geneid | 2191 |
---|---|
ensemblid | ENSG00000078098.15 |
hgncid | 3590 |
symbol | FAP |
name | fibroblast activation protein alpha |
refseq_nuc | NM_004460.5 |
refseq_prot | NP_004451.2 |
ensembl_nuc | ENST00000188790.9 |
ensembl_prot | ENSP00000188790.4 |
mane_status | MANE Select |
chr | chr2 |
start | 162170684 |
end | 162243445 |
strand | - |
ver | v1.2 |
region | chr2:162170684-162243445 |
region5000 | chr2:162165684-162248445 |
regionname0 | FAP_chr2_162170684_162243445 |
regionname5000 | FAP_chr2_162165684_162248445 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 760 | 228 | 68 | 50 | 82 | 8 | 18 | 66 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0002 | 0/0 | 760 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0003 | 0/0 | 760 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0004 | 0/0 | 760 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2283 | 182 | 63 | 34 | 59 | 7 | 17 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
c0002 | 0/0 | 2283 | 36 | 0 | 14 | 21 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
c0003 | 0/0 | 2283 | 5 | 5 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
c0004 | 0/0 | 2283 | 3 | 0 | 0 | 2 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
c0005 | 0/0 | 2283 | 3 | 3 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
c0006 | 0/0 | 2283 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
c0007 | 0/0 | 2283 | 2 | 0 | 2 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
c0008 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 414 | 229 | 69 | 50 | 82 | 8 | 18 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
t0002 | 0/0 | 414 | 3 | 3 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
t0003 | 0/0 | 414 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2283 | 182 | 63 | 34 | 59 | 7 | 17 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0001c0002 | 0/0 | 2283 | 36 | 0 | 14 | 21 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0001c0003 | 0/0 | 2283 | 5 | 5 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0001c0004 | 0/0 | 2283 | 3 | 0 | 0 | 2 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0001c0007 | 0/0 | 2283 | 2 | 0 | 2 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0002c0005 | 0/0 | 2283 | 3 | 3 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0003c0006 | 0/0 | 2283 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0004c0008 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2696 | 179 | 60 | 34 | 59 | 7 | 17 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0001c0001t0002 | 0/0 | 2696 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0001c0001t0003 | 0/0 | 2696 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0001c0002t0001 | 0/0 | 2696 | 36 | 0 | 14 | 21 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0001c0003t0001 | 0/0 | 2696 | 5 | 5 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0001c0004t0001 | 0/0 | 2696 | 3 | 0 | 0 | 2 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0001c0007t0001 | 0/0 | 2696 | 2 | 0 | 2 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0002c0005t0001 | 0/0 | 2696 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0002c0005t0002 | 0/0 | 2696 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0003c0006t0001 | 0/0 | 2696 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
a0004c0008t0001 | 0/0 | 2696 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | copy fasta | chr2 | 162165684 | 162248445 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0004t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0007t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0001c0007t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0002c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0002c0005t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0002c0005t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0003c0006t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0003c0006t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
a0004c0008t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | FIN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | CHS | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01257 | hp2 | a0001 | c0007 | t0001 | g0052 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01258 | hp1 | a0001 | c0007 | t0001 | g0053 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02280 | hp1 | a0002 | c0005 | t0001 | g0061 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0077 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02630 | hp2 | a0003 | c0006 | t0001 | g0196 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0074 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0079 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03139 | hp2 | a0004 | c0008 | t0001 | g0017 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03209 | hp1 | a0002 | c0005 | t0002 | g0216 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03486 | hp2 | a0002 | c0005 | t0002 | g0215 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18952 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | LWK | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19085 | hp1 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | YRI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ASW | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA20805 | hp1 | a0001 | c0004 | t0001 | g0093 | EUR | TSI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | GIH | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | GIH | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02559 | hp1 | a0003 | c0006 | t0001 | g0084 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0075 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | USA | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | USA | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | USA | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | USA | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | LWK | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0194 | REF | REF | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0090 | REF | REF | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:162218062
|
G | A | 1 | a0004 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.686C>T | p.Thr229Met | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/26 | 804/2696 | 686/2283 | 229/760 | chr2 | 162218062 | ||
chr2:162218114
|
G | A | 1 | a0002 | 3 | HG02280.hp1 HG03209.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.634C>T | p.Leu212Phe | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/26 | 752/2696 | 634/2283 | 212/760 | chr2 | 162218114 | ||
chr2:162225536
|
G | T | 1 | a0003 | 2 | HG02559.hp1 HG02630.hp2 |
missense_variant | MODERATE | c.232C>A | p.Leu78Ile | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/26 | 350/2696 | 232/2283 | 78/760 | chr2 | 162225536 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:162171060
|
G | A | 1 | a0001c0007 | 2 | HG01257.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.2202C>T | p.His734His | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 26/26 | 2320/2696 | 2202/2283 | 734/760 | chr2 | 162171060 | ||
chr2:162173786
|
C | T | 1 | a0001c0004 | 3 | NA18952.hp2 NA19085.hp1 NA20805.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1971G>A | p.Ala657Ala | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 23/26 | 2089/2696 | 1971/2283 | 657/760 | chr2 | 162173786 | ||
chr2:162198785
|
G | A | 1 | a0002c0005 | 3 | HG02280.hp1 HG03209.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.1374C>T | p.Tyr458Tyr | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/26 | 1492/2696 | 1374/2283 | 458/760 | chr2 | 162198785 | ||
chr2:162219085
|
T | G | 1 | a0001c0003 | 5 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
synonymous_variant | LOW | c.585A>C | p.Gly195Gly | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/26 | 703/2696 | 585/2283 | 195/760 | chr2 | 162219085 | ||
chr2:162224472
|
A | G | 1 | a0001c0002 | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
synonymous_variant | LOW | c.354T>C | p.Tyr118Tyr | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 5/26 | 472/2696 | 354/2283 | 118/760 | chr2 | 162224472 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:162243397
|
G | A | 2 | a0001c0001t0002a0002c0005t0002 | 3 | HG03209.hp1 HG03486.hp2 NA21309.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-70C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 1/26 | chr2 | 162243397 | ||||||
chr2:162243414
|
C | A | 1 | a0001c0001t0003 | 2 | HG02970.hp2 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-87G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 1/26 | 87 | chr2 | 162243414 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:162171308
|
G | A | 23 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0086others(20): Show | 25 | HG00609.hp1 HG00621.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.2182-228C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162171308 | ||||||
chr2:162171809
|
CT | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(57): Show | 68 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.2182-730delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162171809 | ||||||
chr2:162171813
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2182-733A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162171813 | ||||||
chr2:162171935
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0089others(1): Show | 4 | HG02970.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2182-855A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162171935 | ||||||
chr2:162171980
|
T | C | 39 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0086others(36): Show | 42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.2181+831A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162171980 | ||||||
chr2:162172174
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2181+637T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162172174 | ||||||
chr2:162172378
|
A | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(66): Show | 77 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.2181+433T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162172378 | ||||||
chr2:162173644
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2034+79A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 23/25 | chr2 | 162173644 | ||||||
chr2:162173826
|
T | C | 33 | a0001c0001t0001g0054a0001c0001t0001g0059a0001c0001t0001g0076others(30): Show | 33 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1970-39A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 22/25 | chr2 | 162173826 | ||||||
chr2:162174025
|
A | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0131 | 3 | HG02071.hp1 HG02083.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1970-238T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 22/25 | chr2 | 162174025 | ||||||
chr2:162174200
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0072a0001c0001t0001g0146others(5): Show | 8 | HG02155.hp2 HG02273.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1970-413G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 22/25 | chr2 | 162174200 | ||||||
chr2:162174494
|
G | A | 18 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0062others(15): Show | 22 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1969+373C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 22/25 | chr2 | 162174494 | ||||||
chr2:162174527
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1969+340C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 22/25 | chr2 | 162174527 | ||||||
chr2:162174834
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1969+33G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 22/25 | chr2 | 162174834 | ||||||
chr2:162175519
|
T | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 231 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1870-553A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162175519 | ||||||
chr2:162175548
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1870-582C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162175548 | ||||||
chr2:162175578
|
T | C | 2 | a0003c0006t0001g0084a0003c0006t0001g0196 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1870-612A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162175578 | ||||||
chr2:162175824
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(57): Show | 68 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.1870-858G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162175824 | ||||||
chr2:162176261
|
T | G | 1 | a0001c0001t0001g0150 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1870-1295A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162176261 | ||||||
chr2:162177039
|
TGAA | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0072a0001c0001t0001g0146others(5): Show | 8 | HG02155.hp2 HG02273.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1870-2076_1870-207 others(7): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162177039 | ||||||
chr2:162177067
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1870-2101A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162177067 | ||||||
chr2:162177611
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1870-2645A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162177611 | ||||||
chr2:162177643
|
C | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0062others(15): Show | 22 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1870-2677G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162177643 | ||||||
chr2:162177951
|
T | C | 39 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0086others(36): Show | 42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1870-2985A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162177951 | ||||||
chr2:162178060
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1870-3094G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162178060 | ||||||
chr2:162178479
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 6 | HG00558.hp2 HG00609.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1870-3513C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162178479 | ||||||
chr2:162178497
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1870-3531G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162178497 | ||||||
chr2:162178581
|
G | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0144a0001c0001t0001g0205 | 3 | HG02922.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1870-3615C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162178581 | ||||||
chr2:162178698
|
TC | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0210 | 2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1870-3733delG | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162178698 | ||||||
chr2:162179245
|
G | GT | 5 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0119others(2): Show | 5 | HG00741.hp2 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1869+4168dupA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179245 | ||||||
chr2:162179245
|
GT | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 173 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1869+4168delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179245 | ||||||
chr2:162179245
|
GTT | G | 25 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0086others(22): Show | 27 | HG00609.hp1 HG00621.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.1869+4167_1869+416 others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179245 | ||||||
chr2:162179277
|
