Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2254 |
|---|---|
| ensemblid | ENSG00000102678.7 |
| hgncid | 3687 |
| symbol | FGF9 |
| name | fibroblast growth factor 9 |
| refseq_nuc | NM_002010.3 |
| refseq_prot | NP_002001.1 |
| ensembl_nuc | ENST00000382353.6 |
| ensembl_prot | ENSP00000371790.5 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 21671073 |
| end | 21704498 |
| strand | + |
| ver | v1.2 |
| region | chr13:21671073-21704498 |
| region5000 | chr13:21666073-21709498 |
| regionname0 | FGF9_chr13_21671073_21704498 |
| regionname5000 | FGF9_chr13_21666073_21709498 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 208 | 362 | 88 | 70 | 150 | 14 | 38 | 114 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 627 | 295 | 52 | 54 | 147 | 10 | 31 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| c0002 | 1/0 | 627 | 64 | 34 | 15 | 3 | 4 | 7 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| c0003 | 0/0 | 627 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| c0004 | 0/0 | 627 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3904 | 117 | 10 | 26 | 67 | 5 | 8 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0002 | 0/0 | 3906 | 87 | 1 | 16 | 53 | 5 | 12 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0003 | 0/0 | 3908 | 14 | 12 | 2 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0004 | 0/0 | 3910 | 9 | 7 | 0 | 0 | 1 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0005 | 0/0 | 3906 | 6 | 0 | 1 | 2 | 0 | 3 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0006 | 0/0 | 3911 | 6 | 6 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0007 | 0/0 | 3900 | 5 | 0 | 0 | 5 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0008 | 0/0 | 3902 | 5 | 2 | 1 | 1 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0009 | 0/0 | 3912 | 5 | 5 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0010 | 0/0 | 3905 | 5 | 3 | 1 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0011 | 0/0 | 3909 | 5 | 4 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0012 | 0/0 | 3903 | 5 | 0 | 2 | 1 | 0 | 2 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0013 | 0/0 | 3904 | 4 | 4 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0014 | 0/0 | 3915 | 4 | 3 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0015 | 0/0 | 3912 | 4 | 0 | 2 | 0 | 1 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0016 | 0/0 | 3920 | 3 | 2 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0017 | 0/0 | 3905 | 3 | 0 | 0 | 3 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0018 | 0/0 | 3911 | 3 | 1 | 0 | 0 | 1 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0019 | 0/0 | 3906 | 3 | 0 | 0 | 0 | 0 | 3 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0020 | 0/0 | 3906 | 3 | 0 | 1 | 0 | 1 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0021 | 0/0 | 3908 | 3 | 0 | 2 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0022 | 0/0 | 3904 | 2 | 0 | 0 | 1 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0023 | 0/0 | 3904 | 2 | 0 | 0 | 0 | 0 | 2 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0024 | 0/0 | 3908 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0025 | 0/0 | 3908 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0026 | 0/0 | 3904 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0027 | 0/0 | 3907 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0028 | 0/0 | 3907 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0029 | 0/0 | 3909 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0030 | 0/0 | 3901 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0031 | 0/0 | 3906 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0032 | 0/0 | 3907 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0033 | 0/0 | 3909 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0034 | 0/0 | 3906 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0035 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0036 | 0/0 | 3908 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0037 | 0/0 | 3904 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0038 | 0/0 | 3890 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0039 | 0/0 | 3904 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0040 | 0/0 | 3904 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0041 | 0/0 | 3903 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0042 | 0/0 | 3904 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0043 | 0/0 | 3904 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0044 | 0/0 | 3904 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0045 | 0/0 | 3904 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0046 | 0/0 | 3905 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0047 | 0/0 | 3906 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0048 | 0/0 | 3908 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0049 | 0/0 | 3910 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0050 | 0/0 | 3906 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0051 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0052 | 0/0 | 3904 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0053 | 0/0 | 3904 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0054 | 1/0 | 3904 | 1 | 0 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0055 | 0/0 | 3904 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0056 | 0/0 | 3905 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0057 | 0/0 | 3909 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0058 | 0/0 | 3913 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0059 | 0/0 | 3907 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0060 | 0/0 | 3902 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0061 | 0/0 | 3904 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0062 | 0/0 | 3906 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0063 | 0/0 | 3906 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0064 | 0/0 | 3906 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0065 | 0/0 | 3912 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0066 | 0/0 | 3906 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0067 | 0/0 | 3908 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0068 | 0/0 | 3909 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0069 | 0/0 | 3911 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0070 | 0/0 | 3913 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0071 | 0/0 | 3904 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0072 | 0/0 | 3904 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0073 | 0/0 | 3906 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| t0074 | 0/0 | 3904 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 14 | 0 | 1 | 9 | 0 | 4 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0002 | 0/0 | 10 | 0 | 2 | 6 | 0 | 2 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0003 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0004 | 1/0 | 7 | 2 | 3 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0006 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 627 | 295 | 52 | 54 | 147 | 10 | 31 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002 | 1/0 | 627 | 64 | 34 | 15 | 3 | 4 | 7 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0003 | 0/0 | 627 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0004 | 0/0 | 627 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4530 | 110 | 9 | 21 | 67 | 4 | 8 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0002 | 0/0 | 4532 | 87 | 1 | 16 | 53 | 5 | 12 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0003 | 0/0 | 4534 | 13 | 12 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0005 | 0/0 | 4532 | 6 | 0 | 1 | 2 | 0 | 3 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0007 | 0/0 | 4526 | 5 | 0 | 0 | 5 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0008 | 0/0 | 4528 | 5 | 2 | 1 | 1 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0009 | 0/0 | 4538 | 3 | 3 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0010 | 0/0 | 4531 | 5 | 3 | 1 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0011 | 0/0 | 4535 | 5 | 4 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0016 | 0/0 | 4546 | 3 | 2 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0017 | 0/0 | 4531 | 3 | 0 | 0 | 3 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0019 | 0/0 | 4532 | 3 | 0 | 0 | 0 | 0 | 3 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0020 | 0/0 | 4532 | 3 | 0 | 1 | 0 | 1 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0021 | 0/0 | 4534 | 3 | 0 | 2 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0022 | 0/0 | 4530 | 2 | 0 | 0 | 1 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0023 | 0/0 | 4530 | 2 | 0 | 0 | 0 | 0 | 2 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0024 | 0/0 | 4534 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0026 | 0/0 | 4530 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0027 | 0/0 | 4533 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0029 | 0/0 | 4535 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0031 | 0/0 | 4532 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0033 | 0/0 | 4535 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0034 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0036 | 0/0 | 4534 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0037 | 0/0 | 4530 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0038 | 0/0 | 4516 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0039 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0040 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0041 | 0/0 | 4529 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0042 | 0/0 | 4530 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0043 | 0/0 | 4530 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0046 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0048 | 0/0 | 4534 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0049 | 0/0 | 4536 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0052 | 0/0 | 4530 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0053 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0056 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0057 | 0/0 | 4535 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0060 | 0/0 | 4528 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0061 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0062 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0063 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0064 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0065 | 0/0 | 4538 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0066 | 0/0 | 4532 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0068 | 0/0 | 4535 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0071 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0072 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0001t0074 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0001 | 0/0 | 4530 | 6 | 1 | 4 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0003 | 0/0 | 4534 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0004 | 0/0 | 4536 | 9 | 7 | 0 | 0 | 1 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0006 | 0/0 | 4537 | 6 | 6 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0012 | 0/0 | 4529 | 5 | 0 | 2 | 1 | 0 | 2 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0013 | 0/0 | 4530 | 4 | 4 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0014 | 0/0 | 4541 | 4 | 3 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0015 | 0/0 | 4538 | 4 | 0 | 2 | 0 | 1 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0018 | 0/0 | 4537 | 3 | 1 | 0 | 0 | 1 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0024 | 0/0 | 4534 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0025 | 0/0 | 4534 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0028 | 0/0 | 4533 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0030 | 0/0 | 4527 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0032 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0035 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0044 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0045 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0047 | 0/0 | 4532 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0050 | 0/0 | 4532 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0051 | 0/0 | 4526 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0054 | 1/0 | 4530 | 1 | 0 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0055 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0058 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0059 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0067 | 0/0 | 4534 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0069 | 0/0 | 4537 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0070 | 0/0 | 4539 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0002t0073 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0003t0009 | 0/0 | 4538 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| a0001c0004t0001 | 0/0 | 4530 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | copy fasta | chr13 | 21666073 | 21709498 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 1 | 9 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0002 