Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 54902 |
|---|---|
| ensemblid | ENSG00000011295.16 |
| hgncid | 26006 |
| symbol | TTC19 |
| name | tetratricopeptide repeat domain 19 |
| refseq_nuc | NM_017775.4 |
| refseq_prot | NP_060245.3 |
| ensembl_nuc | ENST00000261647.10 |
| ensembl_prot | ENSP00000261647.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 15999824 |
| end | 16029404 |
| strand | + |
| ver | v1.2 |
| region | chr17:15999824-16029404 |
| region5000 | chr17:15994824-16034404 |
| regionname0 | TTC19_chr17_15999824_16029404 |
| regionname5000 | TTC19_chr17_15994824_16034404 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 380 | 322 | 92 | 67 | 116 | 12 | 33 | 90 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0002 | 0/0 | 380 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0003 | 0/0 | 380 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0004 | 0/0 | 380 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0005 | 0/0 | 380 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1143 | 304 | 76 | 65 | 116 | 12 | 33 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| c0002 | 0/0 | 1143 | 14 | 13 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| c0003 | 0/0 | 1143 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| c0004 | 0/0 | 1143 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| c0005 | 0/0 | 1143 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| c0006 | 0/0 | 1143 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| c0007 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| c0008 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| c0009 | 0/0 | 1143 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1908 | 95 | 13 | 18 | 49 | 5 | 8 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0002 | 0/0 | 1909 | 25 | 1 | 5 | 9 | 0 | 10 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0003 | 0/0 | 1907 | 25 | 9 | 4 | 10 | 0 | 2 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0004 | 0/0 | 1918 | 23 | 0 | 9 | 6 | 4 | 4 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0005 | 0/0 | 1920 | 15 | 3 | 2 | 10 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0006 | 0/0 | 1912 | 12 | 5 | 3 | 4 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0007 | 0/0 | 1919 | 10 | 1 | 2 | 4 | 1 | 2 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0008 | 0/0 | 1921 | 8 | 1 | 1 | 6 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0009 | 0/0 | 1919 | 6 | 6 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0010 | 0/0 | 1903 | 6 | 5 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0011 | 0/0 | 1911 | 5 | 5 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0012 | 0/0 | 1924 | 5 | 0 | 4 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0013 | 0/0 | 1920 | 4 | 0 | 2 | 0 | 0 | 2 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0014 | 0/0 | 1917 | 4 | 0 | 0 | 2 | 1 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0015 | 0/0 | 1902 | 4 | 1 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0016 | 0/0 | 1913 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0017 | 0/0 | 1913 | 3 | 1 | 1 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0018 | 0/0 | 1912 | 3 | 0 | 1 | 0 | 1 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0019 | 0/0 | 1911 | 3 | 1 | 1 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0020 | 0/0 | 1911 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0021 | 0/0 | 1923 | 3 | 0 | 1 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0022 | 0/0 | 1918 | 3 | 0 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0023 | 0/0 | 1910 | 3 | 0 | 1 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0024 | 0/0 | 1918 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0025 | 0/0 | 1917 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0026 | 0/0 | 1910 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0027 | 0/0 | 1910 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0028 | 0/0 | 1902 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0029 | 0/0 | 1910 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0030 | 0/0 | 1932 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0031 | 0/0 | 1913 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0032 | 0/0 | 1919 | 2 | 1 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0033 | 0/0 | 1910 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0034 | 0/0 | 1925 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0035 | 0/0 | 1922 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0036 | 0/0 | 1921 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0037 | 0/0 | 1918 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0038 | 0/0 | 1917 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0039 | 0/0 | 1913 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0040 | 0/0 | 1911 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0041 | 0/0 | 1910 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0042 | 0/0 | 1910 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0043 | 0/0 | 1900 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0044 | 0/0 | 1910 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0045 | 0/0 | 1908 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0046 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0047 | 0/0 | 1909 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0048 | 0/0 | 1910 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0049 | 0/0 | 1910 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0050 | 0/0 | 1909 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0051 | 0/0 | 1908 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0052 | 0/0 | 1933 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0053 | 0/0 | 1922 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0054 | 0/0 | 1921 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0055 | 0/0 | 1921 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0056 | 0/0 | 1910 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0057 | 0/0 | 1911 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0058 | 0/0 | 1910 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0059 | 0/0 | 1912 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0060 | 0/0 | 1895 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0061 | 0/0 | 1922 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0062 | 0/0 | 1919 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0063 | 0/0 | 1913 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0064 | 0/0 | 1910 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0065 | 0/0 | 1909 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0066 | 0/0 | 1899 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0067 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0068 | 0/0 | 1908 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0069 | 0/0 | 1919 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| t0070 | 0/0 | 1908 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 34 | 7 | 8 | 9 | 3 | 7 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0002 | 0/0 | 12 | 0 | 6 | 2 | 1 | 3 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0004 | 0/0 | 8 | 1 | 3 | 4 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0007 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0010 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0011 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0012 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0014 | 0/0 | 4 | 2 | 0 | 1 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0015 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0018 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0021 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0041 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1143 | 304 | 76 | 65 | 116 | 12 | 33 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0002 | 0/0 | 1143 | 14 | 13 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0004 | 0/0 | 1143 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0007 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0009 | 0/0 | 1143 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0002c0003 | 0/0 | 1143 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0003c0008 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0004c0005 | 0/0 | 1143 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0005c0006 | 0/0 | 1143 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3050 | 93 | 11 | 18 | 49 | 5 | 8 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0002 | 0/0 | 3051 | 25 | 1 | 5 | 9 | 0 | 10 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0003 | 0/0 | 3049 | 25 | 9 | 4 | 10 | 0 | 2 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0004 | 0/0 | 3060 | 22 | 0 | 9 | 6 | 4 | 3 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0005 | 0/0 | 3062 | 15 | 3 | 2 | 10 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0006 | 0/0 | 3054 | 12 | 5 | 3 | 4 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0007 | 0/0 | 3061 | 10 | 1 | 2 | 4 | 1 | 2 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0008 | 0/0 | 3063 | 8 | 1 | 1 | 6 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0010 | 0/0 | 3045 | 5 | 4 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0011 | 0/0 | 3053 | 5 | 5 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0012 | 0/0 | 3066 | 5 | 0 | 4 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0013 | 0/0 | 3062 | 4 | 0 | 2 | 0 | 0 | 2 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0014 | 0/0 | 3059 | 4 | 0 | 0 | 2 | 1 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0015 | 0/0 | 3044 | 4 | 1 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0016 | 0/0 | 3055 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0017 | 0/0 | 3055 | 3 | 1 | 1 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0018 | 0/0 | 3054 | 3 | 0 | 1 | 0 | 1 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0019 | 0/0 | 3053 | 3 | 1 | 1 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0020 | 0/0 | 3053 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0021 | 0/0 | 3065 | 3 | 0 | 1 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0022 | 0/0 | 3060 | 3 | 0 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0023 | 0/0 | 3052 | 3 | 0 | 1 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0027 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0028 | 0/0 | 3044 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0029 | 0/0 | 3052 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0030 | 0/0 | 3074 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0031 | 0/0 | 3055 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0032 | 0/0 | 3061 | 2 | 1 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0033 | 0/0 | 3052 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0037 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0038 | 0/0 | 3059 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0039 | 0/0 | 3055 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0040 | 0/0 | 3053 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0041 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0042 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0043 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0044 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0045 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0046 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0047 | 0/0 | 3051 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0048 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0049 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0050 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0051 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0052 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0053 | 0/0 | 3064 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0054 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0055 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0057 | 0/0 | 3053 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0058 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0059 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0060 | 0/0 | 3037 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0062 | 0/0 | 3061 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0063 | 0/0 | 3055 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0065 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0066 | 0/0 | 3041 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0067 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0068 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0069 | 0/0 | 3061 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0001t0070 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0002t0009 | 0/0 | 3061 | 6 | 6 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0002t0024 | 0/0 | 3060 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0002t0025 | 0/0 | 3059 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0002t0026 | 0/0 | 3052 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0002t0034 | 0/0 | 3067 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0002t0036 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0004t0010 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0004t0028 | 0/0 | 3044 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0007t0027 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0001c0009t0061 | 0/0 | 3064 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0002c0003t0001 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0002c0003t0056 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0002c0003t0064 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0003c0008t0001 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0004c0005t0004 | 0/0 | 3060 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| a0005c0006t0035 | 0/0 | 3064 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | copy fasta | chr17 | 15994824 | 16034404 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 6 | 3 | 7 | 3 | 4 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0004 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0014 | 0/0 | 4 | 2 | 0 | 1 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0041 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0001 | 0/0 | 7 | 1 | 2 | 1 | 0 | 3 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0008g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0008g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0008g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0010g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0010g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0010g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0011g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0011g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0012g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0012g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0012g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0012g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0013g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0013g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0014g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0014g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0014g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0014g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0015g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0015g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0015g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0016g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0016g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0017g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0017g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0017g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0018g0010 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0019g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0019g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0019g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0020g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0021g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0021g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0021g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0022g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0022g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0022g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0023g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0023g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0023g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0027g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0028g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0029g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0030g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0030g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0031g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0031g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0032g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0032g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0033g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0033g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0037g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0038g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0039g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0040g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0041g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0042g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0043g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0044g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0045g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0046g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0047g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0048g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0049g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0050g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0051g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0052g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0053g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0054g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0055g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0057g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0058g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0059g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0060g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0062g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0063g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0065g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0066g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0067g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0068g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0069g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0070g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0009g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0024g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0024g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0025g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0025g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0026g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0026g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0034g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0036g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0004t0010g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0004t0028g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0007t0027g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0009t0061g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0002c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0002c0003t0056g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0002c0003t0064g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0003c0008t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0004c0005t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0005c0006t0035g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | FIN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00323 | hp2 | a0001 | c0001 | t0018 | g0010 | EUR | FIN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00408 | hp1 | a0001 | c0001 | t0022 | g0072 | EAS | CHS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | CHS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00639 | hp2 | a0001 | c0001 | t0052 | g0061 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0082 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0086 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01069 | hp1 | a0001 | c0001 | t0013 | g0027 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01071 | hp1 | a0001 | c0001 | t0013 | g0027 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01106 | hp1 | a0001 | c0001 | t0018 | g0010 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01109 | hp1 | a0001 | c0001 | t0053 | g0059 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01109 | hp2 | a0005 | c0006 | t0035 | g0184 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01168 | hp1 | a0001 | c0001 | t0023 | g0048 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01168 | hp2 | a0001 | c0001 | t0019 | g0166 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0175 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0085 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01192 | hp1 | a0001 | c0001 | t0032 | g0002 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01243 | hp1 | a0001 | c0001 | t0054 | g0055 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01243 | hp2 | a0001 | c0001 | t0010 | g0007 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0025 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01261 | hp1 | a0001 | c0001 | t0012 | g0025 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0062 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01358 | hp1 | a0001 | c0001 | t0012 | g0002 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01361 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0042 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0049 | EUR | IBS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01516 | hp2 | a0001 | c0001 | t0014 | g0011 | EUR | IBS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0011 | EUR | IBS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01884 | hp1 | a0001 | c0002 | t0026 | g0182 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01891 | hp1 | a0001 | c0001 | t0016 | g0030 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0092 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01928 | hp2 | a0001 | c0001 | t0012 | g0063 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01934 | hp1 | a0001 | c0001 | t0030 | g0002 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01934 | hp2 | a0001 | c0002 | t0034 | g0005 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01952 | hp2 | a0001 | c0001 | t0030 | g0044 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01975 | hp2 | a0001 | c0001 | t0021 | g0002 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01978 | hp2 | a0001 | c0009 | t0061 | g0028 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01981 | hp2 | a0001 | c0001 | t0012 | g0002 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01993 | hp1 | a0001 | c0001 | t0055 | g0043 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02015 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02027 | hp1 | a0001 | c0001 | t0015 | g0029 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02040 | hp1 | a0001 | c0001 | t0023 | g0074 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0067 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02056 | hp2 | a0001 | c0001 | t0015 | g0029 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02080 | hp2 | a0001 | c0001 | t0008 | g0073 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02083 | hp2 | a0001 | c0001 | t0007 | g0019 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02145 | hp1 | a0001 | c0001 | t0042 | g0179 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02145 | hp2 | a0001 | c0001 | t0033 | g0161 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02148 | hp2 | a0001 | c0001 | t0039 | g0010 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02257 | hp1 | a0001 | c0001 | t0032 | g0028 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02258 | hp1 | a0001 | c0001 | t0069 | g0078 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0032 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02280 | hp1 | a0001 | c0001 | t0037 | g0080 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02280 | hp2 | a0001 | c0001 | t0020 | g0008 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02293 | hp1 | a0001 | c0001 | t0065 | g0060 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0083 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02451 | hp1 | a0001 | c0001 | t0059 | g0091 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02523 | hp2 | a0001 | c0001 | t0015 | g0069 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02572 | hp2 | a0001 | c0001 | t0043 | g0094 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02615 | hp1 | a0001 | c0007 | t0027 | g0172 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0022 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0042 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02630 | hp1 | a0001 | c0001 | t0027 | g0169 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02630 | hp2 | a0001 | c0001 | t0062 | g0070 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02647 | hp2 | a0001 | c0001 | t0046 | g0013 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02698 | hp1 | a0001 | c0001 | t0066 | g0057 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02717 | hp1 | a0001 | c0001 | t0020 | g0008 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0007 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0171 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02723 | hp2 | a0001 | c0001 | t0031 | g0125 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0002 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02809 | hp2 | a0002 | c0003 | t0064 | g0088 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02886 | hp1 | a0003 | c0008 | t0001 | g0117 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02895 | hp1 | a0001 | c0001 | t0016 | g0162 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02895 | hp2 | a0001 | c0004 | t0010 | g0007 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02896 | hp1 | a0001 | c0001 | t0028 | g0007 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02897 | hp1 | a0001 | c0004 | t0028 | g0007 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02922 | hp1 | a0001 | c0001 | t0049 | g0032 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02965 | hp1 | a0001 | c0001 | t0050 | g0093 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02965 | hp2 | a0001 | c0002 | t0009 | g0005 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02970 | hp1 | a0001 | c0002 | t0036 | g0005 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0021 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02976 | hp1 | a0001 | c0001 | t0057 | g0106 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02976 | hp2 | a0001 | c0001 | t0019 | g0163 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03041 | hp1 | a0001 | c0001 | t0029 | g0008 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03041 | hp2 | a0001 | c0002 | t0024 | g0187 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0170 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03139 | hp2 | a0001 | c0002 | t0009 | g0005 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03195 | hp1 | a0001 | c0001 | t0033 | g0160 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03209 | hp1 | a0001 | c0001 | t0017 | g0017 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03209 | hp2 | a0001 | c0002 | t0009 | g0188 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03225 | hp1 | a0001 | c0001 | t0029 | g0008 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03225 | hp2 | a0001 | c0001 | t0060 | g0122 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03453 | hp1 | a0001 | c0001 | t0031 | g0090 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0007 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0097 