| geneid | 63923 |
|---|---|
| ensemblid | ENSG00000120332.17 |
| hgncid | 22942 |
| symbol | TNN |
| name | tenascin N |
| refseq_nuc | NM_022093.2 |
| refseq_prot | NP_071376.1 |
| ensembl_nuc | ENST00000239462.9 |
| ensembl_prot | ENSP00000239462.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 175067833 |
| end | 175148075 |
| strand | + |
| ver | v1.2 |
| region | chr1:175067833-175148075 |
| region5000 | chr1:175062833-175153075 |
| regionname0 | TNN_chr1_175067833_175148075 |
| regionname5000 | TNN_chr1_175062833_175153075 |
| 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 | 0/0 | 1299 | 52 | 25 | 11 | 5 | 4 | 7 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002 | 0/0 | 1299 | 41 | 24 | 6 | 4 | 4 | 3 | 2 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0003 | 0/0 | 1299 | 34 | 1 | 0 | 26 | 2 | 5 | 24 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004 | 1/1 | 1299 | 24 | 1 | 4 | 15 | 0 | 2 | 11 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0005 | 0/0 | 1299 | 24 | 0 | 7 | 17 | 0 | 0 | 14 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0006 | 0/0 | 1299 | 21 | 0 | 8 | 10 | 0 | 3 | 7 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0007 | 0/0 | 1299 | 20 | 10 | 1 | 3 | 1 | 5 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0008 | 0/0 | 1299 | 18 | 0 | 0 | 16 | 1 | 1 | 13 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0009 | 0/0 | 1299 | 14 | 0 | 3 | 5 | 2 | 4 | 5 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0010 | 0/0 | 1299 | 13 | 1 | 4 | 8 | 0 | 0 | 6 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0011 | 0/0 | 1299 | 11 | 0 | 5 | 5 | 1 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0012 | 0/0 | 1299 | 9 | 0 | 1 | 8 | 0 | 0 | 6 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0013 | 0/0 | 1299 | 8 | 6 | 1 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0014 | 0/0 | 1299 | 7 | 3 | 0 | 3 | 0 | 1 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0015 | 0/0 | 1299 | 7 | 1 | 2 | 1 | 0 | 3 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0016 | 0/0 | 1299 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0017 | 0/0 | 1299 | 5 | 0 | 2 | 3 | 0 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0018 | 0/0 | 1299 | 5 | 0 | 0 | 4 | 0 | 1 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0019 | 0/0 | 1299 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0020 | 0/0 | 1299 | 4 | 0 | 0 | 3 | 0 | 1 | 2 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0021 | 0/0 | 1299 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0022 | 0/0 | 1299 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0023 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0024 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0025 | 0/0 | 1299 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0026 | 0/0 | 1299 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0027 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0028 | 0/0 | 1299 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0029 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0030 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0031 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0032 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0033 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0034 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0035 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0036 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0037 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0038 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0039 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0040 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0041 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0042 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0043 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0044 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0045 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0046 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0047 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0048 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0049 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0050 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0051 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0052 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0053 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0054 | 0/0 | 1211 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0055 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0056 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0057 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0058 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| 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 | 0/0 | 3900 | 32 | 12 | 8 | 4 | 3 | 5 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0002 | 0/0 | 3900 | 25 | 1 | 0 | 18 | 1 | 5 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0003 | 0/0 | 3900 | 22 | 0 | 7 | 15 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0004 | 0/0 | 3900 | 18 | 0 | 7 | 8 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0005 | 0/0 | 3900 | 16 | 4 | 3 | 4 | 3 | 2 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0006 | 0/0 | 3900 | 16 | 8 | 1 | 3 | 1 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0007 | 0/0 | 3900 | 16 | 0 | 0 | 14 | 1 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0008 | 0/0 | 3900 | 15 | 0 | 2 | 12 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0009 | 0/0 | 3900 | 15 | 12 | 1 | 0 | 1 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0010 | 0/0 | 3900 | 12 | 1 | 4 | 7 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0011 | 0/0 | 3900 | 11 | 0 | 5 | 5 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0012 | 0/0 | 3900 | 9 | 0 | 1 | 4 | 0 | 4 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0013 | 0/0 | 3900 | 9 | 0 | 1 | 8 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0014 | 0/0 | 3900 | 8 | 6 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0015 | 0/0 | 3900 | 7 | 0 | 0 | 7 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0016 | 0/0 | 3900 | 6 | 4 | 1 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0017 | 0/0 | 3900 | 6 | 0 | 2 | 1 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0018 | 0/0 | 3900 | 5 | 0 | 0 | 4 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0019 | 0/0 | 3900 | 5 | 1 | 1 | 2 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0020 | 0/0 | 3900 | 5 | 0 | 0 | 5 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0021 | 0/0 | 3900 | 4 | 0 | 2 | 0 | 2 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0022 | 0/0 | 3900 | 4 | 0 | 0 | 3 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0023 | 0/0 | 3900 | 4 | 4 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0024 | 0/0 | 3900 | 4 | 3 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0025 | 0/0 | 3900 | 4 | 0 | 1 | 3 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0026 | 0/0 | 3900 | 4 | 2 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0027 | 0/0 | 3900 | 3 | 0 | 0 | 0 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0028 | 0/0 | 3900 | 3 | 3 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0029 | 0/0 | 3900 | 3 | 3 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0030 | 0/0 | 3900 | 3 | 0 | 0 | 2 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0031 | 0/0 | 3900 | 3 | 2 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0032 | 1/0 | 3900 | 2 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0033 | 0/0 | 3900 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0034 | 0/0 | 3900 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0035 | 0/0 | 3900 | 2 | 0 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0036 | 0/0 | 3900 | 2 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0037 | 0/0 | 3900 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0038 | 0/0 | 3900 | 2 | 1 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0039 | 0/0 | 3900 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0040 | 0/0 | 3900 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0041 | 0/0 | 3900 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0042 | 0/0 | 3900 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0043 | 0/0 | 3900 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0044 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0045 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0046 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0047 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0048 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0049 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0050 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0051 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0052 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0053 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0054 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0055 | 0/1 | 3900 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0056 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0057 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0058 