A | G | 3 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156 | 3 | HG02155.hp2 NA18959.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1869+4137T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179277 | ||||||
chr2:162179431
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1869+3983G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179431 | ||||||
chr2:162179466
|
A | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0062others(7): Show | 14 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1869+3948T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179466 | ||||||
chr2:162179708
|
A | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0208a0001c0001t0003g0218 | 3 | HG02451.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1869+3706T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179708 | ||||||
chr2:162179759
|
G | GATCT | 4 | a0001c0001t0001g0184a0001c0003t0001g0077a0002c0005t0002g0215others(1): Show | 4 | HG01168.hp1 HG02622.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1869+3651_1869+365 others(8): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179759 | ||||||
chr2:162179759
|
G | GATCTATC others(1): Show |
4 | a0001c0001t0001g0110a0001c0001t0001g0213a0001c0001t0003g0217others(1): Show | 4 | HG02258.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1869+3647_1869+365 others(12): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179759 | ||||||
chr2:162179759
|
G | GATCTATC others(5): Show |
3 | a0001c0001t0001g0199a0001c0003t0001g0078a0001c0003t0001g0079 | 3 | HG02630.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1869+3643_1869+365 others(16): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179759 | ||||||
chr2:162179779
|
T | TATC | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1869+3632_1869+363 others(7): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179779 | ||||||
chr2:162179782
|
CTATCTAT others(5): Show |
C | 1 | a0001c0001t0002g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1869+3620_1869+363 others(16): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179782 | ||||||
chr2:162179786
|
CTATCTA | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0073 | 2 | HG02451.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1869+3622_1869+362 others(10): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179786 | ||||||
chr2:162179787
|
T | A | 1 | a0001c0001t0001g0069 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1869+3627A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179787 | ||||||
chr2:162179787
|
T | TATCA | 2 | a0001c0001t0001g0164a0001c0001t0001g0167 | 2 | HG00733.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.1869+3626_1869+362 others(8): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179787 | ||||||
chr2:162179788
|
ATC | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0174 | 2 | NA19007.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1869+3624_1869+362 others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179788 | ||||||
chr2:162179790
|
C | CAA | 23 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(20): Show | 27 | HG00140.hp1 HG00323.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1869+3623_1869+362 others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179790 | ||||||
chr2:162179790
|
CTA | C | 69 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0055others(66): Show | 71 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1869+3622_1869+362 others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179790 | ||||||
chr2:162179791
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1869+3623A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179791 | ||||||
chr2:162179792
|
A | ATC | 8 | a0001c0001t0001g0006a0001c0001t0001g0070a0001c0001t0001g0099others(5): Show | 9 | HG01258.hp2 HG01346.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1869+3621_1869+362 others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179792 | ||||||
chr2:162179792
|
A | ATCTATC | 11 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0118others(8): Show | 13 | HG00735.hp2 HG01891.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1869+3621_1869+362 others(10): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179792 | ||||||
chr2:162179792
|
A | ATCTATCT others(3): Show |
4 | a0001c0001t0001g0020a0001c0001t0001g0096a0001c0001t0001g0191others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+3621_1869+362 others(14): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179792 | ||||||
chr2:162179792
|
A | C | 23 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(20): Show | 27 | HG00140.hp1 HG00323.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1869+3622T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179792 | ||||||
chr2:162179794
|
A | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(77): Show | 87 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1869+3620T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179794 | ||||||
chr2:162179796
|
A | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0013others(8): Show | 14 | HG00639.hp1 HG00735.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1869+3618T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179796 | ||||||
chr2:162179798
|
A | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0063others(20): Show | 27 | HG00639.hp2 HG01106.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1869+3616T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179798 | ||||||
chr2:162179800
|
A | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 4 | HG00735.hp2 HG01258.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1869+3614T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179800 | ||||||
chr2:162179800
|
ATATATAT others(6): Show |
A | 1 | a0001c0002t0001g0021 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1869+3601_1869+361 others(17): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179800 | ||||||
chr2:162179802
|
A | C | 3 | a0001c0001t0001g0018a0001c0002t0001g0044a0001c0002t0001g0048 | 3 | HG02258.hp1 NA18975.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1869+3612T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179802 | ||||||
chr2:162179804
|
ATATATAT others(2): Show |
A | 25 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0098others(22): Show | 27 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1869+3601_1869+360 others(13): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179804 | ||||||
chr2:162179808
|
A | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0065a0002c0005t0001g0061 | 3 | HG02280.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1869+3606T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179808 | ||||||
chr2:162179808
|
ATATAT | A | 8 | a0001c0001t0001g0086a0001c0002t0001g0003a0001c0002t0001g0027others(5): Show | 9 | HG01175.hp1 HG02004.hp2 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.1869+3601_1869+360 others(9): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179808 | ||||||
chr2:162179809
|
TA | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1869+3604delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179809 | ||||||
chr2:162179809
|
TATA | T | 4 | a0001c0001t0001g0091a0001c0001t0001g0102a0001c0001t0001g0124others(1): Show | 4 | HG02602.hp1 HG03490.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1869+3602_1869+360 others(7): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179809 | ||||||
chr2:162179810
|
A | ATTTT | 6 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0063others(3): Show | 9 | HG01106.hp1 HG01261.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1869+3603_1869+360 others(8): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179810 | ||||||
chr2:162179810
|
A | ATTTTTTT others(40): Show |
1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1869+3603_1869+360 others(51): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179810 | ||||||
chr2:162179810
|
A | T | 11 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0065others(8): Show | 11 | HG02258.hp2 HG02280.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1869+3604T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179810 | ||||||
chr2:162179812
|
A | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(53): Show | 61 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1869+3602T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179812 | ||||||
chr2:162179813
|
T | TA | 7 | a0001c0001t0001g0096a0001c0001t0001g0120a0001c0001t0001g0165others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1869+3600_1869+360 others(5): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179813 | ||||||
chr2:162179813
|
T | TATA | 2 | a0001c0001t0001g0171a0001c0001t0001g0189 | 2 | HG00733.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1869+3600_1869+360 others(7): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179813 | ||||||
chr2:162179814
|
T | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0121a0001c0001t0001g0164others(3): Show | 7 | HG00733.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1869+3600A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179814 | ||||||
chr2:162179816
|
T | A | 4 | a0001c0001t0001g0011a0001c0001t0003g0218a0002c0005t0002g0215others(1): Show | 5 | HG02896.hp2 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1869+3598A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179816 | ||||||
chr2:162179839
|
C | T | 2 | a0001c0001t0001g0113a0001c0002t0001g0045 | 2 | HG00140.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1869+3575G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179839 | ||||||
chr2:162179869
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(61): Show | 72 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1869+3545A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179869 | ||||||
chr2:162180028
|
C | T | 10 | a0001c0001t0001g0185a0001c0002t0001g0002a0001c0002t0001g0024others(7): Show | 11 | HG01069.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1869+3386G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162180028 | ||||||
chr2:162180092
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1869+3322C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162180092 | ||||||
chr2:162180107
|
A | G | 39 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0086others(36): Show | 42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1869+3307T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162180107 | ||||||
chr2:162180309
|
A | T | 1 | a0001c0001t0001g0119 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1869+3105T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162180309 | ||||||
chr2:162180350
|
C | A | 1 | a0001c0001t0001g0069 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1869+3064G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162180350 | ||||||
chr2:162180830
|
T | A | 1 | a0001c0002t0001g0044 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1869+2584A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162180830 | ||||||
chr2:162181044
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1869+2370C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181044 | ||||||
chr2:162181170
|
A | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(61): Show | 72 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1869+2244T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181170 | ||||||
chr2:162181255
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1869+2159G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181255 | ||||||
chr2:162181392
|
C | G | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1869+2022G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181392 | ||||||
chr2:162181416
|
A | G | 18 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0062others(15): Show | 22 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1869+1998T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181416 | ||||||
chr2:162181517
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1869+1897A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181517 | ||||||
chr2:162181872
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0154 | 3 | NA18992.hp1 NA18994.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1869+1542C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181872 | ||||||
chr2:162181915
|
T | A | 20 | a0001c0001t0001g0073a0001c0001t0001g0087a0001c0001t0001g0088others(17): Show | 21 | HG02074.hp2 HG02083.hp2 HG03017.hp1 others(18): Show |
intron_variant | MODIFIER | c.1869+1499A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181915 | ||||||
chr2:162182113
|
G | C | 1 | a0001c0001t0002g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1869+1301C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162182113 | ||||||
chr2:162182309
|
C | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0038 | 2 | HG01175.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1869+1105G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162182309 | ||||||
chr2:162183091
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1869+323T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162183091 | ||||||
chr2:162183256
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1869+158G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162183256 | ||||||
chr2:162183576
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1815-108G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162183576 | ||||||
chr2:162183644
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1815-176C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162183644 | ||||||
chr2:162183730
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1815-262G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162183730 | ||||||
chr2:162183731
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0003g0217 | 3 | HG02970.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1815-263C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162183731 | ||||||
chr2:162183771
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1815-303A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162183771 | ||||||
chr2:162184248
|
G | A | 2 | a0002c0005t0002g0215a0002c0005t0002g0216 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1815-780C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162184248 | ||||||
chr2:162184515
|
A | T | 1 | a0001c0002t0001g0030 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1815-1047T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162184515 | ||||||
chr2:162184772
|
TA | T | 39 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0086others(36): Show | 42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1815-1305delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162184772 | ||||||
chr2:162184877
|
T | G | 39 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0086others(36): Show | 42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1815-1409A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162184877 | ||||||
chr2:162184894
|
A | G | 13 | a0001c0001t0001g0110a0001c0001t0001g0181a0001c0001t0001g0182others(10): Show | 13 | HG01168.hp1 HG01192.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1815-1426T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162184894 | ||||||
chr2:162185074
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0003g0218 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1815-1606G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162185074 | ||||||
chr2:162185171
|