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03491 | hp2 | a0001 | c0001 | t0013 | g0002 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03492 | hp1 | a0001 | c0001 | t0013 | g0002 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03516 | hp1 | a0001 | c0001 | t0038 | g0173 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03516 | hp2 | a0001 | c0001 | t0063 | g0159 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03540 | hp2 | a0001 | c0002 | t0025 | g0185 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0022 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03579 | hp2 | a0001 | c0002 | t0026 | g0005 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03704 | hp1 | a0001 | c0001 | t0014 | g0065 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03704 | hp2 | a0001 | c0001 | t0018 | g0010 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0018 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04115 | hp1 | a0001 | c0001 | t0040 | g0168 | SAS | STU | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | STU | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04184 | hp1 | a0001 | c0001 | t0019 | g0023 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04204 | hp1 | a0004 | c0005 | t0004 | g0053 | SAS | STU | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0045 | SAS | STU | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | YRI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18522 | hp2 | a0001 | c0001 | t0044 | g0181 | AFR | YRI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18747 | hp1 | a0001 | c0001 | t0021 | g0047 | EAS | CHB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0030 | AFR | YRI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18906 | hp2 | a0001 | c0002 | t0009 | g0005 | AFR | YRI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18947 | hp2 | a0001 | c0001 | t0006 | g0167 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18949 | hp2 | a0001 | c0001 | t0022 | g0079 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18950 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18959 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18960 | hp2 | a0001 | c0001 | t0023 | g0021 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18961 | hp1 | a0001 | c0001 | t0012 | g0026 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18963 | hp2 | a0001 | c0001 | t0008 | g0056 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18964 | hp2 | a0001 | c0001 | t0051 | g0016 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18977 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18985 | hp1 | a0001 | c0001 | t0006 | g0176 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18986 | hp2 | a0001 | c0001 | t0014 | g0076 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18995 | hp1 | a0001 | c0001 | t0014 | g0068 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18999 | hp2 | a0001 | c0001 | t0022 | g0019 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19000 | hp1 | a0001 | c0001 | t0070 | g0006 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0064 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19030 | hp1 | a0001 | c0001 | t0048 | g0180 | AFR | LWK | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19030 | hp2 | a0002 | c0003 | t0056 | g0087 | AFR | LWK | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0177 | AFR | LWK | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19043 | hp2 | a0001 | c0001 | t0067 | g0134 | AFR | LWK | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19054 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19057 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19060 | hp1 | a0001 | c0001 | t0068 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19062 | hp2 | a0001 | c0001 | t0017 | g0174 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19064 | hp1 | a0001 | c0001 | t0021 | g0054 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19077 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19077 | hp2 | a0001 | c0001 | t0058 | g0036 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19083 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19240 | hp1 | a0001 | c0002 | t0025 | g0186 | AFR | YRI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19240 | hp2 | a0001 | c0002 | t0024 | g0183 | AFR | YRI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | ASW | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20752 | hp1 | a0001 | c0001 | t0007 | g0011 | EUR | TSI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0012 | EUR | TSI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20905 | hp1 | a0001 | c0001 | t0007 | g0051 | SAS | GIH | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20905 | hp2 | a0001 | c0001 | t0047 | g0041 | SAS | GIH | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01123 | hp1 | a0001 | c0001 | t0017 | g0010 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01123 | hp2 | a0001 | c0001 | t0008 | g0018 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02109 | hp2 | a0001 | c0001 | t0015 | g0071 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02486 | hp1 | a0001 | c0001 | t0045 | g0013 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02559 | hp1 | a0001 | c0002 | t0009 | g0005 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02559 | hp2 | a0001 | c0001 | t0010 | g0178 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03471 | hp1 | a0001 | c0001 | t0020 | g0008 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0022 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG06807 | hp1 | a0001 | c0002 | t0009 | g0005 | AFR | USA | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | USA | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | USA | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0084 | AFR | USA | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA21309 | hp1 | a0001 | c0001 | t0041 | g0164 | AFR | LWK | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | LWK | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0126 | REF | REF | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0041 | REF | REF | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:15999994
|
C | T | 1 | a0003 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.146C>T | p.Pro49Leu | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 1/10 | 171/3050 | 146/1143 | 49/380 | chr17 | 15999994 | ||
| chr17:16000227
|
G | C | 1 | a0004 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.294G>C | p.Gln98His | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/10 | 319/3050 | 294/1143 | 98/380 | chr17 | 16000227 | ||
| chr17:16025098
|
C | T | 1 | a0002 | 3 | HG02809.hp2 HG03486.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.758C>T | p.Pro253Leu | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/10 | 783/3050 | 758/1143 | 253/380 | chr17 | 16025098 | ||
| chr17:16027383
|
C | T | 1 | a0005 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1004C>T | p.Thr335Ile | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1029/3050 | 1004/1143 | 335/380 | chr17 | 16027383 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:15999873
|
C | T | 1 | a0001c0009 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.25C>T | p.Leu9Leu | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 1/10 | 50/3050 | 25/1143 | 9/380 | chr17 | 15999873 | ||
| chr17:16001965
|
C | T | 1 | a0001c0004 | 2 | HG02895.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.363C>T | p.Asp121Asp | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/10 | 388/3050 | 363/1143 | 121/380 | chr17 | 16001965 | ||
| chr17:16004254
|
G | A | 2 | a0001c0002a0005c0006 | 15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
synonymous_variant | LOW | c.573G>A | p.Ala191Ala | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/10 | 598/3050 | 573/1143 | 191/380 | chr17 | 16004254 | ||
| chr17:16025021
|
A | G | 1 | a0001c0007 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.681A>G | p.Glu227Glu | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/10 | 706/3050 | 681/1143 | 227/380 | chr17 | 16025021 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:15999834
|
G | A | 7 | a0001c0002t0009a0001c0002t0024a0001c0002t0025others(4): Show | 15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-15G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 1/10 | 15 | chr17 | 15999834 | |||||
| chr17:15999848
|
C | T | 1 | a0001c0001t0070 | 1 | NA19000.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 1/10 | 1 | chr17 | 15999848 | |||||
| chr17:16027549
|
G | A | 1 | a0001c0001t0037 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 27 | chr17 | 16027549 | |||||
| chr17:16027568
|
T | C | 18 | a0001c0001t0006a0001c0001t0010a0001c0001t0016others(15): Show | 41 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*46T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 46 | chr17 | 16027568 | |||||
| chr17:16027594
|
C | G | 1 | a0001c0001t0069 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*72C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 72 | chr17 | 16027594 | |||||
| chr17:16027605
|
G | A | 2 | a0001c0001t0045a0001c0001t0046 | 2 | HG02486.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*83G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 83 | chr17 | 16027605 | |||||
| chr17:16027633
|
G | A | 1 | a0001c0001t0047 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*111G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 111 | chr17 | 16027633 | |||||
| chr17:16027717
|
A | G | 1 | a0001c0001t0033 | 2 | HG02145.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*195A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 195 | chr17 | 16027717 | |||||
| chr17:16027735
|
G | T | 1 | a0001c0001t0044 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*213G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 213 | chr17 | 16027735 | |||||
| chr17:16027748
|
T | C | 6 | a0001c0001t0011a0001c0001t0020a0001c0001t0029others(3): Show | 13 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*226T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 226 | chr17 | 16027748 | |||||
| chr17:16027823
|
G | A | 1 | a0001c0001t0051 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*301G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 301 | chr17 | 16027823 | |||||
| chr17:16027872
|
A | G | 1 | a0001c0001t0068 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*350A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 350 | chr17 | 16027872 | |||||
| chr17:16028100
|
C | T | 1 | a0001c0001t0067 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*578C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 578 | chr17 | 16028100 | |||||
| chr17:16028122
|
G | A | 11 | a0001c0001t0006a0001c0001t0016a0001c0001t0017others(8): Show | 30 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*600G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 600 | chr17 | 16028122 | |||||
| chr17:16028231
|
T | A | 11 | a0001c0001t0006a0001c0001t0016a0001c0001t0017others(8): Show | 30 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*709T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 709 | chr17 | 16028231 | |||||
| chr17:16028379
|
G | A | 6 | a0001c0001t0013a0001c0001t0030a0001c0001t0052others(3): Show | 10 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*857G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 857 | chr17 | 16028379 | |||||
| chr17:16028493
|
G | A | 11 | a0001c0001t0006a0001c0001t0016a0001c0001t0017others(8): Show | 30 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*971G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 971 | chr17 | 16028493 | |||||
| chr17:16028534
|
T | C | 6 | a0001c0001t0011a0001c0001t0020a0001c0001t0029others(3): Show | 13 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1012T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1012 | chr17 | 16028534 | |||||
| chr17:16028674
|
C | T | 2 | a0001c0001t0020a0001c0001t0029 | 5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1152C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1152 | chr17 | 16028674 | |||||
| chr17:16028716
|
T | A | 1 | a0002c0003t0056 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1194T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1194 | chr17 | 16028716 | |||||
| chr17:16028757
|
C | CTT | 59 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(56): Show | 170 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1236_*1237dupTT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1238 | INFO_REALIGN_3_PRIME | chr17 | 16028757 | ||||
| chr17:16028818
|
C | CA | 7 | a0001c0001t0002a0001c0001t0011a0001c0001t0019others(4): Show | 40 | HG00673.hp2 HG01168.hp2 HG01261.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1324dupA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
C | CAA | 3 | a0001c0001t0006a0001c0001t0018a0001c0001t0058 | 16 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1323_*1324dupAA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
C | CAAA | 5 | a0001c0001t0016a0001c0001t0017a0001c0001t0039others(2): Show | 9 | HG01123.hp1 HG01891.hp1 HG02148.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1322_*1324dupAAA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
C | CAAAAAAA | 3 | a0001c0001t0014a0001c0001t0038a0001c0002t0025 | 7 | HG01516.hp2 HG03516.hp1 HG03540.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1318_*1324dupAAAA others(3): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
C | CAAAAAAA others(1): Show |
5 | a0001c0001t0004a0001c0001t0022a0001c0001t0037others(2): Show | 29 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1317_*1324dupAAAA others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
C | CAAAAAAA others(2): Show |
5 | a0001c0001t0007a0001c0001t0032a0001c0001t0062others(2): Show | 20 | HG01099.hp2 HG01192.hp1 HG01361.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1316_*1324dupAAAA others(5): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0005a0001c0001t0013 | 19 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1315_*1324dupAAAA others(6): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
C | CAAAAAAA others(4): Show |
