 | 4737 | 5 | 4 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0013 | 0/0 | 4739 | 4 | 4 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0014 | 0/0 | 4737 | 4 | 4 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0015 | 0/0 | 4737 | 4 | 4 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0016 | 0/0 | 4734 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0017 | 0/0 | 4737 | 3 | 0 | 1 | 0 | 1 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0018 | 0/0 | 4737 | 2 | 0 | 1 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0019 | 0/0 | 4737 | 2 | 0 | 0 | 0 | 2 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0020 | 0/0 | 4736 | 2 | 0 | 0 | 0 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0021 | 0/0 | 4733 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0022 | 0/0 | 4733 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0023 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0024 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0025 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0026 | 0/0 | 4737 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0027 | 0/0 | 4733 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
t0028 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0003 | 0/0 | 5 | 1 | 2 | 1 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0005 | 0/0 | 4 | 1 | 0 | 2 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0006 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0007 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0030 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 585 | 358 | 86 | 54 | 152 | 14 | 50 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5321 | 81 | 34 | 11 | 26 | 4 | 5 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0002 | 0/0 | 5317 | 72 | 2 | 17 | 39 | 2 | 12 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0003 | 0/0 | 5321 | 38 | 1 | 2 | 33 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0004 | 0/1 | 5321 | 30 | 3 | 10 | 2 | 4 | 10 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0005 | 0/0 | 5321 | 23 | 1 | 6 | 15 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0006 | 0/0 | 5321 | 21 | 0 | 1 | 15 | 0 | 5 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0007 | 0/0 | 5318 | 15 | 13 | 1 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0008 | 0/0 | 5321 | 13 | 0 | 1 | 9 | 0 | 3 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0009 | 0/0 | 5321 | 11 | 11 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0010 | 0/0 | 5321 | 10 | 1 | 1 | 2 | 1 | 5 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0011 | 0/0 | 5318 | 7 | 1 | 0 | 6 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0012 | 0/0 | 5321 | 5 | 4 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0013 | 0/0 | 5323 | 4 | 4 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0014 | 0/0 | 5321 | 4 | 4 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0015 | 0/0 | 5321 | 4 | 4 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0016 | 0/0 | 5318 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0017 | 0/0 | 5321 | 3 | 0 | 1 | 0 | 1 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0018 | 0/0 | 5321 | 2 | 0 | 1 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0019 | 0/0 | 5321 | 2 | 0 | 0 | 0 | 2 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0020 | 0/0 | 5320 | 2 | 0 | 0 | 0 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0021 | 0/0 | 5317 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0022 | 0/0 | 5317 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0023 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0024 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0025 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0026 | 0/0 | 5321 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0027 | 0/0 | 5317 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
a0001c0001t0028 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | copy fasta | chr15 | 49418242 | 49493775 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 1 | 1 | 1 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0005 | 0/0 | 4 | 1 | 0 | 2 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0030 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0006 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0007 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0008g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0008g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0008g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0008g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0008g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0008g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0008g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0008g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0008g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0008g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0008g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0009g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0010g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0010g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0010g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0010g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0010g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0010g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0010g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0010g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0010g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0010g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0011g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0011g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0011g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0011g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0011g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0012g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0012g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0012g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0012g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0013g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0013g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0013g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0014g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0014g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0014g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0014g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0015g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0015g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0015g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0015g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0016g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0016g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0016g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0017g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0017g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0017g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0018g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0018g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0019g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0020g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0020g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0021g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0022g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0023g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0024g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0025g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0026g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0027g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
a0001c0001t0028g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0007 | EUR | GBR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0251 | EUR | GBR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0007 | EUR | FIN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0239 | EUR | FIN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | FIN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00408 | hp1 | a0001 | c0001 | t0010 | g0282 | EAS | CHS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | CHS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00558 | hp1 | a0001 | c0001 | t0016 | g0057 | EAS | CHS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00558 | hp2 | a0001 | c0001 | t0008 | g0289 | EAS | CHS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00609 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | CHS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00642 | hp1 | a0001 | c0001 | t0008 | g0276 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0093 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0272 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00735 | hp2 | a0001 | c0001 | t0018 | g0072 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0075 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0016 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01081 | hp1 | a0001 | c0001 | t0005 | g0271 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0091 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01169 | hp1 | a0001 | c0001 | t0007 | g0232 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0078 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01192 | hp2 | a0001 | c0001 | t0017 | g0003 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01255 | hp1 | a0001 | c0001 | t0012 | g0018 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01255 | hp2 | a0001 | c0001 | t0010 | g0286 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01257 | hp1 | a0001 | c0001 | t0021 | g0253 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0193 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0079 | EUR | IBS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01516 | hp2 | a0001 | c0001 | t0019 | g0022 | EUR | IBS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01517 | hp1 | a0001 | c0001 | t0017 | g0148 | EUR | IBS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01517 | hp2 | a0001 | c0001 | t0019 | g0022 | EUR | IBS | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0049 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01884 | hp2 | a0001 | c0001 | t0014 | g0064 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0061 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0195 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02040 | hp2 | a0001 | c0001 | t0008 | g0040 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02055 | hp1 | a0001 | c0001 | t0012 | g0068 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0045 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02074 | hp2 | a0001 | c0001 | t0028 | g0280 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02083 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02135 | hp1 | a0001 | c0001 | t0008 | g0041 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0233 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02145 | hp2 | a0001 | c0001 | t0024 | g0121 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | CDX | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02258 | hp2 | a0001 | c0001 | t0014 | g0070 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02273 | hp2 | a0001 | c0001 | t0006 | g0124 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0083 | AMR | PEL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02451 | hp1 | a0001 | c0001 | t0014 | g0090 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0184 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0042 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0082 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02602 | hp2 | a0001 | c0001 | t0006 | g0132 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0198 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02622 | hp2 | a0001 | c0001 | t0015 | g0187 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0270 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02683 | hp1 | a0001 | c0001 | t0027 | g0224 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0074 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02698 | hp2 | a0001 | c0001 | t0020 | g0275 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02717 | hp1 | a0001 | c0001 | t0015 | g0214 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0050 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0081 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02735 | hp2 | a0001 | c0001 | t0010 | g0287 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02738 | hp1 | a0001 | c0001 | t0010 | g0293 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02738 | hp2 | a0001 | c0001 | t0020 | g0274 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02818 | hp2 | a0001 | c0001 | t0009 | g0052 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02886 | hp1 | a0001 | c0001 | t0013 | g0089 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02895 | hp2 | a0001 | c0001 | t0025 | g0135 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02965 | hp2 | a0001 | c0001 | t0012 | g0018 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0255 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03017 | hp1 | a0001 | c0001 | t0008 | g0273 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0261 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03041 | hp2 | a0001 | c0001 | t0014 | g0120 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0048 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0182 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03130 | hp2 | a0001 | c0001 | t0013 | g0065 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03139 | hp2 | a0001 | c0001 | t0015 | g0188 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03195 | hp1 | a0001 | c0001 | t0010 | g0283 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03209 | hp1 | a0001 | c0001 | t0009 | g0051 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03239 | hp1 | a0001 | c0001 | t0018 | g0164 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03453 | hp1 | a0001 | c0001 | t0007 | g0178 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0125 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0179 | AFR | ESN | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03540 | hp2 | a0001 | c0001 | t0012 | g0071 | AFR | GWD | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0229 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0047 | AFR | MSL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0026 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0077 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03688 | hp2 | a0001 | c0001 | t0010 | g0288 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03704 | hp1 | a0001 | c0001 | t0008 | g0291 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03704 | hp2 | a0001 | c0001 | t0017 | g0145 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0086 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03831 | hp2 | a0001 | c0001 | t0010 | g0294 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0073 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0123 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0107 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG04115 | hp1 | a0001 | c0001 | t0026 | g0111 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG04184 | hp2 | a0001 | c0001 | t0008 | g0290 | SAS | BEB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0080 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0053 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0026 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG04228 | hp2 | a0001 | c0001 | t0010 | g0285 | SAS | STU | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18522 | hp1 | a0001 | c0001 | t0013 | g0067 | AFR | YRI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | CHB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18612 | hp2 | a0001 | c0001 | t0006 | g0122 | EAS | CHB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18747 | hp1 | a0001 | c0001 | t0008 | g0041 | EAS | CHB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0027 | EAS | CHB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0234 | AFR | YRI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18942 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18946 | hp1 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18947 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18949 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18951 | hp2 | a0001 | c0001 | t0008 | g0292 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18952 | hp2 | a0001 | c0001 | t0016 | g0060 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18957 | hp1 | a0001 | c0001 | t0011 | g0014 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18957 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18961 | hp2 | a0001 | c0001 | t0011 | g0216 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18966 | hp2 | a0001 | c0001 | t0008 | g0040 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18972 | hp1 | a0001 | c0001 | t0006 | g0199 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18975 | hp2 | a0001 | c0001 | t0011 | g0014 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18977 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18979 | hp1 | a0001 | c0001 | t0022 | g0035 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18989 | hp1 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0063 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18990 | hp2 | a0001 | c0001 | t0008 | g0279 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18999 | hp2 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19001 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19004 | hp1 | a0001 | c0001 | t0008 | g0278 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19005 | hp2 | a0001 | c0001 | t0011 | g0230 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19006 | hp2 | a0001 | c0001 | t0006 | g0136 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0203 | AFR | LWK | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19058 | hp2 | a0001 | c0001 | t0008 | g0277 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19059 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19059 | hp2 | a0001 | c0001 | t0006 | g0114 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19064 | hp2 | a0001 | c0001 | t0011 | g0201 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19070 | hp1 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19074 | hp1 | a0001 | c0001 | t0016 | g0055 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19077 | hp2 | a0001 | c0001 | t0006 | g0027 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19079 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19087 | hp1 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19088 | hp1 | a0001 | c0001 | t0011 | g0014 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19088 | hp2 | a0001 | c0001 | t0010 | g0281 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19089 | hp1 | a0001 | c0001 | t0006 | g0113 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19240 | hp1 | a0001 | c0001 | t0013 | g0066 | AFR | YRI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ASW | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA20129 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | ASW | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | TSI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA20805 | hp1 | a0001 | c0001 | t0010 | g0284 | EUR | TSI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA20905 | hp1 | a0001 | c0001 | t0007 | g0133 | SAS | GIH | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0105 | SAS | GIH | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02109 | hp1 | a0001 | c0001 | t0011 | g0220 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG02486 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | ACB | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG06807 | hp1 | a0001 | c0001 | t0015 | g0186 | AFR | USA | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