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0003g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0007g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0007g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0008g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0008g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0008g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0009g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0010g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0010g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0010g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0011g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0011g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0011g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0016g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0017g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0017g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0017g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0019g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0019g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0019g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0020g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0020g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0020g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0021g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0021g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0021g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0022g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0022g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0023g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0023g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0024g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0026g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0026g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0027g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0027g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0029g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0029g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0031g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0031g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0033g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0034g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0036g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0037g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0038g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0039g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0040g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0041g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0042g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0043g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0046g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0048g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0049g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0052g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0053g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0056g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0057g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0060g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0061g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0062g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0063g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0064g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0065g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0066g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0068g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0071g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0072g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0074g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0001g0004 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0012g0006 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0013g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0013g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0013g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0014g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0014g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0014g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0015g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0015g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0015g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0018g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0018g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0018g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0024g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0025g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0025g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0028g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0030g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0030g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0032g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0035g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0044g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0045g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0047g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0050g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0051g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0054g0004 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0055g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0058g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0059g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0067g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0069g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0070g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0073g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0003t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0003t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0004t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00099 | hp2 | a0001 | c0002 | t0004 | g0082 | EUR | GBR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00280 | hp1 | a0001 | c0002 | t0015 | g0038 | EUR | FIN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00280 | hp2 | a0001 | c0002 | t0018 | g0197 | EUR | FIN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0228 | EUR | FIN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00323 | hp2 | a0001 | c0001 | t0020 | g0214 | EUR | FIN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00408 | hp1 | a0001 | c0001 | t0007 | g0013 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00438 | hp2 | a0001 | c0001 | t0017 | g0193 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00558 | hp1 | a0001 | c0002 | t0067 | g0230 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00609 | hp1 | a0001 | c0001 | t0007 | g0150 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00639 | hp1 | a0001 | c0002 | t0047 | g0148 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00639 | hp2 | a0001 | c0001 | t0052 | g0126 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0083 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00733 | hp1 | a0001 | c0001 | t0066 | g0203 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00735 | hp1 | a0001 | c0001 | t0016 | g0019 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00738 | hp2 | a0001 | c0002 | t0015 | g0223 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00741 | hp1 | a0001 | c0002 | t0051 | g0065 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01069 | hp2 | a0001 | c0002 | t0069 | g0188 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01070 | hp2 | a0001 | c0002 | t0012 | g0006 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01071 | hp2 | a0001 | c0002 | t0012 | g0006 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01074 | hp2 | a0001 | c0001 | t0026 | g0168 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01081 | hp1 | a0001 | c0001 | t0020 | g0002 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01081 | hp2 | a0001 | c0001 | t0021 | g0034 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01099 | hp1 | a0001 | c0001 | t0010 | g0036 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01099 | hp2 | a0001 | c0002 | t0030 | g0200 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0049 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01243 | hp1 | a0001 | c0002 | t0014 | g0032 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01261 | hp1 | a0001 | c0004 | t0001 | g0033 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01358 | hp1 | a0001 | c0001 | t0042 | g0110 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01361 | hp2 | a0001 | c0002 | t0015 | g0038 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01433 | hp1 | a0001 | c0001 | t0043 | g0171 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0078 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01496 | hp2 | a0001 | c0001 | t0038 | g0003 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0059 | EUR | IBS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0262 | EUR | IBS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0258 | EUR | IBS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0060 | EUR | IBS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0004 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01884 | hp2 | a0001 | c0001 | t0027 | g0063 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01891 | hp1 | a0001 | c0001 | t0029 | g0164 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01891 | hp2 | a0001 | c0001 | t0036 | g0120 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01928 | hp1 | a0001 | c0001 | t0065 | g0226 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01934 | hp2 | a0001 | c0001 | t0037 | g0102 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01975 | hp1 | a0001 | c0002 | t0025 | g0004 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01981 | hp1 | a0001 | c0001 | t0021 | g0209 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0117 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02055 | hp2 | a0001 | c0002 | t0035 | g0169 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02056 | hp2 | a0001 | c0001 | t0071 | g0029 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02071 | hp2 | a0001 | c0001 | t0074 | g0140 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02083 | hp1 | a0001 | c0001 | t0064 | g0249 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02129 | hp1 | a0001 | c0001 | t0022 | g0143 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02132 | hp1 | a0001 | c0002 | t0012 | g0006 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0137 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02145 | hp1 | a0001 | c0002 | t0013 | g0141 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02145 | hp2 | a0001 | c0002 | t0014 | g0032 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02257 | hp1 | a0001 | c0002 | t0058 | g0055 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02257 | hp2 | a0001 | c0001 | t0049 | g0085 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02258 | hp1 | a0001 | c0002 | t0028 | g0031 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02451 | hp1 | a0001 | c0001 | t0016 | g0019 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02451 | hp2 | a0001 | c0002 | t0024 | g0014 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02572 | hp1 | a0001 | c0001 | t0068 | g0187 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0163 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02622 | hp2 | a0001 | c0001 | t0048 | g0147 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02630 | hp1 | a0001 | c0002 | t0006 | g0035 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0050 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02647 | hp1 | a0001 | c0001 | t0041 | g0057 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02683 | hp2 | a0001 | c0002 | t0032 | g0194 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02698 | hp1 | a0001 | c0002 | t0059 | g0196 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02723 | hp1 | a0001 | c0002 | t0004 | g0048 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02723 | hp2 | a0001 | c0002 | t0044 | g0114 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02735 | hp2 | a0001 | c0002 | t0004 | g0184 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02738 | hp1 | a0001 | c0001 | t0019 | g0239 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0062 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02895 | hp1 | a0001 | c0002 | t0018 | g0052 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0183 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0051 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02922 | hp2 | a0001 | c0001 | t0046 | g0130 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02970 | hp1 | a0001 | c0002 | t0014 | g0091 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0081 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02976 | hp2 | a0001 | c0002 | t0006 | g0179 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03041 | hp2 | a0001 | c0002 | t0006 | g0035 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0068 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03130 | hp1 | a0001 | c0002 | t0013 | g0014 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0177 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03139 | hp1 | a0001 | c0002 | t0014 | g0166 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03139 | hp2 | a0001 | c0002 | t0013 | g0014 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03209 | hp2 | a0001 | c0001 | t0056 | g0162 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03225 | hp1 | a0001 | c0002 | t0070 | g0189 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0107 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03239 | hp2 | a0001 | c0001 | t0022 | g0001 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03486 | hp1 | a0001 | c0001 | t0033 | g0118 