A | G | 2 | a0001c0003t0001g0074a0001c0003t0001g0075 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1815-1703T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162185171 | ||||||
chr2:162185301
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1815-1833A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162185301 | ||||||
chr2:162185313
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0174a0001c0001t0001g0212 | 3 | NA19004.hp2 NA19007.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1815-1845G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162185313 | ||||||
chr2:162185510
|
G | A | 2 | a0001c0001t0001g0208a0001c0001t0003g0218 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1815-2042C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162185510 | ||||||
chr2:162185977
|
C | T | 1 | a0004c0008t0001g0017 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1814+2192G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162185977 | ||||||
chr2:162186131
|
T | C | 2 | a0001c0001t0001g0208a0001c0001t0003g0218 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1814+2038A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186131 | ||||||
chr2:162186410
|
T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0209 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1814+1759A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186410 | ||||||
chr2:162186426
|
A | G | 1 | a0001c0002t0001g0046 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1814+1743T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186426 | ||||||
chr2:162186585
|
C | T | 1 | a0001c0002t0001g0027 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1814+1584G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186585 | ||||||
chr2:162186651
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1814+1518C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186651 | ||||||
chr2:162186712
|
C | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1814+1457G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186712 | ||||||
chr2:162186775
|
C | T | 5 | a0001c0002t0001g0003a0001c0002t0001g0040a0001c0002t0001g0044others(2): Show | 6 | NA18975.hp2 NA19004.hp1 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.1814+1394G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186775 | ||||||
chr2:162186818
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1814+1351C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186818 | ||||||
chr2:162186831
|
T | TA | 2 | a0001c0001t0001g0011a0001c0001t0001g0169 | 3 | HG02896.hp2 HG02897.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1814+1337_1814+133 others(5): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186831 | ||||||
chr2:162186842
|
C | CACTCCTA others(5): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0169 | 3 | HG02896.hp2 HG02897.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1814+1326_1814+132 others(16): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186842 | ||||||
chr2:162187169
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1814+1000G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187169 | ||||||
chr2:162187218
|
C | A | 1 | a0001c0001t0001g0207 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1814+951G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187218 | ||||||
chr2:162187243
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1814+926C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187243 | ||||||
chr2:162187357
|
A | T | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1814+812T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187357 | ||||||
chr2:162187360
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1814+809G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187360 | ||||||
chr2:162187511
|
G | T | 39 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0086others(36): Show | 42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1814+658C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187511 | ||||||
chr2:162187561
|
G | A | 2 | a0001c0001t0001g0208a0001c0001t0003g0218 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1814+608C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187561 | ||||||
chr2:162187641
|
C | A | 2 | a0002c0005t0002g0215a0002c0005t0002g0216 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1814+528G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187641 | ||||||
chr2:162187709
|
A | T | 39 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0086others(36): Show | 42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1814+460T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187709 | ||||||
chr2:162187845
|
G | A | 39 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0086others(36): Show | 42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1814+324C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187845 | ||||||
chr2:162187880
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0089others(1): Show | 4 | HG02970.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1814+289C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187880 | ||||||
chr2:162188384
|
A | T | 1 | a0001c0001t0001g0013 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1620-21T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162188384 | ||||||
chr2:162188460
|
T | A | 1 | a0001c0001t0001g0174 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1620-97A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162188460 | ||||||
chr2:162188769
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1619+334A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162188769 | ||||||
chr2:162188922
|
A | C | 1 | a0001c0001t0001g0207 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1619+181T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162188922 | ||||||
chr2:162188948
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1619+155G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162188948 | ||||||
chr2:162189002
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1619+101G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162189002 | ||||||
chr2:162189052
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1619+51A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162189052 | ||||||
chr2:162189181
|
A | G | 2 | a0001c0001t0001g0208a0001c0001t0003g0218 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1550-9T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189181 | ||||||
chr2:162189323
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1550-151A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189323 | ||||||
chr2:162189424
|
C | T | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG00621.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1549+232G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189424 | ||||||
chr2:162189458
|
A | T | 1 | a0001c0001t0002g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1549+198T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189458 | ||||||
chr2:162189533
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+123A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189533 | ||||||
chr2:162189534
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+122C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189534 | ||||||
chr2:162189538
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+118A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189538 | ||||||
chr2:162189539
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+117G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189539 | ||||||
chr2:162189540
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+116G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189540 | ||||||
chr2:162189541
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+115A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189541 | ||||||
chr2:162189542
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+114C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189542 | ||||||
chr2:162189543
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+113A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189543 | ||||||
chr2:162189546
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+110A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189546 | ||||||
chr2:162189548
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+108A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189548 | ||||||
chr2:162189549
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+107A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189549 | ||||||
chr2:162189553
|
A | T | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+103T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189553 | ||||||
chr2:162189554
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+102C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189554 | ||||||
chr2:162189556
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+100A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189556 | ||||||
chr2:162189557
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+99G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189557 | ||||||
chr2:162189558
|
G | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0117 | 2 | HG02258.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1549+98C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189558 | ||||||
chr2:162189559
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+97G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189559 | ||||||
chr2:162189561
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+95C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189561 | ||||||
chr2:162189564
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+92A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189564 | ||||||
chr2:162189565
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+91A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189565 | ||||||
chr2:162189566
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+90A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189566 | ||||||
chr2:162189567
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+89C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189567 | ||||||
chr2:162189568
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+88G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189568 | ||||||
chr2:162189570
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+86G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189570 | ||||||
chr2:162189571
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+85A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189571 | ||||||
chr2:162189572
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+84C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189572 | ||||||
chr2:162189573
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+83A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189573 | ||||||
chr2:162189576
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+80G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189576 | ||||||
chr2:162189580
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+76G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189580 | ||||||
chr2:162189582
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+74G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189582 | ||||||
chr2:162189584
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+72G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189584 | ||||||
chr2:162189585
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+71A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189585 | ||||||
chr2:162189587
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+69A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189587 | ||||||
chr2:162189588
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+68C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189588 | ||||||
chr2:162189589
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+67G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189589 | ||||||
chr2:162189590
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+66A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189590 | ||||||
chr2:162189591
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+65A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189591 | ||||||
chr2:162189592
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+64A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189592 | ||||||
chr2:162189593
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+63A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189593 | ||||||
chr2:162189594
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+62A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189594 | ||||||
chr2:162189595
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+61A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189595 | ||||||
chr2:162189798
|
T | A | 1 | a0001c0001t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1451-44A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162189798 | ||||||
chr2:162189837
|
T | A | 2 | a0001c0001t0001g0208a0001c0001t0003g0218 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1451-83A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162189837 | ||||||
chr2:162190036
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0099 | 3 | HG01258.hp2 HG01346.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1451-282G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162190036 | ||||||
chr2:162190357
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1451-603C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162190357 | ||||||
chr2:162190395
|
T | TAC | 4 | a0001c0001t0001g0016a0001c0001t0001g0056a0001c0001t0001g0083others(1): Show | 4 | HG00741.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1451-643_1451-642d others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162190395 | ||||||
chr2:162190395
|
TAC | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0176a0001c0001t0003g0217 | 3 | HG01361.hp1 HG02602.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1451-643_1451-642d others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162190395 | ||||||
chr2:162190527
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1451-773T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162190527 | ||||||
chr2:162190740
|
T | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG00621.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1451-986A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162190740 | ||||||
chr2:162191073
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1451-1319C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191073 | ||||||
chr2:162191329
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1451-1575C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191329 | ||||||
chr2:162191331
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1451-1577T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191331 | ||||||
chr2:162191375
|
C | T | 20 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(17): Show | 25 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1451-1621G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191375 | ||||||
chr2:162191438
|
A | G | 23 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0086others(20): Show | 25 | HG00609.hp1 HG00621.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.1451-1684T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191438 | ||||||
chr2:162191542
|
A | AGCACCTA others(7): Show |
1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1451-1802_1451-178 others(18): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191542 | ||||||