4 | a0001c0001t0008a0001c0001t0030a0001c0001t0054others(1): Show | 12 | HG01123.hp2 HG01243.hp1 HG01934.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1314_*1324dupAAAA others(7): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0052a0001c0001t0053a0001c0009t0061others(1): Show | 4 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1313_*1324dupAAAA others(8): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0021 | 3 | HG01975.hp2 NA18747.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1312_*1324dupAAAA others(9): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0012 | 5 | HG01261.hp1 HG01358.hp1 HG01928.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1311_*1324dupAAAA others(10): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
C | CAAAAAAA others(8): Show |
1 | a0001c0002t0034 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1310_*1324dupAAAA others(11): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
CA | C | 5 | a0001c0001t0003a0001c0001t0046a0001c0001t0050others(2): Show | 29 | HG01070.hp2 HG01192.hp2 HG01433.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1324delA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1324 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
CAAAAAAA | C | 2 | a0001c0001t0010a0001c0004t0010 | 6 | HG01243.hp2 HG02559.hp2 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1318_*1324delAAAA others(3): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1318 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
CAAAAAAA others(1): Show |
C | 3 | a0001c0001t0015a0001c0001t0028a0001c0004t0028 | 6 | HG02027.hp1 HG02056.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1317_*1324delAAAA others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1317 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1315_*1324delAAAA others(6): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1315 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0066 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314_*1324delAAAA others(7): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1314 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028818
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0060 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1312_*1324delAAAA others(9): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1312 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | ||||
| chr17:16028855
|
A | G | 1 | a0001c0001t0022 | 3 | HG00408.hp1 NA18949.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1333A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1333 | chr17 | 16028855 | |||||
| chr17:16028880
|
G | C | 3 | a0001c0001t0016a0001c0001t0027a0001c0007t0027 | 5 | HG01891.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1358G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1358 | chr17 | 16028880 | |||||
| chr17:16028991
|
G | A | 1 | a0001c0001t0048 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1469G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1469 | chr17 | 16028991 | |||||
| chr17:16029065
|
A | G | 3 | a0001c0001t0018a0001c0001t0039a0001c0001t0040 | 5 | HG00323.hp2 HG01106.hp1 HG02148.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1543A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1543 | chr17 | 16029065 | |||||
| chr17:16029106
|
T | TGAG | 3 | a0001c0001t0030a0001c0001t0052a0001c0001t0055 | 4 | HG00639.hp2 HG01934.hp1 HG01952.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1584_*1585insGAG | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1585 | chr17 | 16029106 | |||||
| chr17:16029108
|
G | GAGTAAAA others(1): Show |
3 | a0001c0001t0030a0001c0001t0052a0001c0001t0055 | 4 | HG00639.hp2 HG01934.hp1 HG01952.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1586_*1587insAGTA others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1587 | chr17 | 16029108 | |||||
| chr17:16029111
|
T | C | 1 | a0001c0001t0032 | 2 | HG01192.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1589T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1589 | chr17 | 16029111 | |||||
| chr17:16029188
|
T | G | 1 | a0001c0001t0062 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1666T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1666 | chr17 | 16029188 | |||||
| chr17:16029260
|
T | C | 3 | a0001c0001t0011a0001c0001t0049a0001c0001t0050 | 7 | HG01891.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1738T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1738 | chr17 | 16029260 | |||||
| chr17:16029313
|
T | C | 34 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(31): Show | 115 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*1791T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1791 | chr17 | 16029313 | |||||
| chr17:16029342
|
C | CTGAT | 2 | a0001c0001t0031a0001c0001t0059 | 3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1823_*1826dupATTG | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1827 | INFO_REALIGN_3_PRIME | chr17 | 16029342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:16000288
|
C | A | 80 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(77): Show | 96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.312+43C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16000288 | ||||||
| chr17:16000555
|
C | A | 3 | a0001c0001t0016g0030a0002c0003t0056g0087a0002c0003t0064g0088 | 4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+310C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16000555 | ||||||
| chr17:16000612
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.312+367G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16000612 | ||||||
| chr17:16000714
|
G | A | 1 | a0001c0001t0001g0031 | 2 | NA18973.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.312+469G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16000714 | ||||||
| chr17:16000891
|
A | G | 1 | a0002c0003t0064g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312+646A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16000891 | ||||||
| chr17:16001012
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.312+767A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001012 | ||||||
| chr17:16001136
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.313-779C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001136 | ||||||
| chr17:16001179
|
C | G | 1 | a0001c0001t0004g0085 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.313-736C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001179 | ||||||
| chr17:16001187
|
C | T | 11 | a0001c0002t0009g0005a0001c0002t0009g0188a0001c0002t0024g0183others(8): Show | 15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.313-728C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001187 | ||||||
| chr17:16001288
|
C | T | 2 | a0001c0001t0004g0083a0001c0001t0007g0084 | 2 | HG02293.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.313-627C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001288 | ||||||
| chr17:16001337
|
A | G | 11 | a0001c0002t0009g0005a0001c0002t0009g0188a0001c0002t0024g0183others(8): Show | 15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.313-578A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001337 | ||||||
| chr17:16001734
|
G | A | 2 | a0001c0001t0031g0090a0001c0001t0059g0091 | 2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.313-181G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001734 | ||||||
| chr17:16001764
|
T | C | 10 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(7): Show | 15 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.313-151T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001764 | ||||||
| chr17:16001788
|
G | C | 11 | a0001c0002t0009g0005a0001c0002t0009g0188a0001c0002t0024g0183others(8): Show | 15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.313-127G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001788 | ||||||
| chr17:16001876
|
A | G | 89 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(86): Show | 107 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.313-39A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001876 | ||||||
| chr17:16002119
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.423+94G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002119 | ||||||
| chr17:16002121
|
T | C | 2 | a0001c0001t0031g0090a0001c0001t0059g0091 | 2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.423+96T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002121 | ||||||
| chr17:16002282
|
G | A | 26 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(23): Show | 33 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.423+257G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002282 | ||||||
| chr17:16002396
|
C | T | 11 | a0001c0002t0009g0005a0001c0002t0009g0188a0001c0002t0024g0183others(8): Show | 15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.423+371C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002396 | ||||||
| chr17:16002638
|
C | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(44): Show | 63 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(60): Show |
intron_variant | MODIFIER | c.424-155C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002638 | ||||||
| chr17:16002643
|
G | T | 1 | a0001c0001t0016g0030 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.424-150G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002643 | ||||||
| chr17:16002646
|
T | G | 6 | a0001c0001t0001g0035a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG02056.hp1 NA18961.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-147T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002646 | ||||||
| chr17:16002721
|
G | A | 1 | a0001c0001t0004g0024 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.424-72G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002721 | ||||||
| chr17:16003077
|
C | T | 162 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(159): Show | 202 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.462+246C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003077 | ||||||
| chr17:16003078
|
T | C | 80 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(77): Show | 96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.462+247T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003078 | ||||||
| chr17:16003114
|
G | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(32): Show | 46 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.462+283G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003114 | ||||||
| chr17:16003239
|
A | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(44): Show | 60 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(57): Show |
intron_variant | MODIFIER | c.462+408A>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003239 | ||||||
| chr17:16003250
|
T | C | 7 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(4): Show | 12 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.462+419T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003250 | ||||||
| chr17:16003332
|
C | T | 80 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(77): Show | 96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.463-499C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003332 | ||||||
| chr17:16003404
|
C | T | 1 | a0001c0001t0006g0176 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.463-427C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003404 | ||||||
| chr17:16003405
|
A | G | 31 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(28): Show | 42 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.463-426A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003405 | ||||||
| chr17:16003422
|
C | CTTAT | 4 | a0001c0001t0020g0008a0001c0001t0029g0008a0001c0001t0031g0090others(1): Show | 7 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.463-379_463-376dup others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 16003422 | |||||
| chr17:16003422
|
C | CTTATTTA others(5): Show |
1 | a0001c0001t0059g0091 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.463-387_463-376dup others(12): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 16003422 | |||||
| chr17:16003422
|
CTTAT | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(213): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.463-379_463-376del others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 16003422 | |||||
| chr17:16003422
|
CTTATTTA others(1): Show |
C | 7 | a0001c0001t0010g0007a0001c0001t0010g0177a0001c0001t0010g0178others(4): Show | 9 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.463-383_463-376del others(8): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 16003422 | |||||
| chr17:16003466
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.463-365G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003466 | ||||||
| chr17:16003518
|
T | C | 5 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(2): Show | 7 | HG01891.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.463-313T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003518 | ||||||
| chr17:16003572
|
T | C | 56 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(53): Show | 74 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(71): Show |
intron_variant | MODIFIER | c.463-259T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003572 | ||||||
| chr17:16003598
|
G | A | 80 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(77): Show | 96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.463-233G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003598 | ||||||
| chr17:16003706
|
G | A | 2 | a0001c0001t0030g0044a0001c0001t0055g0043 | 2 | HG01952.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.463-125G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003706 | ||||||
| chr17:16003719
|
T | A | 1 | a0001c0001t0004g0045 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.463-112T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003719 | ||||||
| chr17:16003743
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.463-88A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003743 | ||||||
| chr17:16003770
|
C | CAT | 15 | a0001c0001t0001g0004a0001c0001t0001g0112a0001c0001t0001g0142others(12): Show | 20 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.463-47_463-46dupTA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 16003770 | |||||
| chr17:16003805
|