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0122 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0115 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03490 | hp2 | a0001 | c0002 | t0012 | g0006 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03492 | hp1 | a0001 | c0001 | t0008 | g0001 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03492 | hp2 | a0001 | c0002 | t0012 | g0006 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03516 | hp1 | a0001 | c0002 | t0004 | g0153 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03540 | hp1 | a0001 | c0001 | t0027 | g0181 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03579 | hp2 | a0001 | c0003 | t0009 | g0121 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0123 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0134 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03710 | hp2 | a0001 | c0001 | t0020 | g0232 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03927 | hp2 | a0001 | c0002 | t0018 | g0199 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03942 | hp1 | a0001 | c0001 | t0019 | g0217 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03942 | hp2 | a0001 | c0001 | t0023 | g0185 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | STU | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04115 | hp2 | a0001 | c0001 | t0019 | g0229 | SAS | STU | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04204 | hp1 | a0001 | c0002 | t0015 | g0061 | SAS | STU | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04204 | hp2 | a0001 | c0001 | t0023 | g0001 | SAS | STU | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | STU | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18522 | hp1 | a0001 | c0003 | t0009 | g0011 | AFR | YRI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18522 | hp2 | a0001 | c0002 | t0004 | g0080 | AFR | YRI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | CHB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18612 | hp2 | a0001 | c0002 | t0073 | g0139 | EAS | CHB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18906 | hp1 | a0001 | c0002 | t0025 | g0074 | AFR | YRI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18906 | hp2 | a0001 | c0002 | t0050 | g0072 | AFR | YRI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18944 | hp1 | a0001 | c0001 | t0063 | g0043 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18949 | hp1 | a0001 | c0001 | t0040 | g0093 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18954 | hp2 | a0001 | c0001 | t0007 | g0264 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18960 | hp1 | a0001 | c0001 | t0034 | g0245 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18965 | hp2 | a0001 | c0001 | t0072 | g0132 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18971 | hp1 | a0001 | c0001 | t0021 | g0037 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18972 | hp1 | a0001 | c0001 | t0010 | g0192 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0131 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18988 | hp1 | a0001 | c0001 | t0060 | g0234 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18988 | hp2 | a0001 | c0001 | t0061 | g0256 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19000 | hp2 | a0001 | c0001 | t0017 | g0191 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19006 | hp2 | a0001 | c0001 | t0031 | g0241 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19030 | hp1 | a0001 | c0001 | t0053 | g0113 | AFR | LWK | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19030 | hp2 | a0001 | c0001 | t0024 | g0071 | AFR | LWK | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19043 | hp2 | a0001 | c0001 | t0016 | g0019 | AFR | LWK | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19066 | hp1 | a0001 | c0001 | t0007 | g0112 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19070 | hp2 | a0001 | c0001 | t0062 | g0261 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19074 | hp1 | a0001 | c0001 | t0017 | g0195 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19075 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19083 | hp1 | a0001 | c0001 | t0031 | g0240 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19086 | hp1 | a0001 | c0001 | t0039 | g0159 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20129 | hp1 | a0001 | c0002 | t0055 | g0152 | AFR | ASW | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0036 | AFR | ASW | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | TSI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | TSI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | GIH | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02109 | hp1 | a0001 | c0002 | t0013 | g0135 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0165 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02486 | hp2 | a0001 | c0002 | t0030 | g0198 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02559 | hp1 | a0001 | c0001 | t0057 | g0180 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02559 | hp2 | a0001 | c0002 | t0028 | g0031 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03471 | hp2 | a0001 | c0001 | t0026 | g0161 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | USA | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG06807 | hp2 | a0001 | c0002 | t0045 | g0119 | AFR | USA | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | USA | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20300 | hp2 | a0001 | c0001 | t0029 | g0182 | AFR | USA | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA21309 | hp1 | a0001 | c0002 | t0006 | g0178 | AFR | LWK | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0167 | AFR | LWK | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0109 | REF | REF | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0054 | g0004 | REF | REF | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:21681091
|
C | T | 1 | a0001c0003 | 2 | HG03579.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.327C>T | p.Gly109Gly | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/3 | 1167/4530 | 327/627 | 109/208 | chr13 | 21681091 | ||
| chr13:21701231
|
A | G | 1 | a0001c0004 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.423A>G | p.Glu141Glu | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1263/4530 | 423/627 | 141/208 | chr13 | 21701231 | ||
| chr13:21701255
|
A | G | 3 | a0001c0001a0001c0003a0001c0004 | 298 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(295): Show |
synonymous_variant | LOW | c.447A>G | p.Ser149Ser | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1287/4530 | 447/627 | 149/208 | chr13 | 21701255 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:21671081
|
G | A | 1 | a0001c0002t0032 | 1 | HG02683.hp2 | 5_prime_UTR_variant | MODIFIER | c.-832G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 832 | chr13 | 21671081 | |||||
| chr13:21671104
|
G | C | 1 | a0001c0001t0033 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-809G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 809 | chr13 | 21671104 | |||||
| chr13:21671138
|
G | C | 1 | a0001c0001t0034 | 1 | NA18960.hp1 | 5_prime_UTR_variant | MODIFIER | c.-775G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 775 | chr13 | 21671138 | |||||
| chr13:21671187
|
C | T | 1 | a0001c0001t0074 | 1 | HG02071.hp2 | 5_prime_UTR_variant | MODIFIER | c.-726C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 726 | chr13 | 21671187 | |||||
| chr13:21671201
|
C | T | 2 | a0001c0001t0074a0001c0002t0073 | 2 | HG02071.hp2 NA18612.hp2 |
5_prime_UTR_variant | MODIFIER | c.-712C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 712 | chr13 | 21671201 | |||||
| chr13:21671210
|
C | T | 1 | a0001c0001t0072 | 1 | NA18965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-703C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 703 | chr13 | 21671210 | |||||
| chr13:21671484
|
G | A | 1 | a0001c0002t0035 | 1 | HG02055.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-429G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | chr13 | 21671484 | ||||||
| chr13:21671592
|
G | A | 1 | a0001c0001t0036 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-321G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 321 | chr13 | 21671592 | |||||
| chr13:21671703
|
A | G | 1 | a0001c0001t0071 | 1 | HG02056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-210A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 210 | chr13 | 21671703 | |||||
| chr13:21671742
|
A | G | 3 | a0001c0001t0068a0001c0002t0069a0001c0002t0070 | 3 | HG01069.hp2 HG02572.hp1 HG03225.hp1 |
5_prime_UTR_variant | MODIFIER | c.-171A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 171 | chr13 | 21671742 | |||||
| chr13:21671788
|
C | CT | 19 | a0001c0001t0010a0001c0001t0011a0001c0001t0017others(16): Show | 48 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-117dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 116 | INFO_REALIGN_3_PRIME | chr13 | 21671788 | ||||
| chr13:21671788
|
C | CTT | 15 | a0001c0001t0002a0001c0001t0019a0001c0001t0020others(12): Show | 111 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(108): Show |
5_prime_UTR_variant | MODIFIER | c.-118_-117dupTT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 116 | INFO_REALIGN_3_PRIME | chr13 | 21671788 | ||||
| chr13:21671795
|
T | TC | 3 | a0001c0001t0068a0001c0002t0069a0001c0002t0070 | 3 | HG01069.hp2 HG02572.hp1 HG03225.hp1 |
5_prime_UTR_variant | MODIFIER | c.-118_-117insC | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 117 | chr13 | 21671795 | |||||
| chr13:21701444
|
G | A | 76 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(73): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
3_prime_UTR_variant | MODIFIER | c.*9G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 9 | chr13 | 21701444 | |||||
| chr13:21701458
|
G | A | 1 | a0001c0001t0037 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*23G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 23 | chr13 | 21701458 | |||||
| chr13:21701643
|
G | A | 1 | a0001c0001t0022 | 2 | HG02129.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*208G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 208 | chr13 | 21701643 | |||||
| chr13:21701700
|
A | AGT | 4 | a0001c0002t0032a0001c0002t0059a0001c0002t0067others(1): Show | 4 | HG00558.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*272_*273dupGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 274 | INFO_REALIGN_3_PRIME | chr13 | 21701700 | ||||
| chr13:21701705
|
GTGTA | G | 2 | a0001c0002t0030a0001c0002t0051 | 3 | HG00741.hp1 HG01099.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*274_*277delATGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 274 | INFO_REALIGN_3_PRIME | chr13 | 21701705 | ||||
| chr13:21701707
|
GTA | G | 1 | a0001c0002t0012 | 5 | HG01070.hp2 HG01071.hp2 HG02132.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*274_*275delAT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 274 | INFO_REALIGN_3_PRIME | chr13 | 21701707 | ||||
| chr13:21701709
|
A | ATG | 8 | a0001c0001t0005a0001c0001t0021a0001c0001t0027others(5): Show | 17 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*304_*305dupGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | ||||
| chr13:21701709
|
A | ATGTG | 12 | a0001c0001t0003a0001c0001t0011a0001c0001t0024others(9): Show | 30 | HG00642.hp1 HG01109.hp2 HG01192.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*302_*305dupGTGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | ||||
| chr13:21701709
|
A | ATGTGTG | 7 | a0001c0001t0049a0001c0001t0065a0001c0002t0004others(4): Show | 25 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*300_*305dupGTGTGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | ||||
| chr13:21701709
|
A | ATGTGTGT others(1): Show |
4 | a0001c0001t0009a0001c0002t0058a0001c0002t0070others(1): Show | 7 | HG02257.hp1 HG03225.hp1 HG03225.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*298_*305dupGTGTGT others(2): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | ||||
| chr13:21701709
|
A | ATGTGTGT others(3): Show |
1 | a0001c0002t0014 | 4 | HG01243.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*296_*305dupGTGTGT others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | ||||
| chr13:21701709
|
A | ATGTGTGT others(9): Show |
1 | a0001c0001t0016 | 3 | HG00735.hp1 HG02451.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*290_*305dupGTGTGT others(10): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | ||||
| chr13:21701709
|
A | G | 7 | a0001c0001t0052a0001c0001t0053a0001c0001t0066others(4): Show | 7 | HG00558.hp1 HG00639.hp2 HG00733.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*274A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 274 | chr13 | 21701709 | |||||
| chr13:21701709
|
ATG | A | 2 | a0001c0001t0008a0001c0001t0061 | 6 | HG01496.hp1 HG02109.hp2 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*304_*305delGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 304 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | ||||
| chr13:21701709
|
ATGTG | A | 2 | a0001c0001t0007a0001c0001t0060 | 6 | HG00408.hp1 HG00609.hp1 NA18954.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*302_*305delGTGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 302 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | ||||
| chr13:21701709
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0038 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*292_*305delGTGTGT others(8): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 292 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | ||||
| chr13:21701741
|