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0059 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0060 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0061 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0062 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0063 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0064 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0065 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0066 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0067 | 0/0 | 3636 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0068 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0069 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0070 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0071 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0072 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0073 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0074 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0075 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0076 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0077 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0078 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0079 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0080 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0081 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0082 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0083 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0084 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0085 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0086 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0087 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0088 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0089 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0090 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0091 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0092 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0093 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0094 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0095 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| c0096 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| 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 | 0/1 | 1143 | 261 | 63 | 51 | 104 | 11 | 31 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0002 | 1/0 | 1143 | 54 | 0 | 4 | 37 | 4 | 8 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0003 | 0/0 | 1143 | 33 | 13 | 8 | 9 | 1 | 2 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0004 | 0/0 | 1143 | 5 | 5 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0005 | 0/0 | 1143 | 4 | 3 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0006 | 0/0 | 1143 | 3 | 2 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0007 | 0/0 | 1143 | 3 | 3 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0008 | 0/0 | 1143 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0009 | 0/0 | 1143 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0010 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0011 | 0/0 | 1143 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0012 | 0/0 | 1143 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0013 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0014 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0015 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| t0016 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0204 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| 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 | 0/0 | 3900 | 32 | 12 | 8 | 4 | 3 | 5 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0016 | 0/0 | 3900 | 6 | 4 | 1 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0028 | 0/0 | 3900 | 3 | 3 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0031 | 0/0 | 3900 | 3 | 2 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0036 | 0/0 | 3900 | 2 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0042 | 0/0 | 3900 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0074 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0082 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0083 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0089 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0005 | 0/0 | 3900 | 16 | 4 | 3 | 4 | 3 | 2 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0009 | 0/0 | 3900 | 15 | 12 | 1 | 0 | 1 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0026 | 0/0 | 3900 | 4 | 2 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0029 | 0/0 | 3900 | 3 | 3 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0037 | 0/0 | 3900 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0079 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0003c0002 | 0/0 | 3900 | 25 | 1 | 0 | 18 | 1 | 5 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0003c0015 | 0/0 | 3900 | 7 | 0 | 0 | 7 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0003c0047 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0003c0048 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004c0008 | 0/0 | 3900 | 15 | 0 | 2 | 12 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004c0019 | 0/0 | 3900 | 5 | 1 | 1 | 2 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004c0032 | 1/0 | 3900 | 2 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004c0055 | 0/1 | 3900 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004c0056 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0005c0003 | 0/0 | 3900 | 22 | 0 | 7 | 15 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0005c0057 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0005c0061 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0006c0004 | 0/0 | 3900 | 18 | 0 | 7 | 8 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0006c0044 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0006c0062 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0006c0063 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0007c0006 | 0/0 | 3900 | 16 | 8 | 1 | 3 | 1 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0007c0038 | 0/0 | 3900 | 2 | 1 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0007c0073 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0007c0081 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0008c0007 | 0/0 | 3900 | 16 | 0 | 0 | 14 | 1 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0008c0040 | 0/0 | 3900 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0009c0012 | 0/0 | 3900 | 9 | 0 | 1 | 4 | 0 | 4 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0009c0021 | 0/0 | 3900 | 4 | 0 | 2 | 0 | 2 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0009c0050 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0010c0010 | 0/0 | 3900 | 12 | 1 | 4 | 7 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0010c0076 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0011c0011 | 0/0 | 3900 | 11 | 0 | 5 | 5 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0012c0013 | 0/0 | 3900 | 9 | 0 | 1 | 8 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0013c0014 | 0/0 | 3900 | 8 | 6 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0014c0024 | 0/0 | 3900 | 4 | 3 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0014c0030 | 0/0 | 3900 | 3 | 0 | 0 | 2 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0015c0017 | 0/0 | 3900 | 6 | 0 | 2 | 1 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0015c0092 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0016c0020 | 0/0 | 3900 | 5 | 0 | 0 | 5 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0017c0025 | 0/0 | 3900 | 4 | 0 | 1 | 3 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0017c0075 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0018c0018 | 0/0 | 3900 | 5 | 0 | 0 | 4 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0019c0023 | 0/0 | 3900 | 4 | 4 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0020c0022 | 0/0 | 3900 | 4 | 0 | 0 | 3 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0021c0027 | 0/0 | 3900 | 3 | 0 | 0 | 0 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0022c0058 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0022c0059 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0022c0060 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0023c0043 | 0/0 | 3900 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0024c0039 | 0/0 | 3900 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0025c0041 | 0/0 | 3900 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0026c0035 | 0/0 | 3900 | 2 | 0 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0027c0034 | 0/0 | 3900 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0028c0033 | 0/0 | 3900 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0029c0096 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0030c0095 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0031c0068 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0032c0093 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0033c0072 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0034c0070 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0035c0071 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0036c0090 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0037c0080 