G | T | 1 | a0001c0001t0004g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.463-26G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003805 | ||||||
| chr17:16003994
|
G | A | 1 | a0001c0001t0005g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.519+107G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 5/9 | chr17 | 16003994 | ||||||
| chr17:16004016
|
T | C | 1 | a0001c0001t0043g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.519+129T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 5/9 | chr17 | 16004016 | ||||||
| chr17:16004153
|
G | GA | 57 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(54): Show | 72 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(69): Show |
intron_variant | MODIFIER | c.520-42dupA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr17 | 16004153 | |||||
| chr17:16004450
|
G | A | 26 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(23): Show | 32 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.581+188G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16004450 | ||||||
| chr17:16004581
|
G | A | 1 | a0002c0003t0056g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.581+319G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16004581 | ||||||
| chr17:16004870
|
G | T | 2 | a0001c0001t0033g0160a0001c0001t0033g0161 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.581+608G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16004870 | ||||||
| chr17:16004940
|
C | G | 7 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(4): Show | 12 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.581+678C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16004940 | ||||||
| chr17:16004997
|
C | A | 2 | a0001c0001t0031g0090a0001c0001t0059g0091 | 2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.581+735C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16004997 | ||||||
| chr17:16005049
|
G | A | 1 | a0001c0001t0010g0177 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.581+787G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005049 | ||||||
| chr17:16005116
|
T | C | 1 | a0001c0002t0026g0182 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.581+854T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005116 | ||||||
| chr17:16005143
|
CAATT | C | 3 | a0001c0001t0031g0090a0001c0001t0043g0094a0001c0001t0059g0091 | 3 | HG02451.hp1 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.581+883_581+886del others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 16005143 | |||||
| chr17:16005254
|
G | A | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.581+992G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005254 | ||||||
| chr17:16005397
|
C | T | 3 | a0001c0001t0033g0160a0001c0001t0033g0161a0001c0001t0063g0159 | 3 | HG02145.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.582-1077C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005397 | ||||||
| chr17:16005458
|
G | A | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.582-1016G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005458 | ||||||
| chr17:16005508
|
A | AC | 79 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(76): Show | 103 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(100): Show |
intron_variant | MODIFIER | c.582-966_582-965ins others(1): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005508 | ||||||
| chr17:16005533
|
T | C | 1 | a0001c0001t0004g0045 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.582-941T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005533 | ||||||
| chr17:16005559
|
C | T | 1 | a0001c0001t0016g0030 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.582-915C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005559 | ||||||
| chr17:16005597
|
C | G | 1 | a0001c0002t0009g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.582-877C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005597 | ||||||
| chr17:16005842
|
G | A | 23 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(20): Show | 29 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.582-632G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005842 | ||||||
| chr17:16005892
|
G | T | 8 | a0001c0001t0010g0007a0001c0001t0010g0177a0001c0001t0010g0178others(5): Show | 10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.582-582G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005892 | ||||||
| chr17:16005945
|
G | A | 6 | a0001c0001t0010g0007a0001c0001t0010g0178a0001c0001t0028g0007others(3): Show | 8 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.582-529G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005945 | ||||||
| chr17:16005991
|
G | A | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.582-483G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005991 | ||||||
| chr17:16006135
|
C | T | 2 | a0001c0001t0002g0141a0001c0001t0003g0040 | 3 | NA18947.hp1 NA18962.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.582-339C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16006135 | ||||||
| chr17:16006414
|
A | G | 147 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(144): Show | 183 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.582-60A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16006414 | ||||||
| chr17:16006664
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.676+96A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006664 | ||||||
| chr17:16006670
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.676+102A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006670 | ||||||
| chr17:16006674
|
A | G | 34 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(31): Show | 42 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.676+106A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006674 | ||||||
| chr17:16006735
|
A | C | 5 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(2): Show | 7 | HG01891.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.676+167A>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006735 | ||||||
| chr17:16006764
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.676+196G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006764 | ||||||
| chr17:16006819
|
T | C | 3 | a0001c0001t0033g0160a0001c0001t0033g0161a0001c0001t0063g0159 | 3 | HG02145.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.676+251T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006819 | ||||||
| chr17:16006827
|
T | C | 11 | a0001c0002t0009g0005a0001c0002t0009g0188a0001c0002t0024g0183others(8): Show | 15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.676+259T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006827 | ||||||
| chr17:16006972
|
A | G | 80 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(77): Show | 96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.676+404A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006972 | ||||||
| chr17:16007084
|
G | A | 2 | a0001c0001t0031g0090a0001c0001t0059g0091 | 2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.676+516G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007084 | ||||||
| chr17:16007111
|
T | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.676+543T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007111 | ||||||
| chr17:16007127
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.676+559G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007127 | ||||||
| chr17:16007376
|
CT | C | 26 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(23): Show | 32 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.676+809delT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007376 | ||||||
| chr17:16007439
|
AGTTTTTT | A | 51 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(48): Show | 66 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.676+891_676+897del others(7): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16007439 | |||||
| chr17:16007439
|
AGTTTTTT others(7): Show |
A | 1 | a0001c0001t0004g0085 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.676+884_676+897del others(14): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16007439 | |||||
| chr17:16007470
|
C | T | 66 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(63): Show | 86 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.676+902C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007470 | ||||||
| chr17:16007666
|
C | T | 1 | a0001c0001t0003g0139 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.676+1098C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007666 | ||||||
| chr17:16007752
|
C | T | 3 | a0001c0001t0031g0090a0001c0001t0043g0094a0001c0001t0059g0091 | 3 | HG02451.hp1 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.676+1184C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007752 | ||||||
| chr17:16007791
|
T | G | 159 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(156): Show | 199 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.676+1223T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007791 | ||||||
| chr17:16007889
|
A | G | 1 | a0001c0001t0048g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.676+1321A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007889 | ||||||
| chr17:16007945
|
A | G | 1 | a0001c0001t0043g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.676+1377A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007945 | ||||||
| chr17:16008118
|
C | T | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+1550C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008118 | ||||||
| chr17:16008211
|
C | G | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+1643C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008211 | ||||||
| chr17:16008377
|
T | G | 8 | a0001c0001t0010g0007a0001c0001t0010g0177a0001c0001t0010g0178others(5): Show | 10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.676+1809T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008377 | ||||||
| chr17:16008600
|
C | T | 1 | a0001c0001t0016g0030 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.676+2032C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008600 | ||||||
| chr17:16008619
|
C | T | 23 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(20): Show | 29 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.676+2051C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008619 | ||||||
| chr17:16008658
|
G | A | 1 | a0001c0001t0010g0177 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676+2090G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008658 | ||||||
| chr17:16008666
|
C | T | 1 | a0001c0001t0057g0106 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.676+2098C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008666 | ||||||
| chr17:16008781
|
C | T | 1 | a0001c0001t0031g0090 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.676+2213C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008781 | ||||||
| chr17:16008796
|
T | C | 1 | a0001c0001t0016g0162 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.676+2228T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008796 | ||||||
| chr17:16008825
|
G | C | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+2257G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008825 | ||||||
| chr17:16009014
|
ATCCATTA others(25): Show |
A | 2 | a0001c0001t0033g0160a0001c0001t0033g0161 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.676+2448_676+2479d others(34): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16009014 | |||||
| chr17:16009021
|
A | G | 1 | a0001c0001t0004g0081 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.676+2453A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009021 | ||||||
| chr17:16009041
|
G | A | 8 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(5): Show | 13 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.676+2473G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009041 | ||||||
| chr17:16009115
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0058g0036 | 2 | NA18950.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.676+2547G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009115 | ||||||
| chr17:16009139
|
G | C | 1 | a0001c0002t0026g0182 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.676+2571G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009139 | ||||||
| chr17:16009198
|
CAAGT | C | 2 | a0001c0001t0001g0016a0001c0001t0051g0016 | 4 | HG02074.hp1 NA18964.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+2635_676+2638d others(6): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16009198 | |||||
| chr17:16009270
|
A | AGT | 3 | a0001c0001t0016g0030a0002c0003t0056g0087a0002c0003t0064g0088 | 4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+2705_676+2706d others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16009270 | |||||
| chr17:16009400
|
G | A | 3 | a0001c0001t0016g0030a0002c0003t0056g0087a0002c0003t0064g0088 | 4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+2832G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009400 | ||||||
| chr17:16009442
|
C | A | 1 | a0001c0001t0019g0163 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.676+2874C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009442 | ||||||
| chr17:16009500
|
C | CT | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+2941dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16009500 | |||||
| chr17:16009565
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00621.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.676+2997T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009565 | ||||||
| chr17:16009801
|
A | G | 2 | a0001c0001t0031g0090a0001c0001t0059g0091 | 2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.676+3233A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009801 | ||||||
| chr17:16010126
|
T | C | 147 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(144): Show | 183 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.676+3558T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010126 | ||||||
| chr17:16010129
|
C | T | 3 | a0001c0001t0016g0030a0002c0003t0056g0087a0002c0003t0064g0088 | 4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+3561C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010129 | ||||||
| chr17:16010167
|
A | AT | 20 | a0001c0001t0001g0089a0001c0001t0001g0111a0001c0001t0001g0136others(17): Show | 21 | HG00642.hp1 HG00673.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.676+3623dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16010167 | |||||