A | G | 2 | a0001c0002t0035a0001c0002t0050 | 2 | HG02055.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*306A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | chr13 | 21701741 | |||||
| chr13:21701753
|
G | A | 1 | a0001c0001t0062 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*318G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 318 | chr13 | 21701753 | |||||
| chr13:21701768
|
G | T | 1 | a0001c0001t0064 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*333G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 333 | chr13 | 21701768 | |||||
| chr13:21701786
|
C | T | 3 | a0001c0002t0035a0001c0002t0045a0001c0002t0050 | 3 | HG02055.hp2 HG06807.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*351C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 351 | chr13 | 21701786 | |||||
| chr13:21701807
|
A | T | 30 | a0001c0001t0029a0001c0001t0036a0001c0001t0048others(27): Show | 62 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*372A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 372 | chr13 | 21701807 | |||||
| chr13:21701877
|
T | C | 1 | a0001c0002t0059 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 442 | chr13 | 21701877 | |||||
| chr13:21701918
|
C | T | 3 | a0001c0002t0035a0001c0002t0045a0001c0002t0050 | 3 | HG02055.hp2 HG06807.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*483C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 483 | chr13 | 21701918 | |||||
| chr13:21701931
|
C | T | 2 | a0001c0001t0020a0001c0001t0043 | 4 | HG00323.hp2 HG01081.hp1 HG01433.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*496C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 496 | chr13 | 21701931 | |||||
| chr13:21701976
|
C | A | 1 | a0001c0001t0031 | 2 | NA19006.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*541C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 541 | chr13 | 21701976 | |||||
| chr13:21702001
|
T | A | 1 | a0001c0001t0060 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*566T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 566 | chr13 | 21702001 | |||||
| chr13:21702304
|
C | T | 1 | a0001c0001t0042 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*869C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 869 | chr13 | 21702304 | |||||
| chr13:21702431
|
A | G | 3 | a0001c0001t0036a0001c0001t0048a0001c0001t0053 | 3 | HG01891.hp2 HG02622.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*996A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 996 | chr13 | 21702431 | |||||
| chr13:21702529
|
C | T | 37 | a0001c0001t0016a0001c0001t0024a0001c0001t0026others(34): Show | 72 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1094C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1094 | chr13 | 21702529 | |||||
| chr13:21702701
|
A | G | 1 | a0001c0001t0049 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1266A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1266 | chr13 | 21702701 | |||||
| chr13:21702827
|
T | A | 3 | a0001c0002t0035a0001c0002t0045a0001c0002t0050 | 3 | HG02055.hp2 HG06807.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1392T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1392 | chr13 | 21702827 | |||||
| chr13:21702828
|
C | T | 3 | a0001c0002t0035a0001c0002t0045a0001c0002t0050 | 3 | HG02055.hp2 HG06807.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1393C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1393 | chr13 | 21702828 | |||||
| chr13:21702846
|
T | C | 1 | a0001c0001t0039 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1411T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1411 | chr13 | 21702846 | |||||
| chr13:21702953
|
A | G | 1 | a0001c0001t0033 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1518A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1518 | chr13 | 21702953 | |||||
| chr13:21702972
|
A | G | 1 | a0001c0002t0044 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1537A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1537 | chr13 | 21702972 | |||||
| chr13:21703059
|
T | C | 1 | a0001c0001t0056 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1624T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1624 | chr13 | 21703059 | |||||
| chr13:21703106
|
A | G | 1 | a0001c0001t0063 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1671A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1671 | chr13 | 21703106 | |||||
| chr13:21703760
|
A | G | 2 | a0001c0001t0017a0001c0001t0040 | 4 | HG00438.hp2 NA18949.hp1 NA19000.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2325A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 2325 | chr13 | 21703760 | |||||
| chr13:21703930
|
AT | A | 3 | a0001c0001t0026a0001c0001t0041a0001c0001t0046 | 4 | HG01074.hp2 HG02647.hp1 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2497delT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 2497 | INFO_REALIGN_3_PRIME | chr13 | 21703930 | ||||
| chr13:21703998
|
G | C | 33 | a0001c0001t0016a0001c0001t0024a0001c0001t0029others(30): Show | 67 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2563G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 2563 | chr13 | 21703998 | |||||
| chr13:21704020
|
C | T | 3 | a0001c0001t0016a0001c0001t0029a0001c0002t0006 | 11 | HG00735.hp1 HG01891.hp1 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2585C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 2585 | chr13 | 21704020 | |||||
| chr13:21704069
|
C | T | 2 | a0001c0001t0019a0001c0001t0023 | 5 | HG02738.hp1 HG03942.hp1 HG03942.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2634C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 2634 | chr13 | 21704069 | |||||
| chr13:21704372
|
G | A | 1 | a0001c0002t0044 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2937G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 2937 | chr13 | 21704372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:21672318
|
GTCTC | G | 1 | a0001c0001t0016g0019 | 3 | HG00735.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.277+141_277+144del others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21672318 | |||||
| chr13:21672322
|
C | G | 1 | a0001c0001t0007g0264 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.277+133C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672322 | ||||||
| chr13:21672505
|
C | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0045 | 3 | HG00423.hp1 NA18950.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.277+316C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672505 | ||||||
| chr13:21672580
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.277+391G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672580 | ||||||
| chr13:21672581
|
C | A | 1 | a0001c0001t0001g0046 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.277+392C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672581 | ||||||
| chr13:21672598
|
C | A | 1 | a0001c0001t0001g0046 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.277+409C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672598 | ||||||
| chr13:21672650
|
G | T | 81 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(78): Show | 105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.277+461G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672650 | ||||||
| chr13:21672875
|
A | C | 11 | a0001c0001t0010g0192a0001c0001t0017g0191a0001c0001t0017g0193others(8): Show | 15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+686A>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672875 | ||||||
| chr13:21672902
|
T | A | 11 | a0001c0001t0010g0192a0001c0001t0017g0191a0001c0001t0017g0193others(8): Show | 15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+713T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672902 | ||||||
| chr13:21672903
|
G | C | 11 | a0001c0001t0010g0192a0001c0001t0017g0191a0001c0001t0017g0193others(8): Show | 15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+714G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672903 | ||||||
| chr13:21673107
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.277+918A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673107 | ||||||
| chr13:21673656
|
C | T | 3 | a0001c0001t0068g0187a0001c0002t0069g0188a0001c0002t0070g0189 | 3 | HG01069.hp2 HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.277+1467C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673656 | ||||||
| chr13:21673689
|
G | A | 1 | a0001c0001t0005g0047 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.277+1500G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673689 | ||||||
| chr13:21673698
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.277+1509C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673698 | ||||||
| chr13:21673746
|
G | A | 1 | a0001c0002t0004g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.277+1557G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673746 | ||||||
| chr13:21673800
|
GCCAGGCG others(70): Show |
G | 1 | a0001c0001t0023g0185 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.277+1613_277+1689d others(79): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21673800 | |||||
| chr13:21673855
|
G | T | 1 | a0001c0001t0010g0036 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.277+1666G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673855 | ||||||
| chr13:21673928
|
C | T | 1 | a0001c0002t0004g0184 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.277+1739C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673928 | ||||||
| chr13:21673979
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.277+1790C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673979 | ||||||
| chr13:21674330
|
G | C | 4 | a0001c0001t0011g0049a0001c0001t0011g0050a0001c0001t0011g0051others(1): Show | 4 | HG01109.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+2141G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674330 | ||||||
| chr13:21674428
|
G | A | 2 | a0001c0001t0003g0053a0001c0001t0003g0054 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.277+2239G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674428 | ||||||
| chr13:21674432
|
G | C | 1 | a0001c0001t0002g0201 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.277+2243G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674432 | ||||||
| chr13:21674505
|
G | C | 4 | a0001c0001t0068g0187a0001c0002t0058g0055a0001c0002t0069g0188others(1): Show | 4 | HG01069.hp2 HG02257.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+2316G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674505 | ||||||
| chr13:21674515
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.277+2326G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674515 | ||||||
| chr13:21674527
|
G | C | 1 | a0001c0001t0041g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.277+2338G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674527 | ||||||
| chr13:21674562
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.277+2373G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674562 | ||||||
| chr13:21674589
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0021g0037 | 2 | NA18948.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.277+2400G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674589 | ||||||
| chr13:21674594
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.277+2405T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674594 | ||||||
| chr13:21674707
|
A | AT | 15 | a0001c0001t0002g0262a0001c0001t0011g0183a0001c0001t0027g0181others(12): Show | 20 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.277+2530dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21674707 | |||||
| chr13:21674802
|
G | A | 3 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0002t0015g0061 | 3 | HG01515.hp1 HG01517.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.277+2613G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674802 | ||||||
| chr13:21674909
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.277+2720A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674909 | ||||||
| chr13:21674914
|
A | G | 1 | a0001c0001t0011g0183 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.277+2725A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674914 | ||||||
| chr13:21674940
|
G | A | 2 | a0001c0001t0010g0062a0001c0001t0027g0063 | 2 | HG01884.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.277+2751G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674940 | ||||||
| chr13:21675005
|
C | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(232): Show | 304 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(301): Show |
intron_variant | MODIFIER | c.277+2816C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675005 | ||||||
| chr13:21675046
|
A | T | 2 | a0001c0001t0010g0062a0001c0001t0027g0063 | 2 | HG01884.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.277+2857A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675046 | ||||||
| chr13:21675115
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.277+2926G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675115 | ||||||
| chr13:21675145
|
C | A | 1 | a0001c0001t0066g0203 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.277+2956C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675145 | ||||||
| chr13:21675239
|
A | T | 1 | a0001c0001t0003g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.277+3050A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675239 | ||||||
| chr13:21675410
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 6 | NA18956.hp2 NA18998.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+3221C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675410 | ||||||
| chr13:21675451
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0092a0001c0001t0008g0007others(1): Show | 6 | HG00438.hp1 HG02523.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+3262G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675451 | ||||||