chr2:162191624
|
G | T | 2 | a0001c0001t0001g0120a0001c0001t0001g0193 | 2 | HG02622.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1451-1870C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191624 | ||||||
chr2:162191787
|
G | T | 1 | a0001c0001t0001g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1451-2033C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191787 | ||||||
chr2:162191894
|
C | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(22): Show | 30 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1451-2140G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191894 | ||||||
chr2:162192461
|
C | A | 3 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0186 | 3 | HG01168.hp1 HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1450+2240G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162192461 | ||||||
chr2:162192496
|
C | T | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1450+2205G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162192496 | ||||||
chr2:162192508
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0089others(1): Show | 4 | HG02970.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450+2193C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162192508 | ||||||
chr2:162192603
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1450+2098A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162192603 | ||||||
chr2:162193129
|
T | C | 39 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0086others(36): Show | 42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1450+1572A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193129 | ||||||
chr2:162193166
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1450+1535C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193166 | ||||||
chr2:162193242
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0188 | 2 | HG00558.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1450+1459G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193242 | ||||||
chr2:162193289
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1450+1412T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193289 | ||||||
chr2:162193397
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1450+1304C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193397 | ||||||
chr2:162193400
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1450+1301C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193400 | ||||||
chr2:162193498
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1450+1203T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193498 | ||||||
chr2:162193693
|
AC | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0149 | 3 | HG01358.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1450+1007delG | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193693 | ||||||
chr2:162193964
|
T | C | 18 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0062others(15): Show | 22 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1450+737A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193964 | ||||||
chr2:162193988
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1450+713T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193988 | ||||||
chr2:162194153
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1450+548C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194153 | ||||||
chr2:162194272
|
C | CCA | 36 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0089others(33): Show | 37 | HG00558.hp1 HG00621.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.1450+427_1450+428d others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194272 | ||||||
chr2:162194272
|
C | CCACA | 18 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(15): Show | 23 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1450+425_1450+428d others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194272 | ||||||
chr2:162194272
|
C | CCACACA | 5 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0199others(2): Show | 6 | HG02258.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1450+423_1450+428d others(8): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194272 | ||||||
chr2:162194330
|
AG | A | 15 | a0001c0001t0001g0185a0001c0002t0001g0002a0001c0002t0001g0022others(12): Show | 16 | HG00738.hp1 HG01069.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.1450+370delC | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194330 | ||||||
chr2:162194332
|
G | GA | 6 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0117others(3): Show | 7 | HG00621.hp1 HG01258.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.1450+368dupT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194332 | ||||||
chr2:162194332
|
GA | G | 21 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(18): Show | 26 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1450+368delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194332 | ||||||
chr2:162194349
|
A | T | 1 | a0002c0005t0002g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1450+352T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194349 | ||||||
chr2:162194541
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0089others(1): Show | 4 | HG02970.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450+160T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194541 | ||||||
chr2:162194683
|
A | G | 2 | a0001c0001t0001g0208a0001c0001t0003g0218 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1450+18T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194683 | ||||||
chr2:162194792
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1403-44T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162194792 | ||||||
chr2:162194905
|
C | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(213): Show | 232 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.1403-157G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162194905 | ||||||
chr2:162195133
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1403-385T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195133 | ||||||
chr2:162195194
|
G | C | 23 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0086others(20): Show | 25 | HG00609.hp1 HG00621.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.1403-446C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195194 | ||||||
chr2:162195229
|
A | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0062others(6): Show | 13 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1403-481T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195229 | ||||||
chr2:162195230
|
C | T | 2 | a0002c0005t0002g0215a0002c0005t0002g0216 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1403-482G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195230 | ||||||
chr2:162195419
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1403-671T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195419 | ||||||
chr2:162195429
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1403-681T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195429 | ||||||
chr2:162195515
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0003g0217 | 3 | HG02970.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1403-767G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195515 | ||||||
chr2:162195516
|
G | A | 20 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(17): Show | 24 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1403-768C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195516 | ||||||
chr2:162195539
|
G | A | 2 | a0002c0005t0002g0215a0002c0005t0002g0216 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1403-791C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195539 | ||||||
chr2:162195615
|
T | A | 1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1403-867A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195615 | ||||||
chr2:162195807
|
T | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0117a0001c0001t0001g0139 | 3 | NA18974.hp1 NA19007.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1403-1059A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195807 | ||||||
chr2:162195811
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0210 | 2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1403-1063A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195811 | ||||||
chr2:162195864
|
C | G | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0149 | 3 | HG01358.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1403-1116G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195864 | ||||||
chr2:162195867
|
C | G | 23 | a0001c0001t0001g0059a0001c0001t0001g0076a0001c0001t0001g0085others(20): Show | 23 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1403-1119G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195867 | ||||||
chr2:162195896
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1403-1148A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195896 | ||||||
chr2:162196302
|
G | A | 2 | a0002c0005t0002g0215a0002c0005t0002g0216 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1403-1554C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196302 | ||||||
chr2:162196362
|
A | T | 1 | a0001c0001t0002g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1403-1614T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196362 | ||||||
chr2:162196394
|
T | C | 2 | a0002c0005t0002g0215a0002c0005t0002g0216 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1403-1646A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196394 | ||||||
chr2:162196410
|
C | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1403-1662G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196410 | ||||||
chr2:162196518
|
C | CT | 6 | a0001c0001t0001g0014a0001c0001t0001g0072a0001c0001t0001g0073others(3): Show | 7 | HG02280.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1403-1771dupA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196518 | ||||||
chr2:162196518
|
CT | C | 40 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0083others(37): Show | 44 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1403-1771delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196518 | ||||||
chr2:162196521
|
T | G | 1 | a0001c0002t0001g0047 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1403-1773A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196521 | ||||||
chr2:162196599
|
G | T | 1 | a0001c0001t0001g0113 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1403-1851C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196599 | ||||||
chr2:162196660
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1403-1912G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196660 | ||||||
chr2:162196664
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1403-1916T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196664 | ||||||
chr2:162197072
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1402+1685T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162197072 | ||||||
chr2:162197362
|
T | C | 2 | a0003c0006t0001g0084a0003c0006t0001g0196 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1402+1395A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162197362 | ||||||
chr2:162197373
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1402+1384A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162197373 | ||||||
chr2:162197789
|
A | C | 3 | a0001c0001t0001g0163a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG00639.hp1 HG03654.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1402+968T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162197789 | ||||||
chr2:162197855
|
C | T | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1402+902G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162197855 | ||||||
chr2:162197858
|
A | G | 1 | a0001c0002t0001g0041 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1402+899T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162197858 | ||||||
chr2:162198033
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1402+724A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198033 | ||||||
chr2:162198104
|
G | A | 18 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0021others(15): Show | 20 | HG00621.hp1 HG02015.hp1 HG03654.hp2 others(17): Show |
intron_variant | MODIFIER | c.1402+653C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198104 | ||||||
chr2:162198214
|
C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(65): Show | 76 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.1402+543G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198214 | ||||||
chr2:162198272
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1402+485G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198272 | ||||||
chr2:162198286
|
G | A | 20 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(17): Show | 24 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1402+471C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198286 | ||||||
chr2:162198415
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1402+342C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198415 | ||||||
chr2:162198556
|
ACT | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0192 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1402+199_1402+200d others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198556 | ||||||
chr2:162198558
|
T | G | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1402+199A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198558 | ||||||
chr2:162198684
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0062others(6): Show | 13 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1402+73C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198684 | ||||||
chr2:162199168
|
C | T | 1 | a0001c0002t0001g0032 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1278-287G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199168 | ||||||
chr2:162199222
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0197a0001c0001t0001g0198others(6): Show | 10 | HG02145.hp1 HG02559.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1278-341C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199222 | ||||||
chr2:162199485
|
T | C | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1278-604A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199485 | ||||||
chr2:162199552
|
A | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(8): Show | 15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1278-671T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199552 | ||||||
chr2:162199570
|
C | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0062others(6): Show | 13 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1278-689G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199570 | ||||||
chr2:162199647
|
C | T | 34 | a0001c0001t0001g0166a0001c0002t0001g0002a0001c0002t0001g0003others(31): Show | 37 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.1278-766G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199647 | ||||||
chr2:162199667
|
CA | C | 20 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(17): Show | 24 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1278-787delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199667 | ||||||
chr2:162199788
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1277+778G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199788 | ||||||
chr2:162199803
|
C | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1277+763G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199803 | ||||||
chr2:162199876
|