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0038c0069 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0039c0078 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0040c0077 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0041c0085 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0042c0084 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0043c0086 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0044c0087 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0045c0088 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0046c0091 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0047c0045 | 0/0 | 3900 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0048c0046 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0049c0053 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0050c0054 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0051c0066 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0052c0064 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0053c0065 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0054c0067 | 0/0 | 3636 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0055c0049 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0056c0052 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0057c0051 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0058c0094 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5042 | 30 | 12 | 8 | 4 | 1 | 5 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0001t0002 | 0/0 | 5042 | 2 | 0 | 0 | 0 | 2 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0016t0001 | 0/0 | 5042 | 5 | 3 | 1 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0016t0008 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0028t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0028t0007 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0031t0005 | 0/0 | 5042 | 3 | 2 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0036t0001 | 0/0 | 5042 | 2 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0042t0001 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0074t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0082t0008 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0083t0001 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0001c0089t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0005t0001 | 0/0 | 5042 | 3 | 1 | 0 | 0 | 2 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0005t0002 | 0/0 | 5042 | 5 | 0 | 0 | 3 | 1 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0005t0003 | 0/0 | 5042 | 5 | 1 | 3 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0005t0004 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0005t0007 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0005t0016 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0009t0001 | 0/0 | 5042 | 9 | 9 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0009t0002 | 0/0 | 5042 | 2 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0009t0003 | 0/0 | 5042 | 3 | 2 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0009t0013 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0026t0001 | 0/0 | 5042 | 2 | 0 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0026t0003 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0029t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0029t0003 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0037t0003 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0002c0079t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0003c0002t0001 | 0/0 | 5042 | 24 | 1 | 0 | 18 | 1 | 4 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0003c0002t0012 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0003c0015t0001 | 0/0 | 5042 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0003c0015t0003 | 0/0 | 5042 | 5 | 0 | 0 | 5 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0003c0047t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0003c0048t0001 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004c0008t0001 | 0/0 | 5042 | 3 | 0 | 0 | 3 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004c0008t0002 | 0/0 | 5042 | 10 | 0 | 0 | 9 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004c0008t0003 | 0/0 | 5042 | 2 | 0 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004c0019t0001 | 0/0 | 5042 | 4 | 1 | 1 | 1 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004c0019t0002 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004c0032t0002 | 1/0 | 5042 | 2 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004c0055t0001 | 0/1 | 5042 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0004c0056t0002 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0005c0003t0001 | 0/0 | 5042 | 19 | 0 | 6 | 13 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0005c0003t0002 | 0/0 | 5042 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0005c0003t0003 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0005c0057t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0005c0061t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0006c0004t0001 | 0/0 | 5042 | 17 | 0 | 7 | 7 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0006c0004t0002 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0006c0044t0014 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0006c0062t0003 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0006c0063t0002 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0007c0006t0001 | 0/0 | 5042 | 14 | 6 | 1 | 3 | 1 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0007c0006t0004 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0007c0006t0015 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0007c0038t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0007c0038t0011 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0007c0073t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0007c0081t0003 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0008c0007t0001 | 0/0 | 5042 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0008c0007t0002 | 0/0 | 5042 | 14 | 0 | 0 | 12 | 1 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0008c0040t0003 | 0/0 | 5042 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0009c0012t0002 | 0/0 | 5042 | 8 | 0 | 0 | 4 | 0 | 4 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0009c0012t0003 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0009c0021t0001 | 0/0 | 5042 | 4 | 0 | 2 | 0 | 2 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0009c0050t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0010c0010t0001 | 0/0 | 5042 | 12 | 1 | 4 | 7 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0010c0076t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0011c0011t0001 | 0/0 | 5042 | 10 | 0 | 5 | 4 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0011c0011t0003 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0012c0013t0001 | 0/0 | 5042 | 9 | 0 | 1 | 8 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0013c0014t0001 | 0/0 | 5042 | 8 | 6 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0014c0024t0001 | 0/0 | 5042 | 3 | 3 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0014c0024t0002 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0014c0030t0001 | 0/0 | 5042 | 3 | 0 | 0 | 2 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0015c0017t0001 | 0/0 | 5042 | 6 | 0 | 2 | 1 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0015c0092t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0016c0020t0001 | 0/0 | 5042 | 5 | 0 | 0 | 5 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0017c0025t0001 | 0/0 | 5042 | 4 | 0 | 1 | 3 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0017c0075t0001 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0018c0018t0001 | 0/0 | 5042 | 5 | 0 | 0 | 4 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0019c0023t0001 | 0/0 | 5042 | 4 | 4 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0020c0022t0001 | 0/0 | 5042 | 4 | 0 | 0 | 3 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0021c0027t0001 | 0/0 | 5042 | 3 | 0 | 0 | 0 | 0 | 3 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0022c0058t0006 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0022c0059t0001 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0022c0060t0006 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0023c0043t0001 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0024c0039t0009 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0025c0041t0002 | 0/0 | 5042 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0026c0035t0001 | 0/0 | 5042 | 2 | 0 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0027c0034t0003 | 0/0 | 5042 | 2 | 2 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0028c0033t0001 | 0/0 | 5042 | 2 | 0 | 0 | 2 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0029c0096t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0030c0095t0003 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0031c0068t0006 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0032c0093t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0033c0072t0004 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0034c0070t0004 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0035c0071t0004 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0036c0090t0005 