| chr13:21675648
|
A | G | 2 | a0001c0001t0002g0258a0001c0001t0002g0259 | 2 | HG01517.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.277+3459A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675648 | ||||||
| chr13:21675836
|
A | G | 124 | a0001c0001t0001g0033a0001c0001t0001g0172a0001c0001t0002g0002others(121): Show | 155 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.277+3647A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675836 | ||||||
| chr13:21675924
|
C | CT | 10 | a0001c0001t0001g0089a0001c0001t0001g0160a0001c0001t0001g0172others(7): Show | 11 | HG00558.hp2 HG01167.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.277+3750dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21675924 | |||||
| chr13:21675924
|
CT | C | 21 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0002g0059others(18): Show | 24 | HG01074.hp2 HG01243.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.277+3750delT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21675924 | |||||
| chr13:21675939
|
T | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0094a0001c0001t0001g0095others(13): Show | 22 | HG01256.hp2 HG01361.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.277+3750T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675939 | ||||||
| chr13:21675970
|
T | C | 1 | a0001c0001t0002g0205 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.277+3781T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675970 | ||||||
| chr13:21676050
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0155others(4): Show | 10 | HG00423.hp2 HG02083.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.277+3861A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21676050 | ||||||
| chr13:21676177
|
G | C | 1 | a0001c0001t0002g0208 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.277+3988G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21676177 | ||||||
| chr13:21676524
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.277+4335T>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21676524 | ||||||
| chr13:21676645
|
C | G | 1 | a0001c0001t0002g0254 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.278-4397C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21676645 | ||||||
| chr13:21676659
|
G | A | 1 | a0001c0001t0011g0049 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.278-4383G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21676659 | ||||||
| chr13:21677244
|
A | C | 84 | a0001c0001t0001g0172a0001c0001t0002g0002a0001c0001t0002g0009others(81): Show | 107 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.278-3798A>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21677244 | ||||||
| chr13:21677664
|
A | G | 1 | a0001c0001t0043g0171 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.278-3378A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21677664 | ||||||
| chr13:21677668
|
C | A | 1 | a0001c0001t0009g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.278-3374C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21677668 | ||||||
| chr13:21678023
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.278-3019C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678023 | ||||||
| chr13:21678116
|
A | G | 2 | a0001c0001t0002g0043a0001c0001t0063g0043 | 2 | NA18944.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.278-2926A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678116 | ||||||
| chr13:21678170
|
A | T | 1 | a0001c0001t0001g0154 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.278-2872A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678170 | ||||||
| chr13:21678339
|
C | T | 1 | a0001c0001t0026g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.278-2703C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678339 | ||||||
| chr13:21678565
|
G | C | 6 | a0001c0001t0010g0192a0001c0001t0017g0191a0001c0001t0017g0193others(3): Show | 6 | HG00438.hp2 HG02683.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.278-2477G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678565 | ||||||
| chr13:21678572
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.278-2470T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678572 | ||||||
| chr13:21678846
|
A | C | 4 | a0001c0001t0010g0167a0001c0002t0006g0177a0001c0002t0006g0178others(1): Show | 4 | HG02976.hp2 HG03130.hp2 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-2196A>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678846 | ||||||
| chr13:21678980
|
G | A | 1 | a0001c0001t0021g0209 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.278-2062G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678980 | ||||||
| chr13:21678991
|
C | G | 19 | a0001c0001t0011g0050a0001c0001t0011g0051a0001c0001t0011g0165others(16): Show | 22 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.278-2051C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678991 | ||||||
| chr13:21679016
|
G | T | 8 | a0001c0001t0002g0009a0001c0001t0002g0037a0001c0001t0002g0250others(5): Show | 11 | HG00544.hp2 HG01346.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-2026G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679016 | ||||||
| chr13:21679278
|
C | T | 5 | a0001c0001t0011g0183a0001c0001t0027g0181a0001c0001t0029g0182others(2): Show | 6 | HG02559.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-1764C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679278 | ||||||
| chr13:21679533
|
A | C | 3 | a0001c0001t0011g0050a0001c0001t0011g0051a0001c0002t0018g0052 | 3 | HG02630.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.278-1509A>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679533 | ||||||
| chr13:21679600
|
T | C | 2 | a0001c0001t0010g0062a0001c0001t0027g0063 | 2 | HG01884.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.278-1442T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679600 | ||||||
| chr13:21679674
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.278-1368C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679674 | ||||||
| chr13:21679721
|
G | T | 20 | a0001c0001t0001g0172a0001c0001t0002g0041a0001c0001t0002g0042others(17): Show | 23 | HG00408.hp2 HG00558.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.278-1321G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679721 | ||||||
| chr13:21679742
|
T | C | 80 | a0001c0001t0001g0172a0001c0001t0002g0002a0001c0001t0002g0009others(77): Show | 103 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.278-1300T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679742 | ||||||
| chr13:21679754
|
C | T | 1 | a0001c0002t0004g0153 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.278-1288C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679754 | ||||||
| chr13:21679755
|
A | G | 1 | a0001c0002t0004g0153 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.278-1287A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679755 | ||||||
| chr13:21679782
|
C | CA | 22 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(19): Show | 25 | HG00280.hp2 HG00741.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.278-1239dupA | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21679782 | |||||
| chr13:21679782
|
CA | C | 25 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0151others(22): Show | 33 | HG01074.hp1 HG01099.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.278-1239delA | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21679782 | |||||
| chr13:21679804
|
T | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0109 | 3 | HG01069.hp1 HG01071.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.278-1238T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679804 | ||||||
| chr13:21679813
|
G | A | 2 | a0001c0001t0053g0113a0001c0002t0044g0114 | 2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.278-1229G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679813 | ||||||
| chr13:21679818
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.278-1224G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679818 | ||||||
| chr13:21679853
|
A | T | 1 | a0001c0002t0070g0189 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.278-1189A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679853 | ||||||
| chr13:21679956
|
C | CA | 35 | a0001c0001t0001g0069a0001c0001t0001g0116a0001c0001t0001g0155others(32): Show | 43 | HG00423.hp2 HG01070.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.278-1064dupA | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21679956 | |||||
| chr13:21679956
|
CA | C | 21 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0046others(18): Show | 23 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.278-1064delA | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21679956 | |||||
| chr13:21680151
|
C | T | 26 | a0001c0001t0003g0088a0001c0001t0005g0047a0001c0001t0010g0036others(23): Show | 30 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.278-891C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680151 | ||||||
| chr13:21680447
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0003g0175 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.278-595G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680447 | ||||||
| chr13:21680452
|
C | CT | 17 | a0001c0001t0002g0259a0001c0001t0009g0107a0001c0001t0010g0192others(14): Show | 21 | HG00280.hp2 HG00438.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.278-576dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21680452 | |||||
| chr13:21680458
|
T | C | 1 | a0001c0001t0002g0212 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.278-584T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680458 | ||||||
| chr13:21680469
|
T | C | 1 | a0001c0002t0006g0177 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.278-573T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680469 | ||||||
| chr13:21680526
|
A | C | 1 | a0001c0001t0002g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.278-516A>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680526 | ||||||
| chr13:21680766
|
A | G | 83 | a0001c0001t0001g0172a0001c0001t0002g0002a0001c0001t0002g0009others(80): Show | 106 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.278-276A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680766 | ||||||
| chr13:21680873
|
A | G | 1 | a0001c0001t0002g0253 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.278-169A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680873 | ||||||
| chr13:21681014
|
T | C | 20 | a0001c0001t0003g0088a0001c0001t0010g0036a0001c0001t0010g0062others(17): Show | 24 | HG01074.hp2 HG01099.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.278-28T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21681014 | ||||||
| chr13:21681028
|
C | T | 78 | a0001c0001t0001g0172a0001c0001t0002g0002a0001c0001t0002g0009others(75): Show | 101 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.278-14C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21681028 | ||||||
| chr13:21681162
|
C | T | 82 | a0001c0001t0001g0172a0001c0001t0002g0002a0001c0001t0002g0009others(79): Show | 105 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.381+17C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21681162 | ||||||
| chr13:21681261
|
T | C | 20 | a0001c0001t0003g0088a0001c0001t0010g0036a0001c0001t0010g0062others(17): Show | 24 | HG01074.hp2 HG01099.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.381+116T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21681261 | ||||||
| chr13:21681284
|
G | A | 1 | a0001c0002t0058g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.381+139G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21681284 | ||||||
| chr13:21681811
|
G | A | 14 | a0001c0001t0003g0088a0001c0001t0011g0165a0001c0001t0011g0183others(11): Show | 17 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.381+666G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21681811 | ||||||
| chr13:21682029
|
G | C | 1 | a0001c0001t0060g0234 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.381+884G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682029 | ||||||
| chr13:21682035
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.381+890G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682035 | ||||||
| chr13:21682082
|
C | T | 1 | a0001c0002t0055g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.381+937C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682082 | ||||||
| chr13:21682438
|
A | G | 77 | a0001c0001t0001g0172a0001c0001t0002g0002a0001c0001t0002g0009others(74): Show | 100 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.381+1293A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682438 | ||||||
| chr13:21682486
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.381+1341A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682486 | ||||||
| chr13:21682551
|
A | G | 2 | a0001c0001t0007g0112a0001c0001t0039g0159 | 2 | NA19066.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.381+1406A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682551 | ||||||
| chr13:21682582
|
A | G | 83 | a0001c0001t0001g0172a0001c0001t0002g0002a0001c0001t0002g0009others(80): Show | 106 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.381+1437A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682582 | ||||||
| chr13:21682694
|
G | GT | 83 | a0001c0001t0001g0094a0001c0001t0001g0144a0001c0001t0001g0145others(80): Show | 106 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.381+1566dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21682694 | |||||
| chr13:21682694
|