| chr17:16010167
|
AT | A | 19 | a0001c0001t0001g0014a0001c0001t0001g0109a0001c0001t0001g0114others(16): Show | 26 | HG01109.hp2 HG01168.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.676+3623delT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16010167 | |||||
| chr17:16010167
|
ATTTTT | A | 61 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(58): Show | 81 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(78): Show |
intron_variant | MODIFIER | c.676+3619_676+3623d others(7): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16010167 | |||||
| chr17:16010206
|
C | G | 1 | a0001c0007t0027g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.676+3638C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010206 | ||||||
| chr17:16010234
|
T | A | 23 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(20): Show | 29 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.676+3666T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010234 | ||||||
| chr17:16010242
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.676+3674C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010242 | ||||||
| chr17:16010306
|
C | T | 1 | a0001c0001t0016g0030 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.676+3738C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010306 | ||||||
| chr17:16010432
|
A | G | 34 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(31): Show | 42 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.676+3864A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010432 | ||||||
| chr17:16010462
|
G | A | 8 | a0001c0001t0010g0007a0001c0001t0010g0177a0001c0001t0010g0178others(5): Show | 10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.676+3894G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010462 | ||||||
| chr17:16010505
|
C | T | 23 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(20): Show | 29 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.676+3937C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010505 | ||||||
| chr17:16010589
|
C | G | 2 | a0001c0001t0005g0077a0001c0001t0069g0078 | 2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.676+4021C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010589 | ||||||
| chr17:16010626
|
C | T | 5 | a0001c0001t0004g0012a0001c0001t0004g0049a0001c0001t0004g0082others(2): Show | 7 | HG00735.hp2 HG01099.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.676+4058C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010626 | ||||||
| chr17:16010640
|
A | G | 2 | a0001c0002t0025g0185a0001c0002t0025g0186 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.676+4072A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010640 | ||||||
| chr17:16010704
|
C | G | 1 | a0001c0001t0052g0061 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.676+4136C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010704 | ||||||
| chr17:16010785
|
C | T | 6 | a0001c0001t0006g0017a0001c0001t0006g0042a0001c0001t0006g0170others(3): Show | 9 | HG00741.hp1 HG01433.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.676+4217C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010785 | ||||||
| chr17:16011153
|
A | G | 2 | a0001c0001t0002g0135a0001c0001t0002g0138 | 2 | HG02738.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.676+4585A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011153 | ||||||
| chr17:16011215
|
C | G | 1 | a0002c0003t0056g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.676+4647C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011215 | ||||||
| chr17:16011462
|
C | T | 23 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(20): Show | 29 | HG01192.hp2 HG02109.hp1 HG02486.hp1 others(26): Show |
intron_variant | MODIFIER | c.676+4894C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011462 | ||||||
| chr17:16011465
|
G | A | 3 | a0001c0001t0031g0090a0001c0001t0043g0094a0001c0001t0059g0091 | 3 | HG02451.hp1 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.676+4897G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011465 | ||||||
| chr17:16011498
|
G | C | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+4930G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011498 | ||||||
| chr17:16011672
|
A | G | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+5104A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011672 | ||||||
| chr17:16011758
|
A | G | 146 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(143): Show | 182 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.676+5190A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011758 | ||||||
| chr17:16012021
|
CT | C | 23 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(20): Show | 29 | HG01192.hp2 HG02109.hp1 HG02486.hp1 others(26): Show |
intron_variant | MODIFIER | c.676+5464delT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16012021 | |||||
| chr17:16012144
|
G | T | 3 | a0001c0001t0016g0162a0001c0001t0027g0169a0001c0007t0027g0172 | 3 | HG02615.hp1 HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.676+5576G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012144 | ||||||
| chr17:16012260
|
G | A | 2 | a0001c0001t0020g0008a0001c0001t0029g0008 | 5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+5692G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012260 | ||||||
| chr17:16012595
|
A | G | 1 | a0001c0001t0016g0030 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.676+6027A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012595 | ||||||
| chr17:16012600
|
A | G | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+6032A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012600 | ||||||
| chr17:16012708
|
T | C | 2 | a0001c0001t0020g0008a0001c0001t0029g0008 | 5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+6140T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012708 | ||||||
| chr17:16012758
|
G | A | 2 | a0001c0001t0020g0008a0001c0001t0029g0008 | 5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+6190G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012758 | ||||||
| chr17:16012829
|
C | T | 1 | a0001c0001t0043g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.676+6261C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012829 | ||||||
| chr17:16013094
|
C | T | 1 | a0001c0001t0067g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.676+6526C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013094 | ||||||
| chr17:16013178
|
C | T | 3 | a0001c0001t0031g0090a0001c0001t0043g0094a0001c0001t0059g0091 | 3 | HG02451.hp1 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.676+6610C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013178 | ||||||
| chr17:16013312
|
C | T | 7 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(4): Show | 12 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.676+6744C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013312 | ||||||
| chr17:16013326
|
A | T | 6 | a0001c0001t0006g0017a0001c0001t0006g0042a0001c0001t0006g0170others(3): Show | 9 | HG00741.hp1 HG01433.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.676+6758A>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013326 | ||||||
| chr17:16013422
|
T | C | 1 | a0001c0001t0004g0045 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.676+6854T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013422 | ||||||
| chr17:16013440
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.676+6872T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013440 | ||||||
| chr17:16013532
|
A | G | 1 | a0001c0001t0016g0162 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.676+6964A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013532 | ||||||
| chr17:16013683
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.676+7115A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013683 | ||||||
| chr17:16013955
|
G | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG00738.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.676+7387G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013955 | ||||||
| chr17:16014114
|
T | C | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.676+7546T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014114 | ||||||
| chr17:16014212
|
C | T | 1 | a0001c0001t0016g0030 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.676+7644C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014212 | ||||||
| chr17:16014225
|
T | C | 2 | a0001c0001t0001g0095a0003c0008t0001g0117 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.676+7657T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014225 | ||||||
| chr17:16014404
|
C | G | 32 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(29): Show | 41 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.676+7836C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014404 | ||||||
| chr17:16014568
|
T | C | 7 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(4): Show | 12 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.676+8000T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014568 | ||||||
| chr17:16014591
|
G | A | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+8023G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014591 | ||||||
| chr17:16014682
|
G | A | 11 | a0001c0002t0009g0005a0001c0002t0009g0188a0001c0002t0024g0183others(8): Show | 15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.676+8114G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014682 | ||||||
| chr17:16014814
|
C | G | 1 | a0001c0001t0048g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.676+8246C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014814 | ||||||
| chr17:16014884
|
G | T | 1 | a0002c0003t0064g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.676+8316G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014884 | ||||||
| chr17:16014908
|
G | A | 160 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(157): Show | 200 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.676+8340G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014908 | ||||||
| chr17:16015087
|
T | C | 3 | a0001c0001t0016g0030a0002c0003t0056g0087a0002c0003t0064g0088 | 4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+8519T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015087 | ||||||
| chr17:16015100
|
G | T | 1 | a0001c0001t0002g0131 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.676+8532G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015100 | ||||||
| chr17:16015103
|
T | C | 8 | a0001c0001t0010g0007a0001c0001t0010g0177a0001c0001t0010g0178others(5): Show | 10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.676+8535T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015103 | ||||||
| chr17:16015196
|
A | T | 1 | a0001c0001t0057g0106 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.676+8628A>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015196 | ||||||
| chr17:16015249
|
C | T | 1 | a0001c0001t0042g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.676+8681C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015249 | ||||||
| chr17:16015349
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0002g0189 | 2 | HG00673.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.676+8781A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015349 | ||||||
| chr17:16015387
|
C | CT | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+8820dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16015387 | |||||
| chr17:16015448
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0137 | 2 | NA18967.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.676+8880C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015448 | ||||||
| chr17:16015481
|
T | A | 3 | a0001c0001t0016g0030a0002c0003t0056g0087a0002c0003t0064g0088 | 4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+8913T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015481 | ||||||
| chr17:16015797
|
G | C | 1 | a0001c0001t0007g0051 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.677-9220G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015797 | ||||||
| chr17:16016030
|
T | C | 2 | a0001c0001t0038g0173a0001c0001t0041g0164 | 2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.677-8987T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016030 | ||||||
| chr17:16016098
|
C | T | 11 | a0001c0002t0009g0005a0001c0002t0009g0188a0001c0002t0024g0183others(8): Show | 15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.677-8919C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016098 | ||||||
| chr17:16016120
|
T | C | 1 | a0002c0003t0064g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.677-8897T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016120 | ||||||
| chr17:16016234
|
G | T | 6 | a0001c0001t0010g0007a0001c0001t0010g0178a0001c0001t0028g0007others(3): Show | 8 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.677-8783G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016234 | ||||||
| chr17:16016295
|
C | G | 34 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(31): Show | 42 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.677-8722C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016295 | ||||||
| chr17:16016295
|
C | T | 1 | a0001c0001t0004g0083 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.677-8722C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016295 | ||||||
| chr17:16016552
|
A | AT | 60 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0089others(57): Show | 74 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.677-8442dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16016552 | |||||
| chr17:16016552
|
A | ATT | 16 | a0001c0001t0001g0034a0001c0001t0003g0034a0001c0001t0003g0102others(13): Show | 18 | HG01192.hp2 HG01243.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.677-8443_677-8442d others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16016552 | |||||
| chr17:16016575
|
T | G | 10 | a0001c0001t0001g0118a0001c0001t0048g0180a0001c0002t0009g0005others(7): Show | 14 | HG00323.hp1 HG01109.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.677-8442T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016575 | ||||||
| chr17:16016575
|