HG06807 | hp2 | a0001 | c0001 | t0012 | g0069 | AFR | USA | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA20300 | hp1 | a0001 | c0001 | t0009 | g0043 | AFR | USA | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | USA | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
NA21309 | hp2 | a0001 | c0001 | t0023 | g0095 | AFR | LWK | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0006 | REF | REF | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0030 | REF | REF | FGF7_chr15_49418242_49493775 | FGF7 | chr15 | 49418242 | 49493775 |
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 |
---|
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:49424044
|
A | C | 4 | a0001c0001t0008a0001c0001t0010a0001c0001t0020others(1): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-254A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/4 | 254 | chr15 | 49424044 | |||||
chr15:49424080
|
T | C | 1 | a0001c0001t0021 | 1 | HG01257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-218T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/4 | 218 | chr15 | 49424080 | |||||
chr15:49424281
|
C | T | 1 | a0001c0001t0017 | 3 | HG01192.hp2 HG01517.hp1 HG03704.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-17C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/4 | chr15 | 49424281 | ||||||
chr15:49484687
|
A | G | 1 | a0001c0001t0027 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 183 | chr15 | 49484687 | |||||
chr15:49484760
|
C | A | 10 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(7): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*256C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 256 | chr15 | 49484760 | |||||
chr15:49484856
|
C | T | 6 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(3): Show | 79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*352C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 352 | chr15 | 49484856 | |||||
chr15:49484929
|
A | G | 10 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(7): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*425A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 425 | chr15 | 49484929 | |||||
chr15:49485234
|
T | TAC | 1 | a0001c0001t0013 | 4 | HG02886.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*731_*732dupAC | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 733 | INFO_REALIGN_3_PRIME | chr15 | 49485234 | ||||
chr15:49485271
|
A | T | 11 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(8): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*767A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 767 | chr15 | 49485271 | |||||
chr15:49485473
|
TA | T | 5 | a0001c0001t0002a0001c0001t0020a0001c0001t0021others(2): Show | 77 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*979delA | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 979 | INFO_REALIGN_3_PRIME | chr15 | 49485473 | ||||
chr15:49485703
|
C | T | 5 | a0001c0001t0002a0001c0001t0011a0001c0001t0021others(2): Show | 82 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1199C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 1199 | chr15 | 49485703 | |||||
chr15:49485860
|
C | T | 1 | a0001c0001t0015 | 4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1356C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 1356 | chr15 | 49485860 | |||||
chr15:49486182
|
T | C | 1 | a0001c0001t0012 | 5 | HG01255.hp1 HG02055.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1678T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 1678 | chr15 | 49486182 | |||||
chr15:49486225
|
C | T | 1 | a0001c0001t0026 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1721C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 1721 | chr15 | 49486225 | |||||
chr15:49486424
|
T | C | 1 | a0001c0001t0018 | 2 | HG00735.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1920T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 1920 | chr15 | 49486424 | |||||
chr15:49486625
|
T | A | 1 | a0001c0001t0023 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2121T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 2121 | chr15 | 49486625 | |||||
chr15:49486937
|
A | G | 1 | a0001c0001t0019 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2433A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 2433 | chr15 | 49486937 | |||||
chr15:49487038
|
T | A | 6 | a0001c0001t0002a0001c0001t0007a0001c0001t0011others(3): Show | 97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2534T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 2534 | chr15 | 49487038 | |||||
chr15:49487079
|
T | C | 10 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(7): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2575T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 2575 | chr15 | 49487079 | |||||
chr15:49487420
|
AATT | A | 6 | a0001c0001t0002a0001c0001t0007a0001c0001t0011others(3): Show | 97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2919_*2921delTAT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 2919 | INFO_REALIGN_3_PRIME | chr15 | 49487420 | ||||
chr15:49487591
|
C | T | 2 | a0001c0001t0004a0001c0001t0018 | 32 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3087C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3087 | chr15 | 49487591 | |||||
chr15:49487647
|
T | G | 1 | a0001c0001t0020 | 2 | HG02698.hp2 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3143T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3143 | chr15 | 49487647 | |||||
chr15:49487706
|
A | G | 1 | a0001c0001t0022 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3202A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3202 | chr15 | 49487706 | |||||
chr15:49487737
|
C | T | 1 | a0001c0001t0006 | 21 | HG02273.hp2 HG02602.hp2 HG03491.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3233C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3233 | chr15 | 49487737 | |||||
chr15:49487805
|
C | A | 3 | a0001c0001t0005a0001c0001t0008a0001c0001t0016 | 39 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3301C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3301 | chr15 | 49487805 | |||||
chr15:49488162
|
T | C | 1 | a0001c0001t0024 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3658T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3658 | chr15 | 49488162 | |||||
chr15:49488165
|
G | A | 6 | a0001c0001t0002a0001c0001t0007a0001c0001t0011others(3): Show | 97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*3661G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3661 | chr15 | 49488165 | |||||
chr15:49488183
|
G | C | 1 | a0001c0001t0025 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3679G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 3679 | chr15 | 49488183 | |||||
chr15:49488543
|
T | C | 3 | a0001c0001t0012a0001c0001t0013a0001c0001t0014 | 13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4039T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 4039 | chr15 | 49488543 | |||||
chr15:49488598
|
TATC | T | 1 | a0001c0001t0016 | 3 | HG00558.hp1 NA18952.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4097_*4099delCAT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 4097 | INFO_REALIGN_3_PRIME | chr15 | 49488598 | ||||
chr15:49488624
|
A | C | 12 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(9): Show | 127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*4120A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 4120 | chr15 | 49488624 | |||||
chr15:49488633
|
T | C | 2 | a0001c0001t0015a0001c0001t0020 | 6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4129T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 4/4 | 4129 | chr15 | 49488633 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:49423558
|
A | ACTAT | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-267+119_-267+122d others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | 49423558 | |||||
chr15:49423728
|
A | G | 3 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272 | 3 | HG00733.hp2 HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-267+288A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 1/3 | chr15 | 49423728 | ||||||
chr15:49423810
|
A | G | 85 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(82): Show | 103 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.-266-222A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 1/3 | chr15 | 49423810 | ||||||
chr15:49423820
|
TG | T | 4 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(1): Show | 4 | HG01175.hp1 HG01358.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-266-211delG | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 1/3 | chr15 | 49423820 | ||||||
chr15:49423896
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-266-136G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 1/3 | chr15 | 49423896 | ||||||
chr15:49423944
|
C | T | 2 | a0001c0001t0006g0033a0001c0001t0006g0191 | 3 | NA18942.hp2 NA18946.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-266-88C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 1/3 | chr15 | 49423944 | ||||||
chr15:49424648
|
T | C | 175 | a0001c0001t0001g0054a0001c0001t0001g0192a0001c0001t0002g0001others(172): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.286+65T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49424648 | ||||||
chr15:49424822
|
T | C | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+239T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49424822 | ||||||
chr15:49425048
|
A | T | 1 | a0001c0001t0001g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.286+465A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425048 | ||||||
chr15:49425089
|
G | A | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+506G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425089 | ||||||
chr15:49425302
|
T | C | 5 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG01109.hp2 HG02922.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+719T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425302 | ||||||
chr15:49425313
|
A | G | 1 | a0001c0001t0004g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.286+730A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425313 | ||||||
chr15:49425395
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.286+812G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425395 | ||||||
chr15:49425451
|
G | A | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+868G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425451 | ||||||
chr15:49425501
|
C | A | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+918C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425501 | ||||||
chr15:49425692
|
A | G | 1 | a0001c0001t0005g0092 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.286+1109A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49425692 | ||||||
chr15:49426009
|
A | C | 1 | a0001c0001t0005g0091 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.286+1426A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426009 | ||||||
chr15:49426051
|
A | T | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+1468A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426051 | ||||||
chr15:49426065
|
GGATAATA others(3): Show |
G | 5 | a0001c0001t0008g0040a0001c0001t0008g0276a0001c0001t0008g0277others(2): Show | 6 | HG00642.hp1 HG02040.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.286+1483_286+1492d others(12): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426065 | ||||||
chr15:49426151
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+1568C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426151 | ||||||
chr15:49426260
|
G | A | 268 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(265): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.286+1677G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426260 | ||||||
chr15:49426322
|
C | T | 26 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(23): Show | 28 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.286+1739C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426322 | ||||||
chr15:49426381
|
G | T | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+1798G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426381 | ||||||
chr15:49426531
|
G | T | 36 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(33): Show | 41 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.286+1948G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426531 | ||||||
chr15:49426682
|
T | C | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+2099T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426682 | ||||||
chr15:49426739
|
C | T | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+2156C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426739 | ||||||
chr15:49426799
|
A | G | 1 | a0001c0001t0002g0264 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.286+2216A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49426799 | ||||||
chr15:49427214
|
A | G | 2 | a0001c0001t0014g0064a0001c0001t0014g0090 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.286+2631A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427214 | ||||||
chr15:49427557
|
C | T | 1 | a0001c0001t0013g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.286+2974C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427557 | ||||||
chr15:49427558
|
A | C | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+2975A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427558 | ||||||
chr15:49427559
|
T | A | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+2976T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427559 | ||||||
chr15:49427597
|
C | A | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+3014C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427597 | ||||||
chr15:49427619
|
C | A | 2 | a0001c0001t0009g0042a0001c0001t0009g0043 | 2 | HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.286+3036C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427619 | ||||||
chr15:49427666
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.286+3083G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427666 | ||||||
chr15:49427756
|
A | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(40): Show | 54 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.286+3173A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427756 | ||||||
chr15:49427910
|
T | A | 1 | a0001c0001t0001g0138 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.286+3327T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427910 | ||||||
chr15:49427911
|
A | T | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+3328A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49427911 | ||||||
chr15:49428051
|
G | A | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+3468G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428051 | ||||||
chr15:49428224
|
C | G | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+3641C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428224 | ||||||
chr15:49428367
|
T | C | 3 | a0001c0001t0010g0281a0001c0001t0010g0282a0001c0001t0028g0280 | 3 | HG00408.hp1 HG02074.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.286+3784T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428367 | ||||||
chr15:49428542
|
T | G | 25 | a0001c0001t0002g0197a0001c0001t0003g0004a0001c0001t0003g0008others(22): Show | 33 | HG01516.hp2 HG01517.hp2 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.286+3959T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428542 | ||||||
chr15:49428570
|
C | G | 1 | a0001c0001t0004g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.286+3987C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428570 | ||||||
chr15:49428581
|
G | A | 43 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(40): Show | 54 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.286+3998G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428581 | ||||||
chr15:49428706
|
C | T | 1 | a0001c0001t0003g0269 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.286+4123C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428706 | ||||||
chr15:49428874
|
G | A | 1 | a0001c0001t0008g0276 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.286+4291G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49428874 | ||||||
chr15:49429017
|
G | GTC | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+4435_286+4436i others(4): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49429017 | |||||
chr15:49429207
|
A | G | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+4624A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49429207 | ||||||
chr15:49429477
|
TC | T | 2 | a0001c0001t0005g0015a0001c0001t0005g0092 | 3 | NA18949.hp2 NA19082.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.286+4895delC | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49429477 | ||||||