G | GTT | 10 | a0001c0001t0002g0210a0001c0001t0002g0211a0001c0001t0002g0233others(7): Show | 10 | HG00544.hp2 HG01928.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+1565_381+1566d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21682694 | |||||
| chr13:21682701
|
T | G | 17 | a0001c0001t0003g0088a0001c0001t0011g0050a0001c0001t0011g0051others(14): Show | 20 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.381+1556T>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682701 | ||||||
| chr13:21682861
|
A | G | 1 | a0001c0002t0030g0200 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.381+1716A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682861 | ||||||
| chr13:21683014
|
T | C | 1 | a0001c0002t0001g0070 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.381+1869T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683014 | ||||||
| chr13:21683152
|
C | T | 1 | a0001c0002t0035g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.381+2007C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683152 | ||||||
| chr13:21683219
|
A | G | 1 | a0001c0001t0003g0142 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.381+2074A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683219 | ||||||
| chr13:21683287
|
C | T | 1 | a0001c0001t0002g0259 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.381+2142C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683287 | ||||||
| chr13:21683347
|
G | A | 8 | a0001c0001t0003g0011a0001c0001t0009g0011a0001c0001t0009g0107others(5): Show | 10 | HG00735.hp1 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+2202G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683347 | ||||||
| chr13:21683655
|
A | G | 114 | a0001c0001t0001g0145a0001c0001t0001g0172a0001c0001t0001g0174others(111): Show | 142 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.381+2510A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683655 | ||||||
| chr13:21683905
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.381+2760G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683905 | ||||||
| chr13:21684069
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.381+2924C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684069 | ||||||
| chr13:21684182
|
C | A | 1 | a0001c0001t0010g0036 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.381+3037C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684182 | ||||||
| chr13:21684206
|
T | C | 2 | a0001c0001t0053g0113a0001c0002t0044g0114 | 2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.381+3061T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684206 | ||||||
| chr13:21684295
|
T | C | 1 | a0001c0001t0010g0036 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.381+3150T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684295 | ||||||
| chr13:21684444
|
T | C | 2 | a0001c0001t0005g0115a0001c0001t0005g0123 | 2 | HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.381+3299T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684444 | ||||||
| chr13:21684476
|
G | A | 4 | a0001c0001t0001g0058a0001c0001t0001g0108a0001c0001t0001g0124others(1): Show | 4 | HG02523.hp2 NA18952.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+3331G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684476 | ||||||
| chr13:21684490
|
T | G | 1 | a0001c0001t0010g0036 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.381+3345T>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684490 | ||||||
| chr13:21684540
|
T | C | 1 | a0001c0001t0010g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.381+3395T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684540 | ||||||
| chr13:21684575
|
G | GGT | 3 | a0001c0001t0068g0187a0001c0002t0069g0188a0001c0002t0070g0189 | 3 | HG01069.hp2 HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.381+3438_381+3439d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21684575 | |||||
| chr13:21684636
|
G | A | 99 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0002g0002others(96): Show | 127 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.381+3491G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684636 | ||||||
| chr13:21684820
|
T | C | 3 | a0001c0001t0017g0191a0001c0001t0017g0193a0001c0001t0017g0195 | 3 | HG00438.hp2 NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.381+3675T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684820 | ||||||
| chr13:21685228
|
C | T | 18 | a0001c0001t0003g0088a0001c0001t0010g0036a0001c0001t0011g0165others(15): Show | 21 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.381+4083C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685228 | ||||||
| chr13:21685233
|
C | T | 15 | a0001c0001t0003g0088a0001c0001t0010g0036a0001c0001t0011g0165others(12): Show | 18 | HG00639.hp1 HG01099.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.381+4088C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685233 | ||||||
| chr13:21685271
|
C | T | 114 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0002g0002others(111): Show | 146 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.381+4126C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685271 | ||||||
| chr13:21685272
|
G | A | 112 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0002g0002others(109): Show | 144 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.381+4127G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685272 | ||||||
| chr13:21685312
|
T | C | 1 | a0001c0002t0035g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.381+4167T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685312 | ||||||
| chr13:21685373
|
G | A | 2 | a0001c0001t0036g0120a0001c0001t0048g0147 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.381+4228G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685373 | ||||||
| chr13:21685502
|
A | G | 112 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0002g0002others(109): Show | 144 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.381+4357A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685502 | ||||||
| chr13:21685596
|
C | T | 2 | a0001c0001t0002g0225a0001c0002t0014g0166 | 2 | HG03139.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.381+4451C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685596 | ||||||
| chr13:21685862
|
C | T | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.381+4717C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685862 | ||||||
| chr13:21686060
|
T | C | 11 | a0001c0001t0010g0192a0001c0001t0017g0191a0001c0001t0017g0193others(8): Show | 15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+4915T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686060 | ||||||
| chr13:21686345
|
A | C | 1 | a0001c0001t0026g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.381+5200A>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686345 | ||||||
| chr13:21686493
|
T | C | 2 | a0001c0001t0002g0041a0001c0001t0002g0243 | 3 | HG01167.hp1 HG01169.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.381+5348T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686493 | ||||||
| chr13:21686518
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.381+5373G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686518 | ||||||
| chr13:21686541
|
C | G | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.381+5396C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686541 | ||||||
| chr13:21686620
|
T | A | 99 | a0001c0001t0001g0012a0001c0001t0001g0145a0001c0001t0001g0172others(96): Show | 129 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.381+5475T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686620 | ||||||
| chr13:21686621
|
C | A | 88 | a0001c0001t0001g0012a0001c0001t0001g0145a0001c0001t0001g0172others(85): Show | 114 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.381+5476C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686621 | ||||||
| chr13:21686696
|
A | G | 97 | a0001c0001t0001g0012a0001c0001t0001g0145a0001c0001t0001g0172others(94): Show | 126 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.381+5551A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686696 | ||||||
| chr13:21686762
|
G | A | 9 | a0001c0001t0003g0011a0001c0001t0009g0011a0001c0001t0009g0107others(6): Show | 11 | HG00735.hp1 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.381+5617G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686762 | ||||||
| chr13:21687256
|
C | T | 1 | a0001c0001t0010g0036 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.381+6111C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687256 | ||||||
| chr13:21687493
|
T | C | 1 | a0001c0002t0004g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.381+6348T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687493 | ||||||
| chr13:21687528
|
A | G | 11 | a0001c0001t0010g0192a0001c0001t0017g0191a0001c0001t0017g0193others(8): Show | 15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+6383A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687528 | ||||||
| chr13:21687670
|
G | C | 2 | a0001c0001t0036g0120a0001c0001t0048g0147 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.381+6525G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687670 | ||||||
| chr13:21687865
|
G | A | 10 | a0001c0001t0001g0125a0001c0001t0003g0088a0001c0001t0011g0183others(7): Show | 11 | HG00639.hp1 HG01891.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.381+6720G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687865 | ||||||
| chr13:21687904
|
A | G | 1 | a0001c0002t0015g0061 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.381+6759A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687904 | ||||||
| chr13:21687979
|
A | G | 1 | a0001c0001t0027g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.381+6834A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687979 | ||||||
| chr13:21687988
|
C | T | 1 | a0001c0002t0058g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.381+6843C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687988 | ||||||
| chr13:21688051
|
G | A | 2 | a0001c0001t0053g0113a0001c0002t0044g0114 | 2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.381+6906G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688051 | ||||||
| chr13:21688092
|
C | T | 81 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0002g0002others(78): Show | 106 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.381+6947C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688092 | ||||||
| chr13:21688385
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.381+7240G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688385 | ||||||
| chr13:21688448
|
C | T | 1 | a0001c0002t0047g0148 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.381+7303C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688448 | ||||||
| chr13:21688451
|
T | C | 1 | a0001c0001t0041g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.381+7306T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688451 | ||||||
| chr13:21688554
|
T | C | 90 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0002g0002others(87): Show | 115 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.381+7409T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688554 | ||||||
| chr13:21688752
|
A | AT | 17 | a0001c0001t0001g0029a0001c0001t0002g0009a0001c0001t0002g0016others(14): Show | 22 | HG01069.hp2 HG01346.hp1 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.381+7623dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21688752 | |||||
| chr13:21688752
|
A | ATT | 72 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0002g0002others(69): Show | 92 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.381+7622_381+7623d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21688752 | |||||
| chr13:21688752
|
AT | A | 11 | a0001c0001t0008g0023a0001c0001t0011g0051a0001c0001t0017g0191others(8): Show | 12 | HG00438.hp2 HG01074.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.381+7623delT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21688752 | |||||
| chr13:21688872
|
G | T | 4 | a0001c0001t0002g0246a0001c0001t0002g0247a0001c0001t0002g0248others(1): Show | 4 | HG00408.hp2 NA18956.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+7727G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688872 | ||||||
| chr13:21688894
|
A | T | 1 | a0001c0001t0002g0204 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.381+7749A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688894 | ||||||
| chr13:21688964
|
G | T | 2 | a0001c0001t0049g0085a0001c0002t0035g0169 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.381+7819G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688964 | ||||||
| chr13:21689016
|
A | G | 1 | a0001c0002t0006g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.381+7871A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689016 | ||||||
| chr13:21689060
|
G | A | 7 | a0001c0001t0011g0165a0001c0001t0029g0164a0001c0001t0049g0085others(4): Show | 8 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+7915G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689060 | ||||||
| chr13:21689076
|
A | G | 1 | a0001c0001t0064g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.381+7931A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689076 | ||||||
| chr13:21689083
|
G | A | 4 | a0001c0001t0024g0071a0001c0001t0027g0181a0001c0001t0057g0180others(1): Show | 4 | HG02559.hp1 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+7938G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689083 | ||||||
| chr13:21689158
|
T | C | 1 | a0001c0001t0002g0244 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.381+8013T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689158 | ||||||
| chr13:21689315
|
G | A | 2 | a0001c0001t0001g0073a0001c0002t0025g0074 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.381+8170G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689315 | ||||||