T | TG | 10 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(7): Show | 15 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.677-8439dupG | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16016575 | |||||
| chr17:16016596
|
C | T | 3 | a0001c0001t0016g0030a0002c0003t0056g0087a0002c0003t0064g0088 | 4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.677-8421C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016596 | ||||||
| chr17:16016646
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(7): Show | 14 | HG03491.hp1 HG03654.hp2 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.677-8371C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016646 | ||||||
| chr17:16016707
|
A | G | 68 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(65): Show | 88 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(85): Show |
intron_variant | MODIFIER | c.677-8310A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016707 | ||||||
| chr17:16016789
|
C | T | 1 | a0001c0001t0022g0072 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.677-8228C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016789 | ||||||
| chr17:16016801
|
G | A | 1 | a0001c0001t0012g0063 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.677-8216G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016801 | ||||||
| chr17:16016865
|
G | T | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.677-8152G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016865 | ||||||
| chr17:16016882
|
C | T | 4 | a0001c0001t0031g0090a0001c0001t0043g0094a0001c0001t0059g0091others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.677-8135C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016882 | ||||||
| chr17:16017152
|
T | G | 2 | a0001c0001t0020g0008a0001c0001t0029g0008 | 5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-7865T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017152 | ||||||
| chr17:16017172
|
A | C | 1 | a0001c0001t0006g0167 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.677-7845A>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017172 | ||||||
| chr17:16017341
|
C | T | 1 | a0001c0001t0048g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.677-7676C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017341 | ||||||
| chr17:16017448
|
C | CA | 26 | a0001c0001t0001g0015a0001c0001t0001g0037a0001c0001t0001g0111others(23): Show | 27 | HG00621.hp1 HG00735.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.677-7547dupA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16017448 | |||||
| chr17:16017448
|
CA | C | 16 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(13): Show | 18 | HG01243.hp2 HG02080.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.677-7547delA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16017448 | |||||
| chr17:16017448
|
CAA | C | 33 | a0001c0001t0003g0100a0001c0001t0003g0102a0001c0001t0006g0017others(30): Show | 44 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.677-7548_677-7547d others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16017448 | |||||
| chr17:16017448
|
CAAA | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(17): Show | 27 | HG01192.hp2 HG01891.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.677-7549_677-7547d others(5): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16017448 | |||||
| chr17:16017448
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0128 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.677-7558_677-7547d others(14): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16017448 | |||||
| chr17:16017638
|
G | A | 9 | a0001c0001t0005g0003a0001c0001t0005g0026a0001c0001t0005g0052others(6): Show | 14 | NA18950.hp2 NA18956.hp2 NA18959.hp1 others(11): Show |
intron_variant | MODIFIER | c.677-7379G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017638 | ||||||
| chr17:16017688
|
G | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(18): Show | 27 | HG01192.hp2 HG02109.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.677-7329G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017688 | ||||||
| chr17:16017688
|
G | T | 1 | a0001c0001t0048g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.677-7329G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017688 | ||||||
| chr17:16017757
|
A | G | 142 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(139): Show | 177 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.677-7260A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017757 | ||||||
| chr17:16017854
|
G | GT | 80 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(77): Show | 96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-7159dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16017854 | |||||
| chr17:16018050
|
C | T | 7 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(4): Show | 12 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.677-6967C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018050 | ||||||
| chr17:16018105
|
G | A | 80 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(77): Show | 96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-6912G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018105 | ||||||
| chr17:16018255
|
T | TG | 80 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(77): Show | 96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-6760dupG | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16018255 | |||||
| chr17:16018304
|
A | G | 1 | a0001c0001t0015g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.677-6713A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018304 | ||||||
| chr17:16018335
|
C | G | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.677-6682C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018335 | ||||||
| chr17:16018383
|
C | T | 1 | a0001c0001t0006g0171 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.677-6634C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018383 | ||||||
| chr17:16018413
|
C | A | 1 | a0001c0001t0027g0169 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.677-6604C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018413 | ||||||
| chr17:16018519
|
T | C | 21 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(18): Show | 27 | HG01192.hp2 HG02109.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.677-6498T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018519 | ||||||
| chr17:16018678
|
C | T | 67 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(64): Show | 87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.677-6339C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018678 | ||||||
| chr17:16018819
|
T | C | 1 | a0002c0003t0001g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.677-6198T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018819 | ||||||
| chr17:16018891
|
C | G | 2 | a0001c0001t0006g0175a0001c0001t0019g0166 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.677-6126C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018891 | ||||||
| chr17:16018996
|
AGTTTGGT others(3): Show |
A | 1 | a0001c0001t0043g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.677-6015_677-6006d others(12): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16018996 | |||||
| chr17:16019072
|
C | T | 1 | a0001c0001t0015g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.677-5945C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019072 | ||||||
| chr17:16019153
|
C | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(18): Show | 27 | HG01192.hp2 HG02109.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.677-5864C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019153 | ||||||
| chr17:16019202
|
G | A | 7 | a0001c0001t0004g0019a0001c0001t0007g0019a0001c0001t0015g0029others(4): Show | 8 | HG00408.hp1 HG02015.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.677-5815G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019202 | ||||||
| chr17:16019330
|
T | A | 2 | a0001c0001t0020g0008a0001c0001t0029g0008 | 5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-5687T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019330 | ||||||
| chr17:16019533
|
G | A | 7 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(4): Show | 12 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.677-5484G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019533 | ||||||
| chr17:16019552
|
C | G | 1 | a0001c0001t0014g0068 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.677-5465C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019552 | ||||||
| chr17:16019593
|
CTG | C | 160 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(157): Show | 200 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.677-5422_677-5421d others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16019593 | |||||
| chr17:16019658
|
A | G | 1 | a0001c0001t0044g0181 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.677-5359A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019658 | ||||||
| chr17:16019791
|
G | A | 1 | a0001c0001t0043g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.677-5226G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019791 | ||||||
| chr17:16019965
|
T | TA | 53 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(50): Show | 66 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.677-5034dupA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16019965 | |||||
| chr17:16019965
|
T | TAA | 7 | a0001c0001t0010g0007a0001c0001t0010g0177a0001c0001t0010g0178others(4): Show | 9 | HG01243.hp2 HG02559.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-5035_677-5034d others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16019965 | |||||
| chr17:16020012
|
C | T | 60 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(57): Show | 75 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(72): Show |
intron_variant | MODIFIER | c.677-5005C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020012 | ||||||
| chr17:16020103
|
T | G | 1 | a0001c0001t0016g0162 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.677-4914T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020103 | ||||||
| chr17:16020360
|
TTGTC | T | 11 | a0001c0002t0009g0005a0001c0002t0009g0188a0001c0002t0024g0183others(8): Show | 15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.677-4655_677-4652d others(6): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16020360 | |||||
| chr17:16020395
|
C | T | 160 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(157): Show | 200 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.677-4622C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020395 | ||||||
| chr17:16020460
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.677-4557G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020460 | ||||||
| chr17:16020560
|
A | C | 8 | a0001c0001t0010g0007a0001c0001t0010g0177a0001c0001t0010g0178others(5): Show | 10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.677-4457A>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020560 | ||||||
| chr17:16020575
|
A | C | 2 | a0001c0001t0020g0008a0001c0001t0029g0008 | 5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-4442A>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020575 | ||||||
| chr17:16020606
|
T | A | 1 | a0001c0001t0043g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.677-4411T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020606 | ||||||
| chr17:16020667
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG01099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.677-4350C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020667 | ||||||
| chr17:16020776
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.677-4241G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020776 | ||||||
| chr17:16020860
|
T | C | 18 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(15): Show | 24 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.677-4157T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020860 | ||||||
| chr17:16020978
|
C | T | 4 | a0001c0001t0003g0013a0001c0001t0003g0103a0001c0001t0045g0013others(1): Show | 5 | HG01192.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-4039C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020978 | ||||||
| chr17:16021008
|
GTTCA | G | 7 | a0001c0001t0010g0007a0001c0001t0010g0177a0001c0001t0010g0178others(4): Show | 9 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-4000_677-3997d others(6): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16021008 | |||||
| chr17:16021056
|
A | G | 163 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(160): Show | 203 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.677-3961A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021056 | ||||||
| chr17:16021094
|
T | C | 4 | a0001c0001t0016g0030a0001c0001t0016g0162a0001c0001t0027g0169others(1): Show | 5 | HG01891.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-3923T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021094 | ||||||
| chr17:16021109
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.677-3908T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021109 | ||||||
| chr17:16021401
|
CA | C | 2 | a0001c0001t0020g0008a0001c0001t0029g0008 | 5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-3609delA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16021401 | |||||
| chr17:16021409
|
C | G | 3 | a0001c0001t0031g0090a0001c0001t0031g0125a0001c0001t0059g0091 | 3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.677-3608C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021409 | ||||||
| chr17:16021478
|
T | C | 1 | a0001c0001t0060g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.677-3539T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021478 | ||||||
| chr17:16021613
|
G | C | 7 | a0001c0001t0010g0007a0001c0001t0010g0177a0001c0001t0010g0178others(4): Show | 9 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-3404G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021613 | ||||||
| chr17:16021684
|
G | A | 1 | a0001c0001t0063g0159 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.677-3333G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021684 | ||||||
| chr17:16022025
|
G | A | 25 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(22): Show | 32 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.677-2992G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022025 | ||||||