chr15:49429658
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+5075G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49429658 | ||||||
chr15:49429685
|
T | G | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+5102T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49429685 | ||||||
chr15:49429855
|
G | T | 2 | a0001c0001t0010g0293a0001c0001t0010g0294 | 2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.286+5272G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49429855 | ||||||
chr15:49429872
|
G | A | 1 | a0001c0001t0005g0053 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.286+5289G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49429872 | ||||||
chr15:49430267
|
G | C | 1 | a0001c0001t0028g0280 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.286+5684G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49430267 | ||||||
chr15:49430421
|
G | T | 1 | a0001c0001t0003g0263 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.286+5838G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49430421 | ||||||
chr15:49430495
|
G | A | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+5912G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49430495 | ||||||
chr15:49430915
|
G | T | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+6332G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49430915 | ||||||
chr15:49431062
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.286+6479T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431062 | ||||||
chr15:49431097
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.286+6514A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431097 | ||||||
chr15:49431221
|
G | T | 3 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188 | 3 | HG02622.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.286+6638G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431221 | ||||||
chr15:49431224
|
G | A | 1 | a0001c0001t0009g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286+6641G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431224 | ||||||
chr15:49431258
|
G | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(40): Show | 54 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.286+6675G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431258 | ||||||
chr15:49431424
|
A | G | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+6841A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431424 | ||||||
chr15:49431552
|
C | T | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+6969C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431552 | ||||||
chr15:49431625
|
A | T | 1 | a0001c0001t0014g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.286+7042A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431625 | ||||||
chr15:49431630
|
T | C | 4 | a0001c0001t0013g0065a0001c0001t0013g0066a0001c0001t0013g0067others(1): Show | 4 | HG02886.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+7047T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431630 | ||||||
chr15:49431684
|
G | A | 25 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(22): Show | 33 | HG01516.hp2 HG01517.hp2 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.286+7101G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431684 | ||||||
chr15:49431701
|
C | G | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+7118C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431701 | ||||||
chr15:49431980
|
A | T | 1 | a0001c0001t0002g0262 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.286+7397A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431980 | ||||||
chr15:49431984
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0190 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.286+7401C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49431984 | ||||||
chr15:49432155
|
T | C | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+7572T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49432155 | ||||||
chr15:49432301
|
C | T | 1 | a0001c0001t0007g0261 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.286+7718C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49432301 | ||||||
chr15:49432390
|
C | T | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+7807C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49432390 | ||||||
chr15:49432564
|
C | G | 36 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(33): Show | 41 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.286+7981C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49432564 | ||||||
chr15:49432816
|
C | A | 1 | a0001c0001t0003g0100 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.286+8233C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49432816 | ||||||
chr15:49433008
|
G | A | 1 | a0001c0001t0013g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.286+8425G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433008 | ||||||
chr15:49433018
|
T | C | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+8435T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433018 | ||||||
chr15:49433025
|
A | G | 2 | a0001c0001t0003g0260a0001c0001t0003g0263 | 2 | NA18955.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.286+8442A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433025 | ||||||
chr15:49433069
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.286+8486T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433069 | ||||||
chr15:49433197
|
T | C | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.286+8614T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433197 | ||||||
chr15:49433371
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+8788C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433371 | ||||||
chr15:49433639
|
T | A | 5 | a0001c0001t0012g0018a0001c0001t0012g0068a0001c0001t0012g0069others(2): Show | 6 | HG01255.hp1 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.286+9056T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433639 | ||||||
chr15:49433643
|
G | C | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+9060G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433643 | ||||||
chr15:49433685
|
T | C | 1 | a0001c0001t0007g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.286+9102T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49433685 | ||||||
chr15:49434085
|
A | T | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.286+9502A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434085 | ||||||
chr15:49434135
|
C | T | 2 | a0001c0001t0002g0258a0001c0001t0002g0259 | 2 | NA18962.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.286+9552C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434135 | ||||||
chr15:49434170
|
G | A | 1 | a0001c0001t0006g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.286+9587G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434170 | ||||||
chr15:49434235
|
G | T | 268 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(265): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.286+9652G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434235 | ||||||
chr15:49434286
|
C | CT | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+9713dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49434286 | |||||
chr15:49434670
|
T | C | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+10087T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434670 | ||||||
chr15:49434723
|
T | A | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+10140T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434723 | ||||||
chr15:49434777
|
T | C | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0126others(21): Show | 32 | HG01243.hp1 HG02273.hp2 HG02602.hp2 others(29): Show |
intron_variant | MODIFIER | c.286+10194T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434777 | ||||||
chr15:49434820
|
G | A | 1 | a0001c0001t0003g0200 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.286+10237G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434820 | ||||||
chr15:49434852
|
ATAAT | A | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+10278_286+1028 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49434852 | |||||
chr15:49434879
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.286+10296A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49434879 | ||||||
chr15:49435031
|
A | G | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+10448A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435031 | ||||||
chr15:49435074
|
A | G | 291 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(288): Show | 352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.286+10491A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435074 | ||||||
chr15:49435243
|
G | A | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+10660G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435243 | ||||||
chr15:49435290
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+10707G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435290 | ||||||
chr15:49435358
|
TTAAGA | T | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+10781_286+1078 others(9): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49435358 | |||||
chr15:49435432
|
G | C | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+10849G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435432 | ||||||
chr15:49435724
|
G | T | 1 | a0001c0001t0005g0091 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.286+11141G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435724 | ||||||
chr15:49435809
|
C | T | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+11226C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49435809 | ||||||
chr15:49436305
|
A | G | 2 | a0001c0001t0002g0256a0001c0001t0002g0257 | 2 | HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.286+11722A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436305 | ||||||
chr15:49436354
|
A | G | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+11771A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436354 | ||||||
chr15:49436562
|
G | A | 60 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(57): Show | 67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.286+11979G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436562 | ||||||
chr15:49436592
|
A | G | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+12009A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436592 | ||||||
chr15:49436634
|
G | T | 26 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(23): Show | 30 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.286+12051G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436634 | ||||||
chr15:49436680
|
A | AT | 26 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(23): Show | 30 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.286+12099dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49436680 | |||||
chr15:49436684
|
A | C | 26 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(23): Show | 30 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.286+12101A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436684 | ||||||
chr15:49436685
|
G | T | 26 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(23): Show | 30 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.286+12102G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436685 | ||||||
chr15:49436689
|
C | A | 26 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(23): Show | 30 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.286+12106C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436689 | ||||||
chr15:49436731
|
G | A | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+12148G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436731 | ||||||
chr15:49436738
|
C | T | 1 | a0001c0001t0005g0053 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.286+12155C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436738 | ||||||
chr15:49436994
|
G | A | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+12411G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49436994 | ||||||
chr15:49437099
|
T | C | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+12516T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437099 | ||||||
chr15:49437168
|
T | C | 1 | a0001c0001t0003g0021 | 2 | NA19060.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.286+12585T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437168 | ||||||
chr15:49437728
|
G | A | 101 | a0001c0001t0001g0054a0001c0001t0002g0001a0001c0001t0002g0011others(98): Show | 126 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.286+13145G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437728 | ||||||
chr15:49437809
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.286+13226C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437809 | ||||||
chr15:49437890
|
A | T | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+13307A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437890 | ||||||
chr15:49437901
|
C | G | 1 | a0001c0001t0007g0255 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.286+13318C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437901 | ||||||
chr15:49437934
|
A | G | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+13351A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437934 | ||||||
chr15:49437959
|
A | C | 243 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.286+13376A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437959 | ||||||
chr15:49437960
|
G | A | 243 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.286+13377G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437960 | ||||||
chr15:49437998
|
G | A | 1 | a0001c0001t0009g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.286+13415G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49437998 | ||||||
chr15:49438008
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.286+13425G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438008 | ||||||
chr15:49438108
|
A | G | 1 | a0001c0001t0004g0020 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.286+13525A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438108 | ||||||
chr15:49438299
|
T | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0202a0001c0001t0011g0201 | 5 | HG02015.hp1 NA18980.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+13716T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438299 | ||||||
chr15:49438346
|
C | A | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+13763C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438346 | ||||||
chr15:49438399
|
C | G | 1 | a0001c0001t0003g0118 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.286+13816C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438399 | ||||||
chr15:49438453
|
T | A | 1 | a0001c0001t0007g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.286+13870T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438453 | ||||||
chr15:49438469
|
G | T | 1 | a0001c0001t0005g0063 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.286+13886G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438469 | ||||||
chr15:49438557
|
AAT | A | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+13976_286+1397 others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49438557 | |||||
chr15:49438587
|
T | C | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+14004T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438587 | ||||||
chr15:49438710
|
G | C | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+14127G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438710 | ||||||
chr15:49438717
|
C | A | 243 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.286+14134C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438717 | ||||||
chr15:49438820
|
T | C | 1 | a0001c0001t0014g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.286+14237T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438820 | ||||||
chr15:49438834
|
T | TGAGA | 174 | a0001c0001t0001g0054a0001c0001t0001g0192a0001c0001t0002g0001others(171): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.286+14259_286+1426 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49438834 | |||||
chr15:49438971
|
C | G | 1 | a0001c0001t0002g0254 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.286+14388C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49438971 | ||||||
chr15:49439101
|
G | C | 1 | a0001c0001t0002g0204 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.286+14518G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439101 | ||||||
chr15:49439137
|
A | G | 1 | a0001c0001t0007g0184 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.286+14554A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439137 | ||||||
chr15:49439158
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+14575T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439158 | ||||||
chr15:49439168
|
G | A | 1 | a0001c0001t0018g0072 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.286+14585G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439168 | ||||||
chr15:49439177
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+14594C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439177 | ||||||
chr15:49439271
|
G | C | 3 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0103 | 3 | NA18612.hp1 NA18971.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.286+14688G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439271 | ||||||
chr15:49439419
|
T | C | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+14836T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439419 | ||||||
chr15:49439453
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.286+14870T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439453 | ||||||
chr15:49439727
|
G | A | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+15144G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49439727 | ||||||
chr15:49440210
|
T | C | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+15627T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440210 | ||||||
chr15:49440217
|
T | C | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+15634T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440217 | ||||||
chr15:49440383
|
T | C | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+15800T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440383 | ||||||
chr15:49440512
|
T | A | 6 | a0001c0001t0012g0018a0001c0001t0012g0068a0001c0001t0012g0069others(3): Show | 7 | HG01255.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+15929T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440512 | ||||||