| chr13:21689346
|
C | G | 97 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0002g0002others(94): Show | 126 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.381+8201C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689346 | ||||||
| chr13:21689372
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.381+8227A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689372 | ||||||
| chr13:21689375
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.381+8230C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689375 | ||||||
| chr13:21689448
|
CT | C | 82 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0002g0002others(79): Show | 107 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.381+8315delT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21689448 | |||||
| chr13:21689467
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.381+8322A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689467 | ||||||
| chr13:21689736
|
T | C | 82 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0002g0002others(79): Show | 107 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.381+8591T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689736 | ||||||
| chr13:21689811
|
T | C | 81 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0002g0002others(78): Show | 106 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.381+8666T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689811 | ||||||
| chr13:21689885
|
C | T | 2 | a0001c0001t0049g0085a0001c0002t0035g0169 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.381+8740C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689885 | ||||||
| chr13:21689886
|
G | A | 1 | a0001c0001t0010g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.381+8741G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689886 | ||||||
| chr13:21690151
|
A | G | 1 | a0001c0001t0005g0137 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.381+9006A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690151 | ||||||
| chr13:21690223
|
C | T | 84 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0002g0002others(81): Show | 109 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.381+9078C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690223 | ||||||
| chr13:21690631
|
T | C | 11 | a0001c0001t0010g0192a0001c0001t0017g0191a0001c0001t0017g0193others(8): Show | 15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+9486T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690631 | ||||||
| chr13:21690714
|
C | T | 17 | a0001c0001t0001g0125a0001c0001t0003g0088a0001c0001t0011g0165others(14): Show | 19 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.381+9569C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690714 | ||||||
| chr13:21690728
|
G | A | 1 | a0001c0001t0020g0214 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.381+9583G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690728 | ||||||
| chr13:21690776
|
C | T | 2 | a0001c0001t0036g0120a0001c0001t0048g0147 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.381+9631C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690776 | ||||||
| chr13:21690870
|
G | A | 11 | a0001c0001t0010g0192a0001c0001t0017g0191a0001c0001t0017g0193others(8): Show | 15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+9725G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690870 | ||||||
| chr13:21690872
|
T | C | 2 | a0001c0001t0049g0085a0001c0002t0035g0169 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.381+9727T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690872 | ||||||
| chr13:21690964
|
T | G | 13 | a0001c0001t0010g0192a0001c0001t0017g0191a0001c0001t0017g0193others(10): Show | 17 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.381+9819T>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690964 | ||||||
| chr13:21690979
|
A | G | 11 | a0001c0001t0010g0192a0001c0001t0017g0191a0001c0001t0017g0193others(8): Show | 15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+9834A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690979 | ||||||
| chr13:21691382
|
A | T | 78 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0002g0002others(75): Show | 103 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.382-9808A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691382 | ||||||
| chr13:21691594
|
A | T | 5 | a0001c0001t0002g0034a0001c0001t0002g0059a0001c0001t0002g0060others(2): Show | 5 | HG00323.hp1 HG01081.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-9596A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691594 | ||||||
| chr13:21691596
|
C | A | 1 | a0001c0002t0035g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.382-9594C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691596 | ||||||
| chr13:21691620
|
C | G | 1 | a0001c0001t0001g0172 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.382-9570C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691620 | ||||||
| chr13:21691710
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.382-9480C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691710 | ||||||
| chr13:21691897
|
T | C | 8 | a0001c0001t0001g0125a0001c0001t0003g0088a0001c0001t0011g0183others(5): Show | 11 | HG00639.hp1 HG00735.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.382-9293T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691897 | ||||||
| chr13:21691923
|
T | A | 1 | a0001c0001t0042g0110 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.382-9267T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691923 | ||||||
| chr13:21691979
|
C | CT | 139 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0015others(136): Show | 181 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.382-9197dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21691979 | |||||
| chr13:21691979
|
CT | C | 18 | a0001c0001t0001g0075a0001c0001t0011g0050a0001c0001t0011g0051others(15): Show | 23 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.382-9197delT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21691979 | |||||
| chr13:21692095
|
A | G | 2 | a0001c0001t0066g0203a0001c0002t0015g0223 | 2 | HG00733.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.382-9095A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692095 | ||||||
| chr13:21692492
|
C | G | 1 | a0001c0001t0005g0133 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.382-8698C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692492 | ||||||
| chr13:21692577
|
A | G | 3 | a0001c0001t0036g0120a0001c0001t0053g0113a0001c0002t0006g0179 | 3 | HG01891.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.382-8613A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692577 | ||||||
| chr13:21692679
|
C | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0015others(70): Show | 102 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.382-8511C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692679 | ||||||
| chr13:21692750
|
C | T | 2 | a0001c0001t0005g0133a0001c0001t0005g0137 | 2 | HG02135.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.382-8440C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692750 | ||||||
| chr13:21692791
|
G | A | 3 | a0001c0001t0003g0088a0001c0001t0010g0036a0001c0001t0011g0183 | 4 | HG01099.hp1 HG02895.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-8399G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692791 | ||||||
| chr13:21692792
|
A | T | 1 | a0001c0001t0029g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.382-8398A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692792 | ||||||
| chr13:21692871
|
A | T | 1 | a0001c0002t0015g0223 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.382-8319A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692871 | ||||||
| chr13:21692998
|
C | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(221): Show | 292 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(289): Show |
intron_variant | MODIFIER | c.382-8192C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692998 | ||||||
| chr13:21693130
|
A | G | 1 | a0001c0001t0002g0262 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.382-8060A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693130 | ||||||
| chr13:21693177
|
A | G | 1 | a0001c0002t0055g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.382-8013A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693177 | ||||||
| chr13:21693198
|
G | A | 1 | a0001c0001t0002g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.382-7992G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693198 | ||||||
| chr13:21693267
|
T | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(241): Show | 317 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.382-7923T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693267 | ||||||
| chr13:21693408
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.382-7782C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693408 | ||||||
| chr13:21693519
|
C | G | 5 | a0001c0001t0003g0142a0001c0002t0013g0014a0001c0002t0013g0135others(2): Show | 6 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-7671C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693519 | ||||||
| chr13:21693624
|
T | C | 5 | a0001c0001t0003g0142a0001c0002t0013g0014a0001c0002t0013g0135others(2): Show | 6 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-7566T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693624 | ||||||
| chr13:21693864
|
G | A | 4 | a0001c0002t0035g0169a0001c0002t0044g0114a0001c0002t0045g0119others(1): Show | 4 | HG02055.hp2 HG02723.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-7326G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693864 | ||||||
| chr13:21694140
|
G | A | 3 | a0001c0001t0036g0120a0001c0001t0048g0147a0001c0001t0053g0113 | 3 | HG01891.hp2 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.382-7050G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21694140 | ||||||
| chr13:21694364
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.382-6826A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21694364 | ||||||
| chr13:21694487
|
C | A | 15 | a0001c0001t0036g0120a0001c0001t0048g0147a0001c0001t0053g0113others(12): Show | 17 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.382-6703C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21694487 | ||||||
| chr13:21694507
|
C | T | 72 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(69): Show | 101 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.382-6683C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21694507 | ||||||
| chr13:21695069
|
C | CGT | 3 | a0001c0001t0003g0054a0001c0001t0026g0161a0001c0001t0026g0168 | 3 | HG01074.hp2 HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.382-6109_382-6108d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695069 | |||||
| chr13:21695069
|
CGTGTGTG others(11): Show |
C | 3 | a0001c0002t0014g0032a0001c0002t0014g0091a0001c0002t0014g0166 | 4 | HG01243.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-6107_382-6090d others(20): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695069 | |||||
| chr13:21695083
|
C | CGT | 42 | a0001c0001t0001g0003a0001c0001t0001g0056a0001c0001t0001g0084others(39): Show | 52 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.382-6075_382-6074d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695083 | |||||
| chr13:21695083
|
C | CGTGT | 4 | a0001c0001t0001g0075a0001c0001t0001g0094a0001c0001t0002g0207others(1): Show | 4 | HG00099.hp1 HG01884.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-6077_382-6074d others(6): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695083 | |||||
| chr13:21695083
|
C | T | 17 | a0001c0001t0003g0010a0001c0001t0003g0025a0001c0001t0003g0053others(14): Show | 21 | HG01099.hp1 HG01109.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.382-6107C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695083 | ||||||
| chr13:21695083
|
CGT | C | 11 | a0001c0001t0001g0067a0001c0001t0001g0108a0001c0001t0002g0246others(8): Show | 11 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.382-6075_382-6074d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695083 | |||||
| chr13:21695083
|
CGTGTGTG others(1): Show |
C | 4 | a0001c0002t0013g0014a0001c0002t0013g0135a0001c0002t0013g0141others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-6081_382-6074d others(10): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695083 | |||||
| chr13:21695083
|
CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0001g0174a0001c0001t0002g0260 | 2 | NA18956.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.382-6087_382-6074d others(16): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695083 | |||||
| chr13:21695085
|
T | C | 17 | a0001c0001t0003g0010a0001c0001t0003g0025a0001c0001t0003g0053others(14): Show | 21 | HG01099.hp1 HG01109.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.382-6105T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695085 | ||||||
| chr13:21695087
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.382-6103T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695087 | ||||||
| chr13:21695113
|
T | A | 4 | a0001c0001t0026g0161a0001c0001t0026g0168a0001c0001t0036g0120others(1): Show | 4 | HG01074.hp2 HG01891.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-6077T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695113 | ||||||
| chr13:21695115
|
T | A | 23 | a0001c0001t0003g0010a0001c0001t0003g0025a0001c0001t0003g0053others(20): Show | 27 | HG01074.hp2 HG01099.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.382-6075T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695115 | ||||||
| chr13:21695170