G | A | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0003g0218 | 3 | HG00140.hp1 HG00741.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1277+690C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199876 | ||||||
chr2:162199877
|
G | C | 1 | a0001c0001t0003g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1277+689C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199877 | ||||||
chr2:162199906
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1277+660C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199906 | ||||||
chr2:162199927
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1277+639T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199927 | ||||||
chr2:162199933
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1277+633T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199933 | ||||||
chr2:162200155
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1277+411C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162200155 | ||||||
chr2:162200255
|
T | A | 1 | a0001c0002t0001g0024 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1277+311A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162200255 | ||||||
chr2:162200393
|
C | T | 20 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(17): Show | 24 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1277+173G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162200393 | ||||||
chr2:162200414
|
T | TTATACTG others(6): Show |
53 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(50): Show | 60 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.1277+151_1277+152i others(15): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162200414 | ||||||
chr2:162200442
|
A | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(67): Show | 79 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.1277+124T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162200442 | ||||||
chr2:162200468
|
G | A | 2 | a0001c0002t0001g0027a0001c0002t0001g0028 | 2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1277+98C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162200468 | ||||||
chr2:162200801
|
A | T | 1 | a0001c0001t0001g0018 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1224-182T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162200801 | ||||||
chr2:162200857
|
G | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1224-238C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162200857 | ||||||
chr2:162201025
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1224-406C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201025 | ||||||
chr2:162201071
|
G | T | 1 | a0001c0001t0001g0111 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1224-452C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201071 | ||||||
chr2:162201241
|
AT | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(8): Show | 15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1224-623delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201241 | ||||||
chr2:162201278
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1224-659C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201278 | ||||||
chr2:162201336
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1224-717T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201336 | ||||||
chr2:162201383
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0164a0001c0007t0001g0052others(1): Show | 5 | HG00733.hp2 HG01175.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1224-764A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201383 | ||||||
chr2:162201387
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1224-768T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201387 | ||||||
chr2:162201493
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1224-874G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201493 | ||||||
chr2:162201504
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1224-885A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201504 | ||||||
chr2:162201638
|
G | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0102 | 2 | NA18977.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1224-1019C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201638 | ||||||
chr2:162202016
|
C | T | 3 | a0002c0005t0001g0061a0002c0005t0002g0215a0002c0005t0002g0216 | 3 | HG02280.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1223+856G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162202016 | ||||||
chr2:162202070
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1223+802A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162202070 | ||||||
chr2:162202083
|
A | T | 1 | a0001c0002t0001g0034 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1223+789T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162202083 | ||||||
chr2:162202298
|
A | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | NA18946.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1223+574T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162202298 | ||||||
chr2:162202314
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1223+558G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162202314 | ||||||
chr2:162202823
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1223+49C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162202823 | ||||||
chr2:162202980
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1153-38G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 13/25 | chr2 | 162202980 | ||||||
chr2:162203235
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1048-90T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162203235 | ||||||
chr2:162203295
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0156 | 2 | HG02155.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1048-150G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162203295 | ||||||
chr2:162203461
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0197a0001c0001t0001g0198others(6): Show | 10 | HG02145.hp1 HG02559.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1048-316C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162203461 | ||||||
chr2:162203528
|
T | A | 1 | a0001c0001t0001g0016 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1048-383A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162203528 | ||||||
chr2:162203717
|
G | A | 3 | a0002c0005t0001g0061a0002c0005t0002g0215a0002c0005t0002g0216 | 3 | HG02280.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1048-572C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162203717 | ||||||
chr2:162204013
|
A | C | 1 | a0001c0001t0001g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1048-868T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204013 | ||||||
chr2:162204017
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1048-872T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204017 | ||||||
chr2:162204084
|
T | C | 1 | a0001c0002t0001g0036 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1048-939A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204084 | ||||||
chr2:162204457
|
G | T | 1 | a0001c0001t0001g0016 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1048-1312C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204457 | ||||||
chr2:162204552
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | NA18946.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1048-1407C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204552 | ||||||
chr2:162204620
|
G | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0089a0001c0001t0001g0136others(1): Show | 4 | HG03139.hp2 HG03453.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048-1475C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204620 | ||||||
chr2:162204914
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1048-1769A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204914 | ||||||
chr2:162204934
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0143 | 3 | HG00735.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1048-1789G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204934 | ||||||
chr2:162205105
|
A | G | 1 | a0001c0002t0001g0033 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1048-1960T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162205105 | ||||||
chr2:162205147
|
T | G | 4 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | HG01168.hp1 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048-2002A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162205147 | ||||||
chr2:162205607
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0169 | 3 | HG02896.hp2 HG02897.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1048-2462C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162205607 | ||||||
chr2:162205790
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1048-2645C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162205790 | ||||||
chr2:162205813
|
A | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1048-2668T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162205813 | ||||||
chr2:162206112
|
T | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0209 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1048-2967A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206112 | ||||||
chr2:162206368
|
G | A | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0004t0001g0007 | 4 | NA18946.hp2 NA18952.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048-3223C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206368 | ||||||
chr2:162206521
|
A | AT | 45 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0083others(42): Show | 49 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1048-3377dupA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206521 | ||||||
chr2:162206592
|
AATAATTG others(21): Show |
A | 1 | a0001c0002t0001g0042 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1047+3332_1047+335 others(32): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206592 | ||||||
chr2:162206669
|
T | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(67): Show | 79 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.1047+3283A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206669 | ||||||
chr2:162206710
|
C | A | 18 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0021others(15): Show | 20 | HG00621.hp1 HG02015.hp1 HG03654.hp2 others(17): Show |
intron_variant | MODIFIER | c.1047+3242G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206710 | ||||||
chr2:162206833
|
G | A | 1 | a0001c0002t0001g0030 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1047+3119C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206833 | ||||||
chr2:162206869
|
C | A | 1 | a0001c0001t0001g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1047+3083G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206869 | ||||||
chr2:162206886
|
A | G | 1 | a0001c0002t0001g0045 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1047+3066T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206886 | ||||||
chr2:162207284
|
T | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(8): Show | 15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1047+2668A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207284 | ||||||
chr2:162207403
|
C | T | 20 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(17): Show | 24 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1047+2549G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207403 | ||||||
chr2:162207714
|
A | AT | 10 | a0001c0001t0001g0076a0001c0001t0001g0152a0001c0001t0001g0190others(7): Show | 10 | HG00558.hp2 HG01891.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1047+2237dupA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207714 | ||||||
chr2:162207714
|
A | ATT | 12 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(9): Show | 16 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1047+2236_1047+223 others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207714 | ||||||
chr2:162207714
|
A | ATTTT | 23 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0021others(20): Show | 25 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1047+2234_1047+223 others(8): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207714 | ||||||
chr2:162207714
|
A | ATTTTT | 5 | a0001c0002t0001g0003a0001c0002t0001g0040a0001c0002t0001g0043others(2): Show | 6 | NA18975.hp2 NA18989.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1047+2233_1047+223 others(9): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207714 | ||||||
chr2:162207753
|
C | G | 1 | a0001c0002t0001g0040 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1047+2199G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207753 | ||||||
chr2:162207811
|
C | T | 3 | a0001c0002t0001g0022a0001c0002t0001g0023a0001c0002t0001g0033 | 3 | HG00738.hp1 HG01928.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1047+2141G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207811 | ||||||
chr2:162207871
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1047+2081G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207871 | ||||||
chr2:162207892
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1047+2060A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207892 | ||||||
chr2:162208122
|
G | A | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1047+1830C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208122 | ||||||
chr2:162208129
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1047+1823C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208129 | ||||||
chr2:162208254
|
TA | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 7 | HG02074.hp1 NA18959.hp2 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.1047+1697delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208254 | ||||||
chr2:162208278
|
C | T | 3 | a0002c0005t0001g0061a0002c0005t0002g0215a0002c0005t0002g0216 | 3 | HG02280.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1047+1674G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208278 | ||||||
chr2:162208438
|
T | C | 1 | a0001c0002t0001g0038 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1047+1514A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208438 | ||||||
chr2:162208471
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1047+1481T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208471 | ||||||
chr2:162208550
|
T | C | 1 | a0001c0002t0001g0021 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1047+1402A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208550 | ||||||
chr2:162208557
|
A | G | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1047+1395T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208557 | ||||||
chr2:162208815
|
A | G | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1047+1137T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208815 | ||||||
chr2:162208824
|
GT | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(19): Show | 26 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1047+1127delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208824 | ||||||
chr2:162209004
|
T | C | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1047+948A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209004 | ||||||
chr2:162209050
|
A | G | 3 | a0001c0001t0001g0201a0003c0006t0001g0084a0003c0006t0001g0196 | 3 | HG02559.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1047+902T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209050 | ||||||
chr2:162209099
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1047+853A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209099 | ||||||
chr2:162209203
|