chr15:49440679
|
C | G | 1 | a0001c0001t0005g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.286+16096C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440679 | ||||||
chr15:49440845
|
A | G | 1 | a0001c0001t0021g0253 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.286+16262A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440845 | ||||||
chr15:49440861
|
T | A | 12 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.286+16278T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440861 | ||||||
chr15:49440876
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+16293T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440876 | ||||||
chr15:49440916
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.286+16333G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440916 | ||||||
chr15:49440961
|
A | T | 1 | a0001c0001t0002g0087 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.286+16378A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49440961 | ||||||
chr15:49441549
|
C | T | 60 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(57): Show | 67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.286+16966C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49441549 | ||||||
chr15:49441808
|
C | T | 1 | a0001c0001t0012g0071 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.286+17225C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49441808 | ||||||
chr15:49442067
|
T | C | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0126others(21): Show | 32 | HG01243.hp1 HG02273.hp2 HG02602.hp2 others(29): Show |
intron_variant | MODIFIER | c.286+17484T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442067 | ||||||
chr15:49442122
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.286+17539A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442122 | ||||||
chr15:49442127
|
T | A | 268 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(265): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.286+17544T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442127 | ||||||
chr15:49442301
|
G | A | 1 | a0001c0001t0002g0205 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.286+17718G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442301 | ||||||
chr15:49442346
|
C | T | 60 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(57): Show | 67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.286+17763C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442346 | ||||||
chr15:49442437
|
C | T | 161 | a0001c0001t0001g0054a0001c0001t0001g0192a0001c0001t0002g0001others(158): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.286+17854C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442437 | ||||||
chr15:49442494
|
G | A | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+17911G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442494 | ||||||
chr15:49442516
|
T | C | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+17933T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442516 | ||||||
chr15:49442538
|
T | C | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+17955T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442538 | ||||||
chr15:49442543
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.286+17960C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442543 | ||||||
chr15:49442646
|
A | G | 84 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(81): Show | 102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.286+18063A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442646 | ||||||
chr15:49442771
|
C | T | 17 | a0001c0001t0001g0054a0001c0001t0005g0002a0001c0001t0005g0015others(14): Show | 24 | HG00558.hp1 HG01070.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.286+18188C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442771 | ||||||
chr15:49442915
|
C | T | 200 | a0001c0001t0001g0054a0001c0001t0001g0119a0001c0001t0001g0192others(197): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.286+18332C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49442915 | ||||||
chr15:49443025
|
T | G | 1 | a0001c0001t0001g0170 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.286+18442T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443025 | ||||||
chr15:49443100
|
T | C | 61 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(58): Show | 70 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.286+18517T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443100 | ||||||
chr15:49443171
|
T | G | 1 | a0001c0001t0001g0142 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.286+18588T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443171 | ||||||
chr15:49443267
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+18684C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443267 | ||||||
chr15:49443282
|
A | G | 1 | a0001c0001t0007g0184 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.286+18699A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443282 | ||||||
chr15:49443409
|
C | T | 1 | a0001c0001t0003g0117 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.286+18826C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443409 | ||||||
chr15:49443468
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(39): Show | 51 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.286+18885C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443468 | ||||||
chr15:49443482
|
T | C | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+18899T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443482 | ||||||
chr15:49443532
|
C | CT | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+18951dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49443532 | |||||
chr15:49443542
|
A | T | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+18959A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443542 | ||||||
chr15:49443568
|
T | C | 2 | a0001c0001t0005g0270a0001c0001t0005g0271 | 2 | HG01081.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.286+18985T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443568 | ||||||
chr15:49443806
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.286+19223C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443806 | ||||||
chr15:49443924
|
TC | T | 101 | a0001c0001t0001g0054a0001c0001t0002g0001a0001c0001t0002g0011others(98): Show | 126 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.286+19342delC | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443924 | ||||||
chr15:49443992
|
G | A | 11 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0036others(8): Show | 14 | HG00408.hp2 HG01257.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+19409G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49443992 | ||||||
chr15:49444142
|
T | G | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+19559T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444142 | ||||||
chr15:49444222
|
T | G | 2 | a0001c0001t0002g0206a0001c0001t0021g0253 | 2 | HG01257.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.286+19639T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444222 | ||||||
chr15:49444228
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0014g0064 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.286+19645C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444228 | ||||||
chr15:49444367
|
G | C | 1 | a0001c0001t0002g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.286+19784G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444367 | ||||||
chr15:49444399
|
T | C | 1 | a0001c0001t0009g0045 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.286+19816T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444399 | ||||||
chr15:49444448
|
T | A | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+19865T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444448 | ||||||
chr15:49444554
|
T | C | 268 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(265): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.286+19971T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444554 | ||||||
chr15:49444621
|
G | A | 36 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(33): Show | 41 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.286+20038G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444621 | ||||||
chr15:49444709
|
G | T | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+20126G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49444709 | ||||||
chr15:49445068
|
A | G | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+20485A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445068 | ||||||
chr15:49445309
|
G | A | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+20726G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445309 | ||||||
chr15:49445337
|
G | T | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+20754G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445337 | ||||||
chr15:49445499
|
A | G | 243 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(240): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.286+20916A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445499 | ||||||
chr15:49445735
|
T | G | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+21152T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445735 | ||||||
chr15:49445860
|
G | A | 1 | a0001c0001t0005g0092 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.286+21277G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445860 | ||||||
chr15:49445961
|
T | C | 6 | a0001c0001t0012g0018a0001c0001t0012g0068a0001c0001t0012g0069others(3): Show | 7 | HG01255.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.286+21378T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49445961 | ||||||
chr15:49446036
|
T | C | 37 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(34): Show | 44 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.286+21453T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446036 | ||||||
chr15:49446099
|
T | A | 17 | a0001c0001t0001g0054a0001c0001t0005g0002a0001c0001t0005g0015others(14): Show | 24 | HG00558.hp1 HG01070.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.286+21516T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446099 | ||||||
chr15:49446117
|
T | C | 11 | a0001c0001t0010g0281a0001c0001t0010g0282a0001c0001t0010g0283others(8): Show | 11 | HG00408.hp1 HG01255.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+21534T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446117 | ||||||
chr15:49446137
|
G | T | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+21554G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446137 | ||||||
chr15:49446164
|
A | G | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+21581A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446164 | ||||||
chr15:49446173
|
C | T | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+21590C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446173 | ||||||
chr15:49446196
|
T | C | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.286+21613T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446196 | ||||||
chr15:49446270
|
T | C | 1 | a0001c0001t0002g0212 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.286+21687T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446270 | ||||||
chr15:49446331
|
C | T | 1 | a0001c0001t0014g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.286+21748C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446331 | ||||||
chr15:49446345
|
C | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(40): Show | 54 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.286+21762C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446345 | ||||||
chr15:49446492
|
G | C | 1 | a0001c0001t0008g0276 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.286+21909G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446492 | ||||||
chr15:49446585
|
AG | A | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+22005delG | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49446585 | |||||
chr15:49446792
|
A | C | 1 | a0001c0001t0001g0032 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.286+22209A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446792 | ||||||
chr15:49446850
|
T | C | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+22267T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446850 | ||||||
chr15:49446926
|
C | G | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+22343C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446926 | ||||||
chr15:49446928
|
G | A | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+22345G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49446928 | ||||||
chr15:49447147
|
A | C | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+22564A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447147 | ||||||
chr15:49447153
|
T | C | 273 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(270): Show | 332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.286+22570T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447153 | ||||||
chr15:49447271
|
A | G | 1 | a0001c0001t0001g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.286+22688A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447271 | ||||||
chr15:49447365
|
G | C | 1 | a0001c0001t0003g0117 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.286+22782G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447365 | ||||||
chr15:49447511
|
T | C | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+22928T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447511 | ||||||
chr15:49447521
|
T | C | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+22938T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447521 | ||||||
chr15:49447763
|
C | T | 1 | a0001c0001t0014g0120 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.286+23180C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447763 | ||||||
chr15:49447769
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+23186C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49447769 | ||||||
chr15:49448035
|
C | T | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+23452C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448035 | ||||||
chr15:49448107
|
A | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(40): Show | 54 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.286+23524A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448107 | ||||||
chr15:49448420
|
T | C | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+23837T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448420 | ||||||
chr15:49448674
|
C | CAT | 13 | a0001c0001t0008g0273a0001c0001t0012g0018a0001c0001t0012g0068others(10): Show | 14 | HG01255.hp1 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+24105_286+2410 others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49448674 | |||||
chr15:49448761
|
G | A | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+24178G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448761 | ||||||
chr15:49448866
|
G | A | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+24283G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448866 | ||||||
chr15:49448874
|
T | C | 37 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(34): Show | 44 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.286+24291T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448874 | ||||||
chr15:49448918
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+24335A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49448918 | ||||||
chr15:49449102
|
TCAAA | T | 84 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(81): Show | 102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.286+24522_286+2452 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49449102 | |||||
chr15:49449188
|
T | C | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+24605T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49449188 | ||||||
chr15:49449557
|
G | A | 1 | a0001c0001t0002g0213 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.286+24974G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49449557 | ||||||
chr15:49449580
|
T | A | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+24997T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49449580 | ||||||
chr15:49449651
|
G | C | 1 | a0001c0001t0001g0143 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.286+25068G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49449651 | ||||||
chr15:49449806
|
T | TATAA | 277 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(274): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.286+25225_286+2522 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49449806 | |||||
chr15:49450046
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.286+25463T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450046 | ||||||
chr15:49450297
|
A | C | 173 | a0001c0001t0001g0054a0001c0001t0001g0192a0001c0001t0002g0001others(170): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.286+25714A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450297 | ||||||
chr15:49450483
|
A | G | 1 | a0001c0001t0009g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.286+25900A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450483 | ||||||
chr15:49450636
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+26053G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450636 | ||||||
chr15:49450714
|
A | G | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+26131A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450714 | ||||||
chr15:49450748
|
AT | A | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+26166delT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450748 | ||||||
chr15:49450758
|
G | A | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+26175G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450758 | ||||||
chr15:49450872
|
A | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(40): Show | 54 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.286+26289A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450872 | ||||||
chr15:49450881
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286+26298C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49450881 | ||||||
chr15:49451153
|
A | C | 2 | a0001c0001t0002g0087a0001c0001t0004g0019 | 3 | HG01099.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.286+26570A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451153 | ||||||
chr15:49451198
|