| chr17:16022028
|
G | T | 8 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(5): Show | 13 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-2989G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022028 | ||||||
| chr17:16022038
|
G | A | 2 | a0002c0003t0056g0087a0002c0003t0064g0088 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.677-2979G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022038 | ||||||
| chr17:16022087
|
G | GGGTTGT | 80 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(77): Show | 96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-2926_677-2921d others(8): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16022087 | |||||
| chr17:16022116
|
G | GT | 69 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(66): Show | 89 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.677-2898dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16022116 | |||||
| chr17:16022264
|
T | C | 1 | a0001c0001t0044g0181 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.677-2753T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022264 | ||||||
| chr17:16022362
|
T | A | 1 | a0001c0001t0001g0136 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.677-2655T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022362 | ||||||
| chr17:16022370
|
C | T | 2 | a0002c0003t0056g0087a0002c0003t0064g0088 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.677-2647C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022370 | ||||||
| chr17:16022389
|
C | A | 1 | a0001c0001t0043g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.677-2628C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022389 | ||||||
| chr17:16022420
|
A | G | 80 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(77): Show | 96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-2597A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022420 | ||||||
| chr17:16022460
|
G | C | 8 | a0001c0001t0010g0007a0001c0001t0010g0177a0001c0001t0010g0178others(5): Show | 10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.677-2557G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022460 | ||||||
| chr17:16022464
|
T | C | 1 | a0001c0001t0004g0075 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.677-2553T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022464 | ||||||
| chr17:16022495
|
A | G | 1 | a0001c0001t0011g0022 | 3 | HG02622.hp1 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.677-2522A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022495 | ||||||
| chr17:16022551
|
G | C | 4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG02273.hp2 NA18968.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.677-2466G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022551 | ||||||
| chr17:16022627
|
A | C | 1 | a0001c0002t0025g0186 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.677-2390A>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022627 | ||||||
| chr17:16022719
|
T | C | 80 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(77): Show | 96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-2298T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022719 | ||||||
| chr17:16022933
|
G | A | 4 | a0001c0001t0004g0020a0001c0001t0005g0020a0001c0001t0005g0066others(1): Show | 4 | HG00621.hp2 NA18982.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.677-2084G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022933 | ||||||
| chr17:16023007
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.677-2010T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023007 | ||||||
| chr17:16023049
|
G | C | 69 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(66): Show | 89 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.677-1968G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023049 | ||||||
| chr17:16023074
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0002g0039 | 2 | NA18982.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.677-1943A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023074 | ||||||
| chr17:16023155
|
C | T | 1 | a0002c0003t0064g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.677-1862C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023155 | ||||||
| chr17:16023467
|
G | C | 22 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(19): Show | 28 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.677-1550G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023467 | ||||||
| chr17:16023521
|
C | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(22): Show | 31 | HG01192.hp2 HG02109.hp1 HG02451.hp1 others(28): Show |
intron_variant | MODIFIER | c.677-1496C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023521 | ||||||
| chr17:16023548
|
A | G | 8 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(5): Show | 13 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-1469A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023548 | ||||||
| chr17:16023561
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.677-1456G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023561 | ||||||
| chr17:16023563
|
G | A | 5 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(2): Show | 7 | HG01891.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.677-1454G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023563 | ||||||
| chr17:16023649
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.677-1368A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023649 | ||||||
| chr17:16023741
|
CTCAAAGA others(3): Show |
C | 10 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(7): Show | 14 | HG03491.hp1 HG03654.hp2 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.677-1274_677-1265d others(12): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16023741 | |||||
| chr17:16023775
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0003g0098a0001c0001t0003g0107 | 3 | HG02809.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.677-1242G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023775 | ||||||
| chr17:16023909
|
C | A | 162 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(159): Show | 202 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.677-1108C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023909 | ||||||
| chr17:16024228
|
G | A | 24 | a0001c0001t0001g0165a0001c0001t0006g0017a0001c0001t0006g0023others(21): Show | 31 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.677-789G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024228 | ||||||
| chr17:16024290
|
CTTTTTTT others(3): Show |
C | 80 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(77): Show | 96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-713_677-704del others(10): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16024290 | |||||
| chr17:16024364
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.677-653C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024364 | ||||||
| chr17:16024462
|
A | AT | 44 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(41): Show | 55 | HG00621.hp1 HG01109.hp2 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.677-539dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16024462 | |||||
| chr17:16024462
|
A | ATT | 14 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0042g0179others(11): Show | 20 | HG01884.hp1 HG01934.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.677-540_677-539dup others(2): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16024462 | |||||
| chr17:16024462
|
A | ATTTT | 74 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(71): Show | 89 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.677-542_677-539dup others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16024462 | |||||
| chr17:16024462
|
A | ATTTTT | 5 | a0001c0001t0004g0082a0001c0001t0008g0073a0001c0001t0015g0029others(2): Show | 6 | HG00735.hp2 HG02027.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.677-543_677-539dup others(5): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16024462 | |||||
| chr17:16024495
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.677-522C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024495 | ||||||
| chr17:16024551
|
C | T | 1 | a0001c0001t0019g0163 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.677-466C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024551 | ||||||
| chr17:16024610
|
G | A | 1 | a0001c0001t0001g0126 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.677-407G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024610 | ||||||
| chr17:16024754
|
A | G | 1 | a0001c0001t0043g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.677-263A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024754 | ||||||
| chr17:16024864
|
T | C | 8 | a0001c0001t0011g0022a0001c0001t0011g0032a0001c0001t0011g0092others(5): Show | 13 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-153T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024864 | ||||||
| chr17:16024901
|
T | C | 8 | a0001c0001t0010g0007a0001c0001t0010g0177a0001c0001t0010g0178others(5): Show | 10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.677-116T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024901 | ||||||
| chr17:16024908
|
T | C | 38 | a0001c0001t0003g0098a0001c0001t0004g0019a0001c0001t0004g0020others(35): Show | 44 | HG00408.hp1 HG00621.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.677-109T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024908 | ||||||
| chr17:16024975
|
C | G | 1 | a0001c0001t0005g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.677-42C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024975 | ||||||
| chr17:16025270
|
T | G | 117 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0038others(114): Show | 145 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.831+99T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025270 | ||||||
| chr17:16025286
|
G | C | 99 | a0001c0001t0001g0038a0001c0001t0003g0013a0001c0001t0003g0103others(96): Show | 123 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.831+115G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025286 | ||||||
| chr17:16025288
|
C | A | 2 | a0001c0001t0031g0090a0001c0001t0059g0091 | 2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.831+117C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025288 | ||||||
| chr17:16025519
|
C | T | 20 | a0001c0001t0006g0017a0001c0001t0006g0023a0001c0001t0006g0167others(17): Show | 26 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.831+348C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025519 | ||||||
| chr17:16025571
|
A | G | 95 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(92): Show | 118 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.831+400A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025571 | ||||||
| chr17:16025676
|
A | T | 5 | a0001c0001t0006g0023a0001c0001t0006g0167a0001c0001t0006g0176others(2): Show | 6 | HG02015.hp2 HG04184.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+505A>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025676 | ||||||
| chr17:16025689
|
C | A | 50 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(47): Show | 65 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.831+518C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025689 | ||||||
| chr17:16025715
|
G | A | 1 | a0004c0005t0004g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.831+544G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025715 | ||||||
| chr17:16025822
|
A | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0112a0001c0001t0001g0124others(5): Show | 11 | HG00408.hp2 HG00673.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+651A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025822 | ||||||
| chr17:16025842
|
G | C | 4 | a0001c0001t0016g0030a0001c0001t0016g0162a0001c0001t0027g0169others(1): Show | 5 | HG01891.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+671G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025842 | ||||||
| chr17:16025903
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00621.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.832-637T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025903 | ||||||
| chr17:16026086
|
C | A | 1 | a0001c0001t0057g0106 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.832-454C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16026086 | ||||||
| chr17:16026146
|
C | A | 2 | a0001c0001t0001g0147a0001c0001t0002g0146 | 2 | HG00673.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.832-394C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16026146 | ||||||
| chr17:16026153
|
A | AT | 80 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(77): Show | 96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.832-386dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 16026153 | |||||
| chr17:16026272
|
T | C | 1 | a0001c0001t0048g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.832-268T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16026272 | ||||||
| chr17:16026322
|
T | C | 6 | a0001c0001t0006g0017a0001c0001t0006g0042a0001c0001t0006g0170others(3): Show | 9 | HG00741.hp1 HG01433.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.832-218T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16026322 | ||||||
| chr17:16026773
|
G | A | 135 | a0001c0001t0004g0002a0001c0001t0004g0011a0001c0001t0004g0012others(132): Show | 169 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.994+71G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 9/9 | chr17 | 16026773 | ||||||
| chr17:16026819
|
A | G | 32 | a0001c0001t0006g0017a0001c0001t0006g0023a0001c0001t0006g0042others(29): Show | 41 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.994+117A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 9/9 | chr17 | 16026819 | ||||||
| chr17:16026833
|
T | C | 1 | a0001c0001t0015g0069 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.994+131T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 9/9 | chr17 | 16026833 | ||||||
| chr17:16026944
|
C | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0109a0001c0001t0002g0035 | 3 | NA18961.hp2 NA18999.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.994+242C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 9/9 | chr17 | 16026944 |