G | A | 1 | a0001c0001t0003g0217 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1047+749C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209203 | ||||||
chr2:162209363
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(50): Show | 60 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.1047+589C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209363 | ||||||
chr2:162209380
|
A | G | 5 | a0001c0001t0001g0059a0001c0001t0001g0076a0001c0001t0001g0092others(2): Show | 5 | HG02015.hp2 HG02074.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047+572T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209380 | ||||||
chr2:162209490
|
A | C | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1047+462T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209490 | ||||||
chr2:162209577
|
A | AT | 6 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0141others(3): Show | 6 | HG02015.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1047+374dupA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209577 | ||||||
chr2:162209597
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1047+355C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209597 | ||||||
chr2:162209809
|
A | ATCAC | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(8): Show | 15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1047+139_1047+142d others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209809 | ||||||
chr2:162209898
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1047+54G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209898 | ||||||
chr2:162210015
|
C | G | 9 | a0001c0001t0001g0190a0001c0001t0001g0204a0001c0001t0001g0205others(6): Show | 9 | HG01891.hp2 HG02258.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1003-19G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210015 | ||||||
chr2:162210171
|
T | C | 10 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0152others(7): Show | 10 | HG00558.hp2 HG02155.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.1003-175A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210171 | ||||||
chr2:162210184
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1003-188C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210184 | ||||||
chr2:162210281
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(8): Show | 15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1003-285T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210281 | ||||||
chr2:162210578
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1003-582C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210578 | ||||||
chr2:162210808
|
A | C | 1 | a0001c0001t0001g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1003-812T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210808 | ||||||
chr2:162210839
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1003-843C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210839 | ||||||
chr2:162210931
|
A | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1003-935T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210931 | ||||||
chr2:162210947
|
A | T | 15 | a0001c0002t0001g0002a0001c0002t0001g0022a0001c0002t0001g0023others(12): Show | 16 | HG00738.hp1 HG01069.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.1003-951T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210947 | ||||||
chr2:162211046
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1003-1050A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162211046 | ||||||
chr2:162211073
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG00639.hp1 HG02735.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1003-1077C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162211073 | ||||||
chr2:162211641
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1003-1645T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162211641 | ||||||
chr2:162211832
|
C | T | 2 | a0001c0001t0001g0103a0001c0002t0001g0032 | 2 | HG01192.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1003-1836G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162211832 | ||||||
chr2:162211959
|
C | T | 1 | a0001c0002t0001g0031 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1003-1963G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162211959 | ||||||
chr2:162212404
|
T | C | 6 | a0001c0001t0001g0201a0002c0005t0001g0061a0002c0005t0002g0215others(3): Show | 6 | HG02280.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1002+1534A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212404 | ||||||
chr2:162212493
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1002+1445A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212493 | ||||||
chr2:162212538
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1002+1400C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212538 | ||||||
chr2:162212548
|
G | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1002+1390C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212548 | ||||||
chr2:162212642
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1002+1296A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212642 | ||||||
chr2:162212771
|
A | T | 1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1002+1167T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212771 | ||||||
chr2:162212799
|
T | C | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1002+1139A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212799 | ||||||
chr2:162212993
|
G | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1002+945C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212993 | ||||||
chr2:162213054
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1002+884T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213054 | ||||||
chr2:162213350
|
T | C | 1 | a0001c0002t0001g0021 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1002+588A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213350 | ||||||
chr2:162213362
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1002+576C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213362 | ||||||
chr2:162213367
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1002+571C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213367 | ||||||
chr2:162213374
|
C | CA | 12 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0085others(9): Show | 12 | HG01261.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1002+563dupT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213374 | ||||||
chr2:162213404
|
C | CA | 7 | a0001c0001t0001g0013a0001c0001t0001g0070a0001c0001t0001g0197others(4): Show | 8 | HG02145.hp1 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1002+533dupT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213404 | ||||||
chr2:162213424
|
CA | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0083others(14): Show | 18 | HG00609.hp2 HG01192.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1002+513delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213424 | ||||||
chr2:162213428
|
A | C | 40 | a0001c0001t0001g0100a0001c0001t0001g0201a0001c0002t0001g0002others(37): Show | 43 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1002+510T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213428 | ||||||
chr2:162213518
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1002+420G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213518 | ||||||
chr2:162213585
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(8): Show | 15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1002+353G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213585 | ||||||
chr2:162213601
|
A | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(67): Show | 79 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.1002+337T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213601 | ||||||
chr2:162214086
|
T | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.867-13A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162214086 | ||||||
chr2:162214197
|
C | G | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.867-124G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162214197 | ||||||
chr2:162214527
|
G | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.867-454C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162214527 | ||||||
chr2:162214651
|
C | G | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.867-578G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162214651 | ||||||
chr2:162214908
|
G | C | 1 | a0001c0002t0001g0048 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.867-835C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162214908 | ||||||
chr2:162215032
|
TA | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.866+865delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215032 | ||||||
chr2:162215083
|
G | A | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.866+815C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215083 | ||||||
chr2:162215185
|
G | A | 5 | a0001c0001t0001g0059a0001c0001t0001g0076a0001c0001t0001g0092others(2): Show | 5 | HG02015.hp2 HG02074.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.866+713C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215185 | ||||||
chr2:162215216
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(67): Show | 79 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.866+682C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215216 | ||||||
chr2:162215553
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.866+345A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215553 | ||||||
chr2:162215615
|
T | G | 1 | a0001c0001t0001g0015 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.866+283A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215615 | ||||||
chr2:162215706
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.866+192C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215706 | ||||||
chr2:162215721
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0003g0217 | 3 | HG02970.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.866+177C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215721 | ||||||
chr2:162215810
|
C | T | 3 | a0002c0005t0001g0061a0002c0005t0002g0215a0002c0005t0002g0216 | 3 | HG02280.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.866+88G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215810 | ||||||
chr2:162216171
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.763-170C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162216171 | ||||||
chr2:162216318
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.763-317G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162216318 | ||||||
chr2:162216522
|
G | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | NA19007.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.763-521C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162216522 | ||||||
chr2:162216550
|
G | C | 12 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0190others(9): Show | 12 | HG01891.hp2 HG02258.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.763-549C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162216550 | ||||||
chr2:162216561
|
A | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.763-560T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162216561 | ||||||
chr2:162216572
|
T | C | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.763-571A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162216572 | ||||||
chr2:162217212
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(8): Show | 15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.762+774G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162217212 | ||||||
chr2:162217217
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.762+769T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162217217 | ||||||
chr2:162217530
|
T | G | 1 | a0001c0003t0001g0078 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.762+456A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162217530 | ||||||
chr2:162217654
|
G | A | 18 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0021others(15): Show | 20 | HG00621.hp1 HG02015.hp1 HG03654.hp2 others(17): Show |
intron_variant | MODIFIER | c.762+332C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162217654 | ||||||
chr2:162217696
|
A | G | 1 | a0002c0005t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.762+290T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162217696 | ||||||
chr2:162218378
|
T | C | 7 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | HG01168.hp1 HG01192.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.608-238A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218378 | ||||||
chr2:162218450
|
C | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(21): Show | 28 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.608-310G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218450 | ||||||
chr2:162218561
|
T | TTAGA | 29 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0070others(26): Show | 29 | HG00323.hp2 HG00609.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.608-425_608-422dup others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218561 | ||||||
chr2:162218561
|
TTAGA | T | 26 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(23): Show | 30 | HG00733.hp2 HG01175.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.608-425_608-422del others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218561 | ||||||
chr2:162218561
|
TTAGATAG others(1): Show |
T | 19 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0021others(16): Show | 21 | HG00621.hp1 HG01257.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-429_608-422del others(8): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218561 | ||||||
chr2:162218598
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.608-458A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218598 | ||||||
chr2:162218754
|
A | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.607+309T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218754 | ||||||
chr2:162218755
|
T | A | 1 | a0002c0005t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.607+308A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218755 | ||||||
chr2:162219044
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.607+19C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162219044 | ||||||
chr2:162219312
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487-129G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 7/25 | chr2 | 162219312 | ||||||
chr2:162219636
|
T | C | 49 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(46): Show | 54 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.486+217A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 7/25 | chr2 | 162219636 | ||||||
chr2:162220181
|
G | T | 1 | a0001c0001t0001g0097 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.414-256C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162220181 | ||||||
chr2:162220288
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.414-363G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162220288 | ||||||
chr2:162220373
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.414-448G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162220373 | ||||||
chr2:162220830
|
T | G | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.414-905A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162220830 | ||||||
chr2:162221032
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.414-1107T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221032 | ||||||
chr2:162221323
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.414-1398T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221323 | ||||||