C | T | 25 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(22): Show | 33 | HG01516.hp2 HG01517.hp2 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.286+26615C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451198 | ||||||
chr15:49451379
|
G | T | 1 | a0001c0001t0006g0136 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.286+26796G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451379 | ||||||
chr15:49451385
|
T | C | 101 | a0001c0001t0001g0054a0001c0001t0002g0001a0001c0001t0002g0011others(98): Show | 126 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.286+26802T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451385 | ||||||
chr15:49451431
|
C | T | 84 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(81): Show | 102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.286+26848C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451431 | ||||||
chr15:49451814
|
C | T | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+27231C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451814 | ||||||
chr15:49451891
|
G | T | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+27308G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49451891 | ||||||
chr15:49452179
|
C | T | 84 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(81): Show | 102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.286+27596C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452179 | ||||||
chr15:49452186
|
T | C | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+27603T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452186 | ||||||
chr15:49452252
|
T | C | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+27669T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452252 | ||||||
chr15:49452273
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.286+27690G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452273 | ||||||
chr15:49452370
|
T | C | 176 | a0001c0001t0001g0054a0001c0001t0001g0119a0001c0001t0001g0192others(173): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.286+27787T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452370 | ||||||
chr15:49452522
|
T | A | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+27939T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452522 | ||||||
chr15:49452636
|
C | A | 3 | a0001c0001t0010g0281a0001c0001t0010g0282a0001c0001t0028g0280 | 3 | HG00408.hp1 HG02074.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.286+28053C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452636 | ||||||
chr15:49452662
|
T | C | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+28079T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452662 | ||||||
chr15:49452699
|
G | A | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+28116G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452699 | ||||||
chr15:49452744
|
C | T | 12 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.286+28161C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49452744 | ||||||
chr15:49453117
|
A | G | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+28534A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453117 | ||||||
chr15:49453223
|
G | A | 36 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(33): Show | 41 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.286+28640G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453223 | ||||||
chr15:49453235
|
C | A | 5 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG01109.hp2 HG02922.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+28652C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453235 | ||||||
chr15:49453378
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.286+28795A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453378 | ||||||
chr15:49453480
|
C | G | 23 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(20): Show | 30 | HG01943.hp2 HG02074.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.286+28897C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453480 | ||||||
chr15:49453514
|
T | G | 1 | a0001c0001t0003g0021 | 2 | NA19060.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.286+28931T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453514 | ||||||
chr15:49453556
|
C | T | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+28973C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453556 | ||||||
chr15:49453623
|
T | C | 1 | a0001c0001t0003g0144 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.286+29040T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453623 | ||||||
chr15:49453642
|
C | T | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.286+29059C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453642 | ||||||
chr15:49453684
|
C | T | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.286+29101C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453684 | ||||||
chr15:49453813
|
A | G | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+29230A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453813 | ||||||
chr15:49453908
|
G | A | 84 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(81): Show | 102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.287-29243G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453908 | ||||||
chr15:49453922
|
C | A | 1 | a0001c0001t0005g0270 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.287-29229C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453922 | ||||||
chr15:49453971
|
A | C | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.287-29180A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49453971 | ||||||
chr15:49454167
|
T | A | 60 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(57): Show | 67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-28984T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49454167 | ||||||
chr15:49454274
|
C | A | 1 | a0001c0001t0023g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.287-28877C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49454274 | ||||||
chr15:49454319
|
C | G | 1 | a0001c0001t0001g0165 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.287-28832C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49454319 | ||||||
chr15:49454377
|
T | A | 1 | a0001c0001t0001g0183 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287-28774T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49454377 | ||||||
chr15:49454898
|
T | C | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.287-28253T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49454898 | ||||||
chr15:49455029
|
G | A | 1 | a0001c0001t0010g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.287-28122G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455029 | ||||||
chr15:49455039
|
G | A | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.287-28112G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455039 | ||||||
chr15:49455090
|
CAT | C | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.287-28058_287-2805 others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49455090 | |||||
chr15:49455139
|
T | C | 1 | a0001c0001t0004g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.287-28012T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455139 | ||||||
chr15:49455148
|
G | A | 36 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(33): Show | 41 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.287-28003G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455148 | ||||||
chr15:49455288
|
G | A | 1 | a0001c0001t0003g0104 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.287-27863G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455288 | ||||||
chr15:49455426
|
C | G | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0126others(21): Show | 32 | HG01243.hp1 HG02273.hp2 HG02602.hp2 others(29): Show |
intron_variant | MODIFIER | c.287-27725C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455426 | ||||||
chr15:49455466
|
C | T | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.287-27685C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455466 | ||||||
chr15:49455537
|
T | C | 1 | a0001c0001t0003g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.287-27614T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455537 | ||||||
chr15:49455556
|
G | C | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0126others(21): Show | 32 | HG01243.hp1 HG02273.hp2 HG02602.hp2 others(29): Show |
intron_variant | MODIFIER | c.287-27595G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455556 | ||||||
chr15:49455606
|
C | T | 1 | a0001c0001t0025g0135 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.287-27545C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455606 | ||||||
chr15:49455632
|
TTAATC | T | 10 | a0001c0001t0005g0002a0001c0001t0005g0034a0001c0001t0005g0056others(7): Show | 15 | HG00558.hp1 HG01243.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.287-27514_287-2751 others(9): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49455632 | |||||
chr15:49455773
|
T | C | 24 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(21): Show | 26 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.287-27378T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455773 | ||||||
chr15:49455926
|
A | G | 17 | a0001c0001t0001g0054a0001c0001t0005g0002a0001c0001t0005g0015others(14): Show | 24 | HG00558.hp1 HG01070.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.287-27225A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49455926 | ||||||
chr15:49456065
|
A | T | 60 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(57): Show | 67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-27086A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456065 | ||||||
chr15:49456081
|
G | C | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-27070G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456081 | ||||||
chr15:49456123
|
A | C | 21 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0276others(18): Show | 23 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.287-27028A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456123 | ||||||
chr15:49456168
|
C | G | 83 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(80): Show | 101 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.287-26983C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456168 | ||||||
chr15:49456328
|
G | T | 12 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.287-26823G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456328 | ||||||
chr15:49456416
|
G | A | 60 | a0001c0001t0001g0192a0001c0001t0002g0085a0001c0001t0002g0087others(57): Show | 67 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.287-26735G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456416 | ||||||
chr15:49456593
|
C | G | 1 | a0001c0001t0003g0118 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.287-26558C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456593 | ||||||
chr15:49456658
|
A | C | 1 | a0001c0001t0002g0252 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.287-26493A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456658 | ||||||
chr15:49456761
|
T | C | 3 | a0001c0001t0008g0273a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.287-26390T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456761 | ||||||
chr15:49456899
|
C | T | 1 | a0001c0001t0028g0280 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.287-26252C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49456899 | ||||||
chr15:49457052
|
A | G | 1 | a0001c0001t0008g0292 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.287-26099A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457052 | ||||||
chr15:49457107
|
G | T | 31 | a0001c0001t0002g0085a0001c0001t0002g0087a0001c0001t0002g0251others(28): Show | 37 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.287-26044G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457107 | ||||||
chr15:49457243
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.287-25908C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457243 | ||||||
chr15:49457278
|
C | T | 18 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(15): Show | 19 | HG00408.hp1 HG01109.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.287-25873C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457278 | ||||||
chr15:49457351
|
T | C | 99 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(96): Show | 112 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.287-25800T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457351 | ||||||
chr15:49457529
|
A | G | 106 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(103): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.287-25622A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457529 | ||||||
chr15:49457538
|
C | T | 80 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(77): Show | 99 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.287-25613C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457538 | ||||||
chr15:49457581
|
T | A | 1 | a0001c0001t0016g0057 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.287-25570T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457581 | ||||||
chr15:49457621
|
T | C | 1 | a0001c0001t0008g0276 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.287-25530T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457621 | ||||||
chr15:49457877
|
CT | C | 32 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(29): Show | 40 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-25273delT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457877 | ||||||
chr15:49457882
|
C | G | 3 | a0001c0001t0002g0249a0001c0001t0002g0252a0001c0001t0002g0264 | 3 | HG00609.hp2 NA19012.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.287-25269C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457882 | ||||||
chr15:49457959
|
T | C | 1 | a0001c0001t0002g0227 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.287-25192T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49457959 | ||||||
chr15:49458210
|
A | G | 206 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(203): Show | 250 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.287-24941A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49458210 | ||||||
chr15:49458231
|
T | C | 95 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(92): Show | 113 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.287-24920T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49458231 | ||||||
chr15:49458283
|
A | AC | 20 | a0001c0001t0002g0226a0001c0001t0005g0002a0001c0001t0005g0015others(17): Show | 27 | HG00558.hp1 HG00733.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.287-24861dupC | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49458283 | |||||
chr15:49458389
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.287-24762C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49458389 | ||||||
chr15:49458987
|
C | T | 1 | a0001c0001t0004g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.287-24164C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49458987 | ||||||
chr15:49458988
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-24163G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49458988 | ||||||
chr15:49459028
|
C | G | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-24123C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459028 | ||||||
chr15:49459221
|
A | G | 4 | a0001c0001t0007g0133a0001c0001t0007g0178a0001c0001t0007g0179others(1): Show | 4 | HG02451.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-23930A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459221 | ||||||
chr15:49459361
|
A | G | 1 | a0001c0001t0007g0133 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.287-23790A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459361 | ||||||
chr15:49459429
|
T | C | 105 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(102): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-23722T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459429 | ||||||
chr15:49459476
|
GAA | G | 12 | a0001c0001t0012g0018a0001c0001t0012g0068a0001c0001t0012g0069others(9): Show | 13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-23672_287-2367 others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49459476 | |||||
chr15:49459511
|
A | G | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-23640A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459511 | ||||||
chr15:49459542
|
CT | C | 11 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(8): Show | 13 | HG00558.hp2 HG00642.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.287-23608delT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459542 | ||||||
chr15:49459656
|
A | G | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-23495A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459656 | ||||||
chr15:49459695
|
C | T | 105 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(102): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-23456C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459695 | ||||||
chr15:49459933
|
C | A | 1 | a0001c0001t0006g0124 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.287-23218C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49459933 | ||||||
chr15:49460066
|
C | T | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-23085C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49460066 | ||||||
chr15:49460497
|
T | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(203): Show | 250 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.287-22654T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49460497 | ||||||
chr15:49460548
|
T | C | 1 | a0001c0001t0013g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.287-22603T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49460548 | ||||||
chr15:49460759
|
T | C | 1 | a0001c0001t0014g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.287-22392T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49460759 | ||||||
chr15:49461079
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.287-22072C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49461079 | ||||||
chr15:49461335
|
T | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-21816T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49461335 | ||||||
chr15:49461450
|
C | T | 4 | a0001c0001t0012g0018a0001c0001t0012g0068a0001c0001t0012g0069others(1): Show | 5 | HG01255.hp1 HG02055.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-21701C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49461450 | ||||||
chr15:49461564
|