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0073 | 2 | HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.382-6020G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695170 | ||||||
| chr13:21695316
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(226): Show | 297 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(294): Show |
intron_variant | MODIFIER | c.382-5874T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695316 | ||||||
| chr13:21695490
|
G | T | 19 | a0001c0001t0003g0010a0001c0001t0003g0025a0001c0001t0003g0053others(16): Show | 23 | HG01074.hp2 HG01099.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.382-5700G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695490 | ||||||
| chr13:21695528
|
G | C | 8 | a0001c0002t0012g0006a0001c0002t0030g0198a0001c0002t0030g0200others(5): Show | 12 | HG00558.hp1 HG00741.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.382-5662G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695528 | ||||||
| chr13:21695653
|
C | G | 1 | a0001c0002t0070g0189 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.382-5537C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695653 | ||||||
| chr13:21695765
|
T | C | 2 | a0001c0001t0002g0210a0001c0001t0002g0225 | 2 | NA18971.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.382-5425T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695765 | ||||||
| chr13:21695850
|
G | A | 2 | a0001c0001t0003g0025a0001c0001t0003g0090 | 3 | HG02922.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.382-5340G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695850 | ||||||
| chr13:21695896
|
C | T | 1 | a0001c0002t0055g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.382-5294C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695896 | ||||||
| chr13:21695988
|
C | T | 4 | a0001c0002t0035g0169a0001c0002t0044g0114a0001c0002t0045g0119others(1): Show | 4 | HG02055.hp2 HG02723.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-5202C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695988 | ||||||
| chr13:21696000
|
C | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0077a0001c0001t0001g0186others(3): Show | 7 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.382-5190C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696000 | ||||||
| chr13:21696329
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(202): Show | 269 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.382-4861C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696329 | ||||||
| chr13:21696333
|
A | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(227): Show | 298 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.382-4857A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696333 | ||||||
| chr13:21696547
|
C | CAT | 267 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(264): Show | 343 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(340): Show |
intron_variant | MODIFIER | c.382-4643_382-4642i others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696547 | ||||||
| chr13:21696554
|
G | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(248): Show | 325 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.382-4636G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696554 | ||||||
| chr13:21696646
|
T | G | 1 | a0001c0001t0016g0019 | 3 | HG00735.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.382-4544T>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696646 | ||||||
| chr13:21696649
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(99): Show | 132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.382-4541A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696649 | ||||||
| chr13:21696996
|
T | C | 1 | a0001c0003t0009g0121 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.382-4194T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696996 | ||||||
| chr13:21697232
|
A | AC | 3 | a0001c0001t0017g0191a0001c0001t0017g0193a0001c0001t0017g0195 | 3 | HG00438.hp2 NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.382-3957dupC | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21697232 | |||||
| chr13:21697426
|
C | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(223): Show | 294 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.382-3764C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697426 | ||||||
| chr13:21697498
|
G | A | 1 | a0001c0002t0055g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.382-3692G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697498 | ||||||
| chr13:21697517
|
A | G | 21 | a0001c0001t0003g0010a0001c0001t0003g0025a0001c0001t0003g0053others(18): Show | 25 | HG01074.hp2 HG01099.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.382-3673A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697517 | ||||||
| chr13:21697580
|
C | A | 1 | a0001c0002t0069g0188 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.382-3610C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697580 | ||||||
| chr13:21697625
|
G | GTATA | 7 | a0001c0001t0003g0053a0001c0001t0003g0054a0001c0001t0003g0066others(4): Show | 8 | HG01099.hp1 HG02615.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-3564_382-3561d others(6): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21697625 | |||||
| chr13:21697691
|
C | A | 1 | a0001c0001t0005g0047 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.382-3499C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697691 | ||||||
| chr13:21697766
|
G | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0129a0001c0001t0042g0110 | 3 | HG00738.hp1 HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.382-3424G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697766 | ||||||
| chr13:21697808
|
C | CT | 20 | a0001c0001t0001g0125a0001c0001t0001g0173a0001c0001t0002g0222others(17): Show | 22 | HG00639.hp1 HG01069.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.382-3366dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21697808 | |||||
| chr13:21697869
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(247): Show | 324 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.382-3321C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697869 | ||||||
| chr13:21697933
|
G | T | 2 | a0001c0002t0025g0074a0001c0002t0058g0055 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.382-3257G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697933 | ||||||
| chr13:21697939
|
C | A | 2 | a0001c0002t0025g0074a0001c0002t0058g0055 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.382-3251C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697939 | ||||||
| chr13:21697958
|
C | T | 1 | a0001c0002t0070g0189 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.382-3232C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697958 | ||||||
| chr13:21698133
|
C | T | 1 | a0001c0001t0021g0209 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.382-3057C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698133 | ||||||
| chr13:21698228
|
A | G | 4 | a0001c0001t0002g0039a0001c0001t0002g0212a0001c0001t0002g0218others(1): Show | 5 | NA18995.hp1 NA19012.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-2962A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698228 | ||||||
| chr13:21698260
|
G | A | 1 | a0001c0002t0004g0082 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.382-2930G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698260 | ||||||
| chr13:21698368
|
G | A | 1 | a0001c0001t0056g0162 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.382-2822G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698368 | ||||||
| chr13:21698594
|
C | G | 4 | a0001c0002t0013g0014a0001c0002t0013g0135a0001c0002t0013g0141others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-2596C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698594 | ||||||
| chr13:21698744
|
A | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0146 | 2 | NA18945.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.382-2446A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698744 | ||||||
| chr13:21698768
|
G | A | 2 | a0001c0001t0011g0049a0001c0001t0068g0187 | 2 | HG01109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.382-2422G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698768 | ||||||
| chr13:21698943
|
G | A | 3 | a0001c0002t0014g0032a0001c0002t0014g0091a0001c0002t0014g0166 | 4 | HG01243.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-2247G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698943 | ||||||
| chr13:21699026
|
A | G | 4 | a0001c0002t0013g0014a0001c0002t0013g0135a0001c0002t0013g0141others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-2164A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699026 | ||||||
| chr13:21699151
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(202): Show | 269 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.382-2039C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699151 | ||||||
| chr13:21699369
|
C | T | 4 | a0001c0002t0035g0169a0001c0002t0044g0114a0001c0002t0045g0119others(1): Show | 4 | HG02055.hp2 HG02723.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-1821C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699369 | ||||||
| chr13:21699396
|
C | T | 1 | a0001c0002t0004g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.382-1794C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699396 | ||||||
| chr13:21699444
|
A | G | 1 | a0001c0001t0002g0251 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.382-1746A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699444 | ||||||
| chr13:21699765
|
C | T | 3 | a0001c0002t0014g0032a0001c0002t0014g0091a0001c0002t0014g0166 | 4 | HG01243.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-1425C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699765 | ||||||
| chr13:21699933
|
T | A | 2 | a0001c0002t0025g0074a0001c0002t0058g0055 | 2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.382-1257T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699933 | ||||||
| chr13:21699993
|
C | T | 8 | a0001c0002t0012g0006a0001c0002t0030g0198a0001c0002t0030g0200others(5): Show | 12 | HG00558.hp1 HG00741.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.382-1197C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699993 | ||||||
| chr13:21700015
|
G | GGT | 8 | a0001c0002t0003g0083a0001c0002t0004g0080a0001c0002t0004g0153others(5): Show | 12 | HG00558.hp1 HG00642.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-1142_382-1141d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21700015 | |||||
| chr13:21700015
|
G | GGTGTGTG others(1): Show |
3 | a0001c0002t0032g0194a0001c0002t0058g0055a0001c0002t0059g0196 | 3 | HG02257.hp1 HG02683.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.382-1148_382-1141d others(10): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21700015 | |||||
| chr13:21700015
|
GGT | G | 26 | a0001c0001t0001g0075a0001c0001t0001g0089a0001c0001t0001g0099others(23): Show | 30 | HG00099.hp1 HG00673.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.382-1142_382-1141d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21700015 | |||||
| chr13:21700015
|
GGTGT | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(209): Show | 278 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.382-1144_382-1141d others(6): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21700015 | |||||
| chr13:21700177
|
G | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(248): Show | 325 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.382-1013G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700177 | ||||||
| chr13:21700187
|
C | G | 1 | a0001c0001t0001g0144 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.382-1003C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700187 | ||||||
| chr13:21700250
|
G | C | 1 | a0001c0001t0002g0221 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.382-940G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700250 | ||||||
| chr13:21700303
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(99): Show | 132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.382-887T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700303 | ||||||
| chr13:21700623
|
A | G | 1 | a0001c0002t0055g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.382-567A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700623 | ||||||
| chr13:21700701
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.382-489A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700701 | ||||||
| chr13:21700836
|
T | C | 1 | a0001c0001t0046g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.382-354T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700836 | ||||||
| chr13:21700857
|
A | G | 1 | a0001c0001t0056g0162 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.382-333A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700857 | ||||||
| chr13:21700946
|
G | A | 3 | a0001c0002t0014g0032a0001c0002t0014g0091a0001c0002t0014g0166 | 4 | HG01243.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-244G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700946 | ||||||
| chr13:21700988
|
A | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(249): Show | 326 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.382-202A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700988 | ||||||
| chr13:21701054
|
T | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(249): Show | 326 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.382-136T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21701054 | ||||||
| chr13:21701071
|
T | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(249): Show | 326 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.382-119T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21701071 |