chr2:162221330
|
G | C | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.414-1405C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221330 | ||||||
chr2:162221345
|
T | A | 5 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG01168.hp1 HG01346.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.414-1420A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221345 | ||||||
chr2:162221524
|
C | CA | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(44): Show | 55 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.414-1600dupT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221524 | ||||||
chr2:162221685
|
T | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.414-1760A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221685 | ||||||
chr2:162221691
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.414-1766T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221691 | ||||||
chr2:162221793
|
A | G | 2 | a0001c0002t0001g0041a0001c0002t0001g0042 | 2 | NA18941.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.413+1815T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221793 | ||||||
chr2:162222090
|
A | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0062others(6): Show | 13 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+1518T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162222090 | ||||||
chr2:162222146
|
C | T | 5 | a0001c0001t0001g0059a0001c0001t0001g0076a0001c0001t0001g0092others(2): Show | 5 | HG02015.hp2 HG02074.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+1462G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162222146 | ||||||
chr2:162222396
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.413+1212A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162222396 | ||||||
chr2:162222501
|
T | A | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.413+1107A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162222501 | ||||||
chr2:162222508
|
T | A | 1 | a0001c0002t0001g0049 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.413+1100A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162222508 | ||||||
chr2:162222820
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.413+788G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162222820 | ||||||
chr2:162223198
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.413+410G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162223198 | ||||||
chr2:162223307
|
C | T | 13 | a0001c0001t0001g0016a0001c0001t0001g0082a0001c0001t0001g0083others(10): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.413+301G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162223307 | ||||||
chr2:162223582
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.413+26T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162223582 | ||||||
chr2:162223975
|
T | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 233 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.361-315A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 5/25 | chr2 | 162223975 | ||||||
chr2:162224122
|
C | T | 1 | a0001c0002t0001g0021 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.360+344G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 5/25 | chr2 | 162224122 | ||||||
chr2:162224283
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(68): Show | 80 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.360+183T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 5/25 | chr2 | 162224283 | ||||||
chr2:162224578
|
A | T | 1 | a0001c0001t0003g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.286-38T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162224578 | ||||||
chr2:162224718
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.286-178T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162224718 | ||||||
chr2:162224766
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(8): Show | 15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.286-226G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162224766 | ||||||
chr2:162224793
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0089 | 2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.286-253T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162224793 | ||||||
chr2:162224922
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(67): Show | 79 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.286-382G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162224922 | ||||||
chr2:162225260
|
G | A | 5 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0077others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+223C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162225260 | ||||||
chr2:162225321
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.285+162T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162225321 | ||||||
chr2:162225420
|
G | A | 2 | a0002c0005t0001g0061a0002c0005t0002g0215 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.285+63C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162225420 | ||||||
chr2:162225612
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.191-35G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162225612 | ||||||
chr2:162225776
|
G | A | 1 | a0001c0002t0001g0050 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.191-199C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162225776 | ||||||
chr2:162225879
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.191-302T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162225879 | ||||||
chr2:162225885
|
C | A | 49 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(46): Show | 54 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.191-308G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162225885 | ||||||
chr2:162226289
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.190+234A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162226289 | ||||||
chr2:162226370
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.190+153C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162226370 | ||||||
chr2:162226425
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.190+98G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162226425 | ||||||
chr2:162226432
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0197a0001c0001t0001g0198others(5): Show | 9 | HG02145.hp1 HG02559.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.190+91C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162226432 | ||||||
chr2:162226627
|
G | T | 1 | a0001c0001t0001g0005 | 2 | HG00735.hp2 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.92-6C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162226627 | ||||||
chr2:162226640
|
T | C | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-19A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162226640 | ||||||
chr2:162226791
|
C | T | 15 | a0001c0002t0001g0002a0001c0002t0001g0022a0001c0002t0001g0023others(12): Show | 16 | HG00738.hp1 HG01069.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.92-170G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162226791 | ||||||
chr2:162226796
|
T | C | 13 | a0001c0001t0001g0016a0001c0001t0001g0082a0001c0001t0001g0083others(10): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.92-175A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162226796 | ||||||
chr2:162227148
|
C | A | 2 | a0002c0005t0001g0061a0002c0005t0002g0215 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.92-527G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162227148 | ||||||
chr2:162227204
|
T | C | 2 | a0002c0005t0001g0061a0002c0005t0002g0215 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.92-583A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162227204 | ||||||
chr2:162227386
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.92-765T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162227386 | ||||||
chr2:162227970
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(67): Show | 79 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.92-1349G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162227970 | ||||||
chr2:162228488
|
T | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-1867A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162228488 | ||||||
chr2:162228595
|
T | G | 1 | a0002c0005t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92-1974A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162228595 | ||||||
chr2:162228666
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.92-2045A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162228666 | ||||||
chr2:162228914
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.92-2293G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162228914 | ||||||
chr2:162228952
|
G | A | 2 | a0002c0005t0001g0061a0002c0005t0002g0215 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.92-2331C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162228952 | ||||||
chr2:162229381
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.92-2760C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229381 | ||||||
chr2:162229470
|
A | T | 1 | a0001c0001t0001g0163 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.92-2849T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229470 | ||||||
chr2:162229647
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.92-3026G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229647 | ||||||
chr2:162229649
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.92-3028A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229649 | ||||||
chr2:162229770
|
A | G | 1 | a0001c0001t0003g0217 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.92-3149T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229770 | ||||||
chr2:162229838
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.92-3217A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229838 | ||||||
chr2:162229841
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0082a0001c0001t0001g0083others(3): Show | 6 | HG02257.hp1 HG02970.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-3220T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229841 | ||||||
chr2:162229850
|
CAT | C | 20 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 24 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.92-3231_92-3230del others(2): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229850 | ||||||
chr2:162229919
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(68): Show | 80 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.92-3298T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229919 | ||||||
chr2:162230270
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.92-3649A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230270 | ||||||
chr2:162230305
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.92-3684C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230305 | ||||||
chr2:162230563
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.92-3942G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230563 | ||||||
chr2:162230585
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.92-3964G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230585 | ||||||
chr2:162230586
|
G | A | 10 | a0001c0002t0001g0002a0001c0002t0001g0031a0001c0002t0001g0032others(7): Show | 11 | HG01069.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.92-3965C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230586 | ||||||
chr2:162230620
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-3999A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230620 | ||||||
chr2:162230679
|
T | G | 1 | a0001c0001t0001g0172 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.92-4058A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230679 | ||||||
chr2:162230762
|
TG | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-4142delC | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230762 | ||||||
chr2:162230764
|
G | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.92-4143C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230764 | ||||||
chr2:162230915
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(66): Show | 78 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.92-4294G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230915 | ||||||
chr2:162231260
|
T | C | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-4639A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162231260 | ||||||
chr2:162231470
|
C | T | 18 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0021others(15): Show | 20 | HG00621.hp1 HG02015.hp1 HG03654.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-4849G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162231470 | ||||||
chr2:162231644
|
T | C | 1 | a0002c0005t0001g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92-5023A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162231644 | ||||||
chr2:162231769
|
G | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0208a0001c0001t0001g0210 | 3 | HG02647.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.92-5148C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162231769 | ||||||
chr2:162232297
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.92-5676G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162232297 | ||||||
chr2:162232433
|
C | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-5812G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162232433 | ||||||
chr2:162232496
|
G | T | 7 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | HG01168.hp1 HG01192.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-5875C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162232496 | ||||||
chr2:162232704
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-6083G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162232704 | ||||||
chr2:162232705
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.92-6084C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162232705 | ||||||
chr2:162233152
|
A | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0197others(7): Show | 11 | HG02145.hp1 HG02630.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-6531T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162233152 | ||||||
chr2:162233316
|
C | T | 2 | a0001c0001t0001g0016a0004c0008t0001g0017 | 2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.92-6695G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162233316 | ||||||
chr2:162233356
|
C | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-6735G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162233356 | ||||||
chr2:162233401
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.92-6780C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162233401 | ||||||
chr2:162233756
|
C | A | 1 | a0001c0001t0001g0174 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.92-7135G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162233756 | ||||||
chr2:162233916
|
C | A | 1 | a0001c0001t0001g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.92-7295G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162233916 | ||||||
chr2:162234099
|
C | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-7478G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234099 | ||||||
chr2:162234102
|
C | T | 2 | a0001c0002t0001g0003a0001c0002t0001g0040 | 3 | NA19004.hp1 NA19058.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.92-7481G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234102 | ||||||
chr2:162234328
|
A | C | 1 | a0001c0001t0003g0217 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.92-7707T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234328 | ||||||