C | T | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-21587C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49461564 | ||||||
chr15:49461656
|
A | G | 1 | a0001c0001t0004g0083 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.287-21495A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49461656 | ||||||
chr15:49461951
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.287-21200C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49461951 | ||||||
chr15:49462254
|
G | A | 26 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0019others(23): Show | 32 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.287-20897G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462254 | ||||||
chr15:49462365
|
A | G | 107 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(104): Show | 125 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.287-20786A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462365 | ||||||
chr15:49462436
|
G | C | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-20715G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462436 | ||||||
chr15:49462527
|
T | C | 1 | a0001c0001t0010g0285 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.287-20624T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462527 | ||||||
chr15:49462547
|
C | G | 104 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(101): Show | 122 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.287-20604C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462547 | ||||||
chr15:49462599
|
T | C | 1 | a0001c0001t0002g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.287-20552T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462599 | ||||||
chr15:49462692
|
C | A | 1 | a0001c0001t0003g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.287-20459C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462692 | ||||||
chr15:49462822
|
G | A | 32 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(29): Show | 40 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-20329G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462822 | ||||||
chr15:49462870
|
TAA | T | 12 | a0001c0001t0012g0018a0001c0001t0012g0068a0001c0001t0012g0069others(9): Show | 13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-20279_287-2027 others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49462870 | |||||
chr15:49462955
|
G | T | 1 | a0001c0001t0002g0241 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.287-20196G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49462955 | ||||||
chr15:49463099
|
A | G | 11 | a0001c0001t0001g0192a0001c0001t0010g0281a0001c0001t0010g0282others(8): Show | 11 | HG00408.hp1 HG01255.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-20052A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463099 | ||||||
chr15:49463208
|
C | T | 1 | a0001c0001t0003g0023 | 2 | HG02074.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.287-19943C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463208 | ||||||
chr15:49463245
|
T | A | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-19906T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463245 | ||||||
chr15:49463252
|
C | A | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-19899C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463252 | ||||||
chr15:49463371
|
T | C | 1 | a0001c0001t0002g0208 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.287-19780T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463371 | ||||||
chr15:49463432
|
T | C | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-19719T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463432 | ||||||
chr15:49463476
|
G | A | 6 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0193others(3): Show | 6 | HG00741.hp1 HG01175.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-19675G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463476 | ||||||
chr15:49463550
|
C | CA | 36 | a0001c0001t0004g0006a0001c0001t0004g0076a0001c0001t0005g0002others(33): Show | 45 | HG00558.hp1 HG00609.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.287-19585dupA | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49463550 | |||||
chr15:49463550
|
C | CAAA | 62 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(59): Show | 76 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.287-19587_287-1958 others(7): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49463550 | |||||
chr15:49463550
|
C | CAAAA | 21 | a0001c0001t0002g0217a0001c0001t0002g0231a0001c0001t0002g0249others(18): Show | 25 | HG01169.hp1 HG01255.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.287-19588_287-1958 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49463550 | |||||
chr15:49463550
|
C | CAAAAA | 7 | a0001c0001t0007g0229a0001c0001t0012g0068a0001c0001t0013g0065others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-19589_287-1958 others(9): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49463550 | |||||
chr15:49463567
|
T | A | 105 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(102): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-19584T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463567 | ||||||
chr15:49463645
|
G | A | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-19506G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463645 | ||||||
chr15:49463884
|
A | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-19267A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463884 | ||||||
chr15:49463932
|
T | A | 62 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(59): Show | 79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.287-19219T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49463932 | ||||||
chr15:49463932
|
T | TTTTG | 93 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(90): Show | 110 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.287-19210_287-1920 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49463932 | |||||
chr15:49464064
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287-19087T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464064 | ||||||
chr15:49464178
|
T | C | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-18973T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464178 | ||||||
chr15:49464283
|
G | T | 62 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(59): Show | 79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.287-18868G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464283 | ||||||
chr15:49464572
|
T | C | 79 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(76): Show | 96 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.287-18579T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464572 | ||||||
chr15:49464789
|
C | T | 105 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(102): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-18362C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464789 | ||||||
chr15:49464812
|
C | T | 4 | a0001c0001t0002g0238a0001c0001t0002g0239a0001c0001t0002g0251others(1): Show | 4 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-18339C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464812 | ||||||
chr15:49464843
|
A | G | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-18308A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464843 | ||||||
chr15:49464900
|
T | C | 1 | a0001c0001t0007g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.287-18251T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464900 | ||||||
chr15:49464911
|
C | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-18240C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49464911 | ||||||
chr15:49465026
|
A | G | 4 | a0001c0001t0013g0065a0001c0001t0013g0066a0001c0001t0013g0067others(1): Show | 4 | HG02886.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-18125A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465026 | ||||||
chr15:49465188
|
A | G | 208 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(205): Show | 253 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.287-17963A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465188 | ||||||
chr15:49465269
|
A | G | 51 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(48): Show | 66 | HG00558.hp1 HG00733.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.287-17882A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465269 | ||||||
chr15:49465304
|
C | CT | 102 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(99): Show | 128 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.287-17833dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49465304 | |||||
chr15:49465561
|
T | C | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-17590T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465561 | ||||||
chr15:49465591
|
AAAAG | A | 102 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(99): Show | 120 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.287-17558_287-1755 others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49465591 | |||||
chr15:49465592
|
A | AGAGACCT others(4994): Show |
1 | a0001c0001t0002g0208 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.287-17559_287-1755 others(5005): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465592 | ||||||
chr15:49465595
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.287-17556G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465595 | ||||||
chr15:49465785
|
T | A | 80 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(77): Show | 97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.287-17366T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465785 | ||||||
chr15:49465801
|
C | T | 3 | a0001c0001t0002g0225a0001c0001t0002g0254a0001c0001t0027g0224 | 3 | HG02683.hp1 HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.287-17350C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465801 | ||||||
chr15:49465829
|
T | C | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-17322T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465829 | ||||||
chr15:49465974
|
A | G | 62 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(59): Show | 79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.287-17177A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49465974 | ||||||
chr15:49466231
|
G | A | 2 | a0001c0001t0004g0077a0001c0001t0004g0086 | 2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.287-16920G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49466231 | ||||||
chr15:49466302
|
T | C | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-16849T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49466302 | ||||||
chr15:49466496
|
T | C | 1 | a0001c0001t0004g0078 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.287-16655T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49466496 | ||||||
chr15:49466532
|
T | C | 38 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(35): Show | 47 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.287-16619T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49466532 | ||||||
chr15:49466539
|
T | C | 1 | a0001c0001t0020g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.287-16612T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49466539 | ||||||
chr15:49466794
|
T | C | 4 | a0001c0001t0003g0004a0001c0001t0003g0108a0001c0001t0003g0109others(1): Show | 7 | NA18961.hp1 NA18973.hp1 NA18987.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-16357T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49466794 | ||||||
chr15:49467083
|
G | T | 1 | a0001c0001t0004g0228 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.287-16068G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49467083 | ||||||
chr15:49467187
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.287-15964G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49467187 | ||||||
chr15:49467331
|
G | A | 1 | a0001c0001t0019g0022 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.287-15820G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49467331 | ||||||
chr15:49467460
|
C | CT | 3 | a0001c0001t0007g0178a0001c0001t0007g0179a0001c0001t0007g0184 | 3 | HG02451.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-15690dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49467460 | |||||
chr15:49467688
|
T | C | 3 | a0001c0001t0007g0261a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG02698.hp2 HG02738.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.287-15463T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49467688 | ||||||
chr15:49467732
|
A | G | 3 | a0001c0001t0009g0049a0001c0001t0009g0050a0001c0001t0009g0051 | 3 | HG01884.hp1 HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.287-15419A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49467732 | ||||||
chr15:49468144
|
A | G | 1 | a0001c0001t0001g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.287-15007A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468144 | ||||||
chr15:49468149
|
T | C | 62 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(59): Show | 79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.287-15002T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468149 | ||||||
chr15:49468228
|
G | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-14923G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468228 | ||||||
chr15:49468349
|
A | G | 206 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(203): Show | 250 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.287-14802A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468349 | ||||||
chr15:49468692
|
A | C | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-14459A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468692 | ||||||
chr15:49468807
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.287-14344C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468807 | ||||||
chr15:49468836
|
G | A | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-14315G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468836 | ||||||
chr15:49468867
|
A | T | 15 | a0001c0001t0006g0009a0001c0001t0006g0026a0001c0001t0006g0027others(12): Show | 21 | HG02273.hp2 HG02602.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.287-14284A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49468867 | ||||||
chr15:49469191
|
A | G | 1 | a0001c0001t0019g0022 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.287-13960A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49469191 | ||||||
chr15:49469564
|
T | C | 2 | a0001c0001t0002g0208a0001c0001t0003g0105 | 2 | NA18966.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.287-13587T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49469564 | ||||||
chr15:49469648
|
C | A | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-13503C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49469648 | ||||||
chr15:49469791
|
A | T | 105 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(102): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-13360A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49469791 | ||||||
chr15:49469965
|
T | C | 4 | a0001c0001t0011g0014a0001c0001t0011g0201a0001c0001t0011g0216others(1): Show | 6 | NA18957.hp1 NA18961.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-13186T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49469965 | ||||||
chr15:49470141
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.287-13010A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470141 | ||||||
chr15:49470245
|
T | TAACACTG others(2): Show |
261 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(258): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.287-12898_287-1289 others(13): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49470245 | |||||
chr15:49470417
|
T | C | 1 | a0001c0001t0006g0125 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.287-12734T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470417 | ||||||
chr15:49470497
|
A | G | 1 | a0001c0001t0004g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.287-12654A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470497 | ||||||
chr15:49470570
|
C | T | 4 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-12581C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470570 | ||||||
chr15:49470736
|
G | A | 13 | a0001c0001t0004g0193a0001c0001t0012g0018a0001c0001t0012g0068others(10): Show | 14 | HG01255.hp1 HG01358.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.287-12415G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470736 | ||||||
chr15:49470916
|
G | A | 6 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188others(3): Show | 6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-12235G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470916 | ||||||
chr15:49470925
|
C | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-12226C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470925 | ||||||
chr15:49470958
|
T | G | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-12193T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49470958 | ||||||
chr15:49471114
|
T | G | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.287-12037T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471114 | ||||||
chr15:49471269
|
T | TG | 238 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(235): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.287-11882_287-1188 others(5): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471269 | ||||||
chr15:49471283
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-11868G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471283 | ||||||
chr15:49471309
|
A | G | 1 | a0001c0001t0005g0061 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.287-11842A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471309 | ||||||
chr15:49471386
|
A | G | 210 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(207): Show | 254 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.287-11765A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471386 | ||||||
chr15:49471484
|
A | AAAT | 68 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(65): Show | 86 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.287-11620_287-1161 others(7): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | |||||
chr15:49471484
|
A | AAATAAT | 16 | a0001c0001t0002g0035a0001c0001t0002g0087a0001c0001t0002g0218others(13): Show | 16 | HG01099.hp1 HG01884.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.287-11623_287-1161 others(10): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | |||||
chr15:49471484
|
A | AAATAATA others(2): Show |
13 | a0001c0001t0001g0185a0001c0001t0002g0205a0001c0001t0002g0208others(10): Show | 13 | HG01081.hp2 HG01891.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-11626_287-1161 others(13): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | |||||
chr15:49471484
|
AAAT | A | 35 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(32): Show | 46 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.287-11620_287-1161 others(7): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | |||||
chr15:49471484
|
AAATAAT | A | 13 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0269others(10): Show | 16 | HG00733.hp2 HG02273.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.287-11623_287-1161 others(10): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | |||||
chr15:49471484
|
AAATAATA others(2): Show |
A | 47 | a0001c0001t0001g0025a0001c0001t0001g0126a0001c0001t0001g0127others(44): Show | 59 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.287-11626_287-1161 others(13): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | |||||
chr15:49471484
|
AAATAATA others(5): Show |
A | 20 | a0001c0001t0001g0142a0001c0001t0004g0007a0001c0001t0004g0019others(17): Show | 25 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-11629_287-1161 others(16): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | |||||
chr15:49471484
|
AAATAATA others(8): Show |
A | 3 | a0001c0001t0001g0139a0001c0001t0020g0274a0001c0001t0020g0275 | 3 | HG01358.hp1 HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-11632_287-1161 others(19): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49471484 | |||||
chr15:49471520
|
T | C | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-11631T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471520 | ||||||
chr15:49471537
|
C | A | 1 | a0001c0001t0002g0262 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.287-11614C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471537 | ||||||
chr15:49471546
|
T | C | 1 | a0001c0001t0003g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.287-11605T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471546 | ||||||
chr15:49471660
|
C | A | 4 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-11491C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471660 | ||||||
chr15:49471722
|
C | G | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-11429C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471722 | ||||||
chr15:49471768
|
C | T | 109 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-11383C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471768 | ||||||
chr15:49471885
|
A | T | 1 | a0001c0001t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.287-11266A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471885 | ||||||
chr15:49471904
|
G | A | 6 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188others(3): Show | 6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-11247G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471904 | ||||||
chr15:49471935
|
A | C | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-11216A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471935 | ||||||
chr15:49471965
|
A | T | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-11186A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49471965 | ||||||
chr15:49472020
|
GA | G | 250 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0031others(247): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.287-11117delA | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49472020 | |||||
chr15:49472020
|
GAA | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-11118_287-1111 others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49472020 | |||||
chr15:49472110
|
T | C | 1 | a0001c0001t0005g0056 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.287-11041T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49472110 | ||||||
chr15:49472225
|
T | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.287-10926T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49472225 | ||||||
chr15:49472442
|
A | G | 15 | a0001c0001t0006g0009a0001c0001t0006g0026a0001c0001t0006g0027others(12): Show | 21 | HG02273.hp2 HG02602.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.287-10709A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49472442 | ||||||
chr15:49472754
|
A | T | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-10397A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49472754 | ||||||
chr15:49472804
|
A | T | 62 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(59): Show | 79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.287-10347A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49472804 | ||||||
chr15:49472845
|
C | G | 2 | a0001c0001t0001g0119a0001c0001t0019g0022 | 3 | HG01516.hp2 HG01517.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.287-10306C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49472845 | ||||||
chr15:49472909
|
GTACCA | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-10238_287-1023 others(9): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49472909 | |||||
chr15:49473072
|
A | G | 4 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-10079A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473072 | ||||||
chr15:49473131
|
A | C | 1 | a0001c0001t0002g0222 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.287-10020A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473131 | ||||||
chr15:49473171
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.287-9980C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473171 | ||||||
chr15:49473182
|
G | A | 3 | a0001c0001t0007g0178a0001c0001t0007g0179a0001c0001t0007g0184 | 3 | HG02451.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.287-9969G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473182 | ||||||
chr15:49473229
|
C | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-9922C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473229 | ||||||
chr15:49473255
|
CATG | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-9889_287-9887d others(5): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49473255 | |||||
chr15:49473370
|
T | A | 4 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-9781T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473370 | ||||||
chr15:49473427
|
T | C | 1 | a0001c0001t0004g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.287-9724T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473427 | ||||||
chr15:49473543
|
T | C | 2 | a0001c0001t0010g0281a0001c0001t0010g0282 | 2 | HG00408.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.287-9608T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473543 | ||||||
chr15:49473565
|
C | T | 80 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(77): Show | 97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.287-9586C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473565 | ||||||
chr15:49473581
|
G | A | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-9570G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473581 | ||||||
chr15:49473617
|
C | T | 2 | a0001c0001t0014g0064a0001c0001t0014g0090 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.287-9534C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473617 | ||||||
chr15:49473620
|
A | G | 6 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188others(3): Show | 6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-9531A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473620 | ||||||
chr15:49473706
|
G | T | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-9445G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49473706 | ||||||
chr15:49474054
|
C | A | 26 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0019others(23): Show | 32 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.287-9097C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474054 | ||||||
chr15:49474152
|
C | T | 12 | a0001c0001t0012g0018a0001c0001t0012g0068a0001c0001t0012g0069others(9): Show | 13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-8999C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474152 | ||||||
chr15:49474286
|
C | T | 7 | a0001c0001t0001g0025a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 8 | HG01243.hp1 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-8865C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474286 | ||||||
chr15:49474588
|
T | A | 109 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-8563T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474588 | ||||||
chr15:49474660
|
G | T | 32 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(29): Show | 40 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-8491G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474660 | ||||||
chr15:49474771
|
G | A | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-8380G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474771 | ||||||
chr15:49474823
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0010g0282 | 2 | HG00408.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.287-8328G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474823 | ||||||
chr15:49474826
|
C | T | 2 | a0001c0001t0003g0037a0001c0001t0028g0280 | 3 | HG02074.hp2 HG02080.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.287-8325C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474826 | ||||||
chr15:49474869
|
C | T | 12 | a0001c0001t0012g0018a0001c0001t0012g0068a0001c0001t0012g0069others(9): Show | 13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-8282C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474869 | ||||||
chr15:49474886
|
C | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(62): Show | 81 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.287-8265C>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474886 | ||||||
chr15:49474937
|
C | T | 12 | a0001c0001t0012g0018a0001c0001t0012g0068a0001c0001t0012g0069others(9): Show | 13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-8214C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474937 | ||||||
chr15:49474964
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.287-8187T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49474964 | ||||||
chr15:49474996
|
A | AAAT | 21 | a0001c0001t0005g0002a0001c0001t0005g0015a0001c0001t0005g0016others(18): Show | 28 | HG00558.hp1 HG00558.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.287-8153_287-8152i others(5): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49474996 | |||||
chr15:49474998
|
AAGAT | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-8149_287-8146d others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49474998 | |||||
chr15:49475004
|
G | T | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-8147G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475004 | ||||||
chr15:49475120
|
T | C | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-8031T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475120 | ||||||
chr15:49475273
|
T | C | 210 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(207): Show | 254 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.287-7878T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475273 | ||||||
chr15:49475423
|
G | A | 12 | a0001c0001t0012g0018a0001c0001t0012g0068a0001c0001t0012g0069others(9): Show | 13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-7728G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475423 | ||||||
chr15:49475576
|
A | C | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-7575A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475576 | ||||||
chr15:49475614
|
A | AT | 105 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(102): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-7531dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49475614 | |||||
chr15:49475689
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.287-7462C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475689 | ||||||
chr15:49475728
|
T | C | 109 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-7423T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475728 | ||||||
chr15:49475927
|
C | T | 4 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-7224C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49475927 | ||||||
chr15:49476023
|
T | A | 1 | a0001c0001t0002g0236 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.287-7128T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476023 | ||||||
chr15:49476077
|
T | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-7074T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476077 | ||||||
chr15:49476164
|
G | C | 109 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-6987G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476164 | ||||||
chr15:49476171
|
A | C | 109 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-6980A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476171 | ||||||
chr15:49476212
|
G | GTTTT | 5 | a0001c0001t0001g0029a0001c0001t0001g0140a0001c0001t0001g0146others(2): Show | 6 | HG01074.hp2 HG03017.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-6938_287-6935d others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476212 | |||||
chr15:49476212
|
G | GTTTTT | 15 | a0001c0001t0001g0003a0001c0001t0001g0099a0001c0001t0001g0138others(12): Show | 18 | HG01099.hp2 HG01169.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.287-6935_287-6934i others(7): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476212 | |||||
chr15:49476212
|
G | GTTTTTT | 12 | a0001c0001t0001g0010a0001c0001t0001g0134a0001c0001t0001g0143others(9): Show | 14 | HG00323.hp2 HG01175.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.287-6935_287-6934i others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476212 | |||||
chr15:49476217
|
G | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(35): Show | 47 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.287-6934G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476217 | ||||||
chr15:49476219
|
TTTTTTGT others(6): Show |
T | 1 | a0001c0001t0001g0142 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.287-6926_287-6914d others(15): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476219 | |||||
chr15:49476225
|
G | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(35): Show | 47 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.287-6926G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476225 | ||||||
chr15:49476230
|
TG | T | 125 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(122): Show | 149 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.287-6919delG | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476230 | |||||
chr15:49476231
|
G | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(34): Show | 46 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.287-6920G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476231 | ||||||
chr15:49476231
|
GGT | G | 4 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0020g0274others(1): Show | 4 | HG02698.hp2 HG02738.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-6919_287-6918d others(4): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476231 | ||||||
chr15:49476232
|
G | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(76): Show | 99 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.287-6919G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476232 | ||||||
chr15:49476237
|
T | G | 1 | a0001c0001t0008g0277 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.287-6914T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476237 | ||||||
chr15:49476346
|
G | T | 1 | a0001c0001t0002g0245 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.287-6805G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476346 | ||||||
chr15:49476462
|
T | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-6689T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476462 | ||||||
chr15:49476522
|
A | C | 2 | a0001c0001t0005g0015a0001c0001t0005g0092 | 3 | NA18949.hp2 NA19082.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.287-6629A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476522 | ||||||
chr15:49476606
|
T | TAAC | 109 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-6543_287-6542i others(5): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476606 | |||||
chr15:49476624
|
T | C | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-6527T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476624 | ||||||
chr15:49476635
|
CATAA | C | 9 | a0001c0001t0008g0040a0001c0001t0008g0041a0001c0001t0008g0273others(6): Show | 11 | HG00642.hp1 HG02040.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-6507_287-6504d others(6): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49476635 | |||||
chr15:49476825
|
T | C | 109 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.287-6326T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476825 | ||||||
chr15:49476921
|
G | A | 1 | a0001c0001t0007g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.287-6230G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476921 | ||||||
chr15:49476937
|
G | A | 32 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(29): Show | 40 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-6214G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49476937 | ||||||
chr15:49477008
|
G | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(41): Show | 53 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.287-6143G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477008 | ||||||
chr15:49477020
|
A | G | 1 | a0001c0001t0028g0280 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.287-6131A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477020 | ||||||
chr15:49477037
|
G | C | 11 | a0001c0001t0009g0042a0001c0001t0009g0043a0001c0001t0009g0044others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.287-6114G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477037 | ||||||
chr15:49477060
|
G | GA | 8 | a0001c0001t0001g0143a0001c0001t0003g0107a0001c0001t0008g0041others(5): Show | 9 | HG02135.hp1 HG02622.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-6076dupA | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49477060 | |||||
chr15:49477060
|
G | GAAA | 97 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(94): Show | 115 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.287-6078_287-6076d others(5): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49477060 | |||||