chr2:162234345
|
G | A | 18 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0021others(15): Show | 20 | HG00621.hp1 HG02015.hp1 HG03654.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-7724C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234345 | ||||||
chr2:162234350
|
C | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | NA18992.hp2 NA18994.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.92-7729G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234350 | ||||||
chr2:162234406
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.92-7785A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234406 | ||||||
chr2:162234460
|
G | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-7839C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234460 | ||||||
chr2:162234467
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG02257.hp2 HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.92-7846A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234467 | ||||||
chr2:162234633
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.92-8012C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234633 | ||||||
chr2:162234674
|
T | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-8053A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234674 | ||||||
chr2:162234787
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.91+8121C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234787 | ||||||
chr2:162234791
|
C | G | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+8117G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234791 | ||||||
chr2:162234816
|
C | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+8092G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234816 | ||||||
chr2:162234881
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.91+8027C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234881 | ||||||
chr2:162234917
|
T | C | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+7991A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234917 | ||||||
chr2:162234938
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.91+7970C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234938 | ||||||
chr2:162235034
|
C | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+7874G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235034 | ||||||
chr2:162235055
|
G | T | 5 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0077others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+7853C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235055 | ||||||
chr2:162235157
|
C | G | 7 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | HG01168.hp1 HG01192.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+7751G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235157 | ||||||
chr2:162235166
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91+7742G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235166 | ||||||
chr2:162235177
|
T | C | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+7731A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235177 | ||||||
chr2:162235243
|
T | C | 61 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(58): Show | 66 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.91+7665A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235243 | ||||||
chr2:162235244
|
T | G | 61 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(58): Show | 66 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.91+7664A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235244 | ||||||
chr2:162235342
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0003g0217 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+7566C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235342 | ||||||
chr2:162235457
|
T | G | 9 | a0001c0001t0001g0013a0001c0001t0001g0197a0001c0001t0001g0198others(6): Show | 10 | HG02145.hp1 HG02630.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+7451A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235457 | ||||||
chr2:162235848
|
T | A | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.91+7060A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235848 | ||||||
chr2:162235974
|
G | A | 2 | a0002c0005t0002g0215a0002c0005t0002g0216 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.91+6934C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235974 | ||||||
chr2:162236036
|
T | C | 4 | a0001c0001t0002g0214a0002c0005t0001g0061a0002c0005t0002g0215others(1): Show | 4 | HG02280.hp1 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+6872A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236036 | ||||||
chr2:162236054
|
T | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0062others(8): Show | 15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.91+6854A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236054 | ||||||
chr2:162236108
|
T | A | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.91+6800A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236108 | ||||||
chr2:162236188
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.91+6720C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236188 | ||||||
chr2:162236303
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+6605G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236303 | ||||||
chr2:162236324
|
A | C | 1 | a0001c0002t0001g0030 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.91+6584T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236324 | ||||||
chr2:162236448
|
G | T | 1 | a0001c0001t0001g0076 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.91+6460C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236448 | ||||||
chr2:162236448
|
GT | G | 32 | a0001c0001t0001g0016a0001c0002t0001g0002a0001c0002t0001g0003others(29): Show | 35 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.91+6459delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236448 | ||||||
chr2:162236496
|
T | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0062others(8): Show | 15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.91+6412A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236496 | ||||||
chr2:162236594
|
A | C | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+6314T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236594 | ||||||
chr2:162236617
|
T | TG | 68 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(65): Show | 77 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.91+6290dupC | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236617 | ||||||
chr2:162236620
|
G | T | 2 | a0001c0003t0001g0074a0001c0003t0001g0075 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.91+6288C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236620 | ||||||
chr2:162236676
|
T | A | 1 | a0001c0001t0001g0179 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.91+6232A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236676 | ||||||
chr2:162236819
|
T | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | HG00609.hp1 NA18946.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.91+6089A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236819 | ||||||
chr2:162236838
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | HG00609.hp1 NA18946.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.91+6070T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236838 | ||||||
chr2:162236862
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0062others(8): Show | 15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.91+6046T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236862 | ||||||
chr2:162237003
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.91+5905A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162237003 | ||||||
chr2:162237171
|
TTGAC | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG02257.hp2 HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.91+5733_91+5736del others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162237171 | ||||||
chr2:162237377
|
G | C | 1 | a0001c0001t0001g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.91+5531C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162237377 | ||||||
chr2:162237663
|
C | A | 7 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | HG01168.hp1 HG01192.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+5245G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162237663 | ||||||
chr2:162237667
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.91+5241A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162237667 | ||||||
chr2:162237883
|
C | T | 4 | a0001c0001t0002g0214a0002c0005t0001g0061a0002c0005t0002g0215others(1): Show | 4 | HG02280.hp1 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+5025G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162237883 | ||||||
chr2:162238045
|
GT | G | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+4862delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238045 | ||||||
chr2:162238047
|
T | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+4861A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238047 | ||||||
chr2:162238131
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.91+4777G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238131 | ||||||
chr2:162238136
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.91+4772T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238136 | ||||||
chr2:162238171
|
TC | T | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG02258.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+4736delG | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238171 | ||||||
chr2:162238398
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.91+4510G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238398 | ||||||
chr2:162238539
|
ATTTC | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+4365_91+4368del others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238539 | ||||||
chr2:162238555
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.91+4353A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238555 | ||||||
chr2:162238769
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | NA18992.hp2 NA18994.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.91+4139G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238769 | ||||||
chr2:162238847
|
A | G | 2 | a0001c0007t0001g0052a0001c0007t0001g0053 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.91+4061T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238847 | ||||||
chr2:162238855
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+4053G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238855 | ||||||
chr2:162238992
|
T | A | 10 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(7): Show | 11 | HG02258.hp2 HG02647.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.91+3916A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238992 | ||||||
chr2:162239040
|
A | G | 2 | a0001c0001t0001g0016a0004c0008t0001g0017 | 2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.91+3868T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162239040 | ||||||
chr2:162239056
|
T | A | 1 | a0001c0001t0001g0189 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.91+3852A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162239056 | ||||||
chr2:162239133
|
C | A | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | HG01891.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.91+3775G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162239133 | ||||||
chr2:162239409
|
C | A | 1 | a0001c0001t0001g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.91+3499G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162239409 | ||||||
chr2:162239502
|
TA | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+3405delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162239502 | ||||||
chr2:162240049
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+2859A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240049 | ||||||
chr2:162240115
|
G | T | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+2793C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240115 | ||||||
chr2:162240269
|
A | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG00621.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.91+2639T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240269 | ||||||
chr2:162240377
|
G | C | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG00639.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.91+2531C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240377 | ||||||
chr2:162240407
|
T | G | 9 | a0001c0001t0001g0013a0001c0001t0001g0197a0001c0001t0001g0198others(6): Show | 10 | HG02145.hp1 HG02630.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+2501A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240407 | ||||||
chr2:162240423
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.91+2485G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240423 | ||||||
chr2:162240424
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02683.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.91+2484C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240424 | ||||||
chr2:162240641
|
C | A | 10 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(7): Show | 11 | HG02258.hp2 HG02647.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.91+2267G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240641 | ||||||
chr2:162240961
|
C | T | 3 | a0001c0002t0001g0022a0001c0002t0001g0023a0001c0002t0001g0024 | 3 | HG00738.hp1 HG01928.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.91+1947G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240961 | ||||||
chr2:162241090
|
G | C | 38 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(35): Show | 41 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.91+1818C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162241090 | ||||||
chr2:162241460
|
G | A | 38 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(35): Show | 41 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.91+1448C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162241460 | ||||||
chr2:162241469
|
C | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(30): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+1439G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162241469 | ||||||
chr2:162241526
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.91+1382G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162241526 | ||||||
chr2:162241635
|
A | G | 38 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(35): Show | 41 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.91+1273T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162241635 | ||||||
chr2:162242045
|
C | T | 1 | a0001c0002t0001g0021 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.91+863G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162242045 | ||||||
chr2:162242185
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+723T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162242185 | ||||||
chr2:162242334
|
A | G | 1 | a0001c0001t0001g0015 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.91+574T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162242334 | ||||||
chr2:162242403
|
T | A | 1 | a0001c0001t0001g0212 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.91+505A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162242403 | ||||||
chr2:162243079
|
T | G | 1 | a0001c0001t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7-87A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 1/25 | chr2 | 162243079 |