chr15:49477169
|
C | G | 1 | a0001c0001t0002g0212 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.287-5982C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477169 | ||||||
chr15:49477172
|
C | T | 210 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(207): Show | 254 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.287-5979C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477172 | ||||||
chr15:49477265
|
G | C | 1 | a0001c0001t0008g0279 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.287-5886G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477265 | ||||||
chr15:49477371
|
T | C | 62 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(59): Show | 79 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.287-5780T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477371 | ||||||
chr15:49477412
|
A | G | 1 | a0001c0001t0010g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.287-5739A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477412 | ||||||
chr15:49477560
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0019g0022 | 3 | HG01516.hp2 HG01517.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.287-5591T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477560 | ||||||
chr15:49477619
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0019g0022 | 3 | HG01516.hp2 HG01517.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.287-5532G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477619 | ||||||
chr15:49477805
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.287-5346G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477805 | ||||||
chr15:49477911
|
A | G | 2 | a0001c0001t0002g0256a0001c0001t0002g0257 | 2 | HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.287-5240A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477911 | ||||||
chr15:49477972
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.287-5179T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49477972 | ||||||
chr15:49478070
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.287-5081A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478070 | ||||||
chr15:49478155
|
G | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-4996G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478155 | ||||||
chr15:49478419
|
G | A | 38 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(35): Show | 47 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.287-4732G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478419 | ||||||
chr15:49478457
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.287-4694C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478457 | ||||||
chr15:49478592
|
A | C | 1 | a0001c0001t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.287-4559A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478592 | ||||||
chr15:49478609
|
C | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-4542C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478609 | ||||||
chr15:49478755
|
T | G | 6 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188others(3): Show | 6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-4396T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478755 | ||||||
chr15:49478860
|
T | C | 6 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188others(3): Show | 6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-4291T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478860 | ||||||
chr15:49478965
|
T | A | 1 | a0001c0001t0002g0087 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.287-4186T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49478965 | ||||||
chr15:49479243
|
T | TTC | 105 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(102): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-3898_287-3897d others(4): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479243 | |||||
chr15:49479287
|
T | C | 30 | a0001c0001t0005g0002a0001c0001t0005g0015a0001c0001t0005g0016others(27): Show | 39 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.287-3864T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479287 | ||||||
chr15:49479360
|
G | A | 105 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(102): Show | 123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.287-3791G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479360 | ||||||
chr15:49479363
|
A | G | 290 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(287): Show | 350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.287-3788A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479363 | ||||||
chr15:49479423
|
C | G | 1 | a0001c0001t0019g0022 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.287-3728C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479423 | ||||||
chr15:49479451
|
G | A | 26 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0019others(23): Show | 32 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.287-3700G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479451 | ||||||
chr15:49479532
|
T | C | 1 | a0001c0001t0005g0056 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.287-3619T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479532 | ||||||
chr15:49479598
|
TG | T | 28 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(25): Show | 36 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(33): Show |
intron_variant | MODIFIER | c.287-3552delG | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479598 | ||||||
chr15:49479599
|
G | GT | 26 | a0001c0001t0001g0032a0001c0001t0001g0097a0001c0001t0001g0098others(23): Show | 34 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.287-3523dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | |||||
chr15:49479599
|
G | GTT | 6 | a0001c0001t0006g0114a0001c0001t0006g0123a0001c0001t0006g0136others(3): Show | 6 | HG03139.hp2 HG03942.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.287-3524_287-3523d others(4): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | |||||
chr15:49479599
|
G | GTTTTTTT others(2): Show |
8 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0045others(5): Show | 8 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-3531_287-3523d others(11): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | |||||
chr15:49479599
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0009g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287-3532_287-3523d others(12): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | |||||
chr15:49479599
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0009g0050 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.287-3533_287-3523d others(13): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | |||||
chr15:49479599
|
G | T | 4 | a0001c0001t0003g0100a0001c0001t0003g0110a0001c0001t0003g0116others(1): Show | 4 | HG04115.hp1 NA18979.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-3552G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479599 | ||||||
chr15:49479599
|
GT | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(52): Show | 72 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.287-3523delT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | |||||
chr15:49479599
|
GTTTTT | G | 8 | a0001c0001t0002g0036a0001c0001t0002g0039a0001c0001t0002g0205others(5): Show | 10 | HG00609.hp2 HG01952.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-3527_287-3523d others(7): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | |||||
chr15:49479599
|
GTTTTTT | G | 71 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(68): Show | 86 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.287-3528_287-3523d others(8): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | |||||
chr15:49479599
|
GTTTTTTT others(1): Show |
G | 12 | a0001c0001t0012g0018a0001c0001t0012g0068a0001c0001t0012g0069others(9): Show | 13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-3530_287-3523d others(10): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | |||||
chr15:49479599
|
GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0001g0167 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.287-3536_287-3523d others(16): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49479599 | |||||
chr15:49479612
|
T | G | 1 | a0001c0001t0008g0279 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.287-3539T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479612 | ||||||
chr15:49479780
|
A | C | 38 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(35): Show | 47 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.287-3371A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479780 | ||||||
chr15:49479810
|
C | T | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-3341C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479810 | ||||||
chr15:49479833
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.287-3318T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479833 | ||||||
chr15:49479840
|
C | T | 81 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(78): Show | 98 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.287-3311C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479840 | ||||||
chr15:49479899
|
C | T | 1 | a0001c0001t0003g0269 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.287-3252C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479899 | ||||||
chr15:49479922
|
A | T | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-3229A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49479922 | ||||||
chr15:49480040
|
T | C | 6 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188others(3): Show | 6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-3111T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480040 | ||||||
chr15:49480064
|
T | C | 1 | a0001c0001t0004g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.287-3087T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480064 | ||||||
chr15:49480071
|
T | C | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-3080T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480071 | ||||||
chr15:49480189
|
A | G | 25 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0019others(22): Show | 31 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.287-2962A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480189 | ||||||
chr15:49480393
|
T | C | 6 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188others(3): Show | 6 | HG02622.hp2 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-2758T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480393 | ||||||
chr15:49480474
|
A | AT | 186 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(183): Show | 230 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.287-2655dupT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49480474 | |||||
chr15:49480474
|
A | ATT | 23 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0002g0039others(20): Show | 25 | HG00099.hp2 HG01361.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-2656_287-2655d others(4): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49480474 | |||||
chr15:49480474
|
AT | A | 24 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0019others(21): Show | 30 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.287-2655delT | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49480474 | |||||
chr15:49480619
|
T | C | 4 | a0001c0001t0013g0065a0001c0001t0013g0066a0001c0001t0013g0067others(1): Show | 4 | HG02886.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-2532T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480619 | ||||||
chr15:49480706
|
T | C | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG02572.hp2 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-2445T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480706 | ||||||
chr15:49480708
|
C | T | 32 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(29): Show | 40 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-2443C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480708 | ||||||
chr15:49480798
|
T | C | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-2353T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480798 | ||||||
chr15:49480804
|
A | G | 2 | a0001c0001t0002g0243a0001c0001t0002g0247 | 2 | HG01928.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.287-2347A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49480804 | ||||||
chr15:49481031
|
A | C | 1 | a0001c0001t0002g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.287-2120A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481031 | ||||||
chr15:49481220
|
C | T | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-1931C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481220 | ||||||
chr15:49481340
|
T | G | 1 | a0001c0001t0015g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.287-1811T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481340 | ||||||
chr15:49481394
|
C | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.287-1757C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481394 | ||||||
chr15:49481532
|
A | G | 1 | a0001c0001t0007g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.287-1619A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481532 | ||||||
chr15:49481613
|
G | T | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(276): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.287-1538G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481613 | ||||||
chr15:49481678
|
T | A | 32 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(29): Show | 40 | HG01074.hp1 HG01943.hp2 HG02074.hp1 others(37): Show |
intron_variant | MODIFIER | c.287-1473T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481678 | ||||||
chr15:49481723
|
A | G | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-1428A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481723 | ||||||
chr15:49481859
|
T | A | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-1292T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49481859 | ||||||
chr15:49482148
|
G | C | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.287-1003G>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482148 | ||||||
chr15:49482228
|
A | C | 26 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0019others(23): Show | 32 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.287-923A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482228 | ||||||
chr15:49482284
|
G | GAT | 15 | a0001c0001t0006g0009a0001c0001t0006g0026a0001c0001t0006g0027others(12): Show | 21 | HG02273.hp2 HG02602.hp2 HG03491.hp2 others(18): Show |
intron_variant | MODIFIER | c.287-859_287-858dup others(2): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 49482284 | |||||
chr15:49482513
|
C | G | 1 | a0001c0001t0024g0121 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287-638C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482513 | ||||||
chr15:49482557
|
C | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(100): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.287-594C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482557 | ||||||
chr15:49482766
|
A | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(68): Show | 88 | HG00280.hp2 HG00323.hp2 HG01074.hp1 others(85): Show |
intron_variant | MODIFIER | c.287-385A>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482766 | ||||||
chr15:49482914
|
T | G | 4 | a0001c0001t0015g0186a0001c0001t0015g0187a0001c0001t0015g0188others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-237T>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482914 | ||||||
chr15:49482938
|
A | AC | 9 | a0001c0001t0007g0038a0001c0001t0007g0198a0001c0001t0007g0203others(6): Show | 10 | HG01169.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-213_287-212ins others(1): Show |
FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482938 | ||||||
chr15:49482939
|
T | A | 9 | a0001c0001t0007g0038a0001c0001t0007g0198a0001c0001t0007g0203others(6): Show | 10 | HG01169.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.287-212T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482939 | ||||||
chr15:49482950
|
C | T | 12 | a0001c0001t0012g0018a0001c0001t0012g0068a0001c0001t0012g0069others(9): Show | 13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-201C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 2/3 | chr15 | 49482950 | ||||||
chr15:49483369
|
A | T | 3 | a0001c0001t0015g0187a0001c0001t0015g0188a0001c0001t0015g0214 | 3 | HG02622.hp2 HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.390+115A>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483369 | ||||||
chr15:49483397
|
G | A | 39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 48 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.390+143G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483397 | ||||||
chr15:49483560
|
G | T | 26 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0019others(23): Show | 32 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.390+306G>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483560 | ||||||
chr15:49483832
|
T | C | 11 | a0001c0001t0001g0192a0001c0001t0010g0281a0001c0001t0010g0282others(8): Show | 11 | HG00408.hp1 HG01255.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.391-478T>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483832 | ||||||
chr15:49483922
|
C | G | 4 | a0001c0001t0012g0018a0001c0001t0012g0068a0001c0001t0012g0069others(1): Show | 5 | HG01255.hp1 HG02055.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-388C>G | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483922 | ||||||
chr15:49483987
|
G | A | 1 | a0001c0001t0014g0120 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.391-323G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483987 | ||||||
chr15:49483993
|
A | C | 1 | a0001c0001t0011g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-317A>C | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483993 | ||||||
chr15:49483998
|
T | A | 2 | a0001c0001t0020g0274a0001c0001t0020g0275 | 2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.391-312T>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49483998 | ||||||
chr15:49484234
|
C | T | 80 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(77): Show | 97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.391-76C>T | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49484234 | ||||||
chr15:49484292
|
G | A | 1 | a0001c0001t0006g0132 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.391-18G>A | FGF7 | ENSG00000140285.12 | transcript | ENST00000267843.9 | protein_coding | 3/3 | chr15 | 49484292 |