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0037c0080t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0038c0069t0002 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0039c0078t0003 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0040c0077t0001 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0041c0085t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0042c0084t0001 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0043c0086t0001 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0044c0087t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0045c0088t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0046c0091t0003 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0047c0045t0001 | 0/0 | 5042 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0048c0046t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0049c0053t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0050c0054t0001 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0051c0066t0010 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0052c0064t0001 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0053c0065t0001 | 0/0 | 5042 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0054c0067t0001 | 0/0 | 4778 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0055c0049t0002 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0056c0052t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0057c0051t0001 | 0/0 | 5042 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| a0058c0094t0001 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | copy fasta | chr1 | 175062833 | 175153075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0016t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0016t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0016t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0016t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0016t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0016t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0028t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0028t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0028t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0031t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0031t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0031t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0036t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0036t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0042t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0042t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0074t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0082t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0083t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0001c0089t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0005t0016g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0003g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0003g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0003g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0009t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0026t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0026t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0026t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0029t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0029t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0029t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0037t0003g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0037t0003g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0002c0079t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0002t0012g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0015t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0015t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0015t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0015t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0015t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0015t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0015t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0047t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0003c0048t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0008t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0019t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0019t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0019t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0019t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0019t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0032t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0032t0002g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0055t0001g0204 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0004c0056t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0003t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0057t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0005c0061t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0004t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0044t0014g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0062t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0006c0063t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0006t0015g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0038t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0038t0011g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0073t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0007c0081t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0007t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0040t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0008c0040t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0009c0012t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0009c0012t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0009c0012t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0009c0012t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0009c0012t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0009c0012t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0009c0012t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0009c0012t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0009c0021t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0009c0021t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0009c0021t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0009c0021t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0009c0050t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0010c0010t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0010c0010t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0010c0010t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0010c0010t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0010c0010t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0010c0010t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0010c0010t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0010c0010t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0010c0010t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0010c0010t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0010c0010t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0010c0010t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0010c0076t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0011c0011t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0011c0011t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0011c0011t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0011c0011t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0011c0011t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0011c0011t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0011c0011t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0011c0011t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0011c0011t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0011c0011t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0011c0011t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0012c0013t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0012c0013t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0012c0013t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0012c0013t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0012c0013t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0012c0013t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0012c0013t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0012c0013t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0012c0013t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0013c0014t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0013c0014t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0013c0014t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0013c0014t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0013c0014t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0013c0014t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0013c0014t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0013c0014t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0014c0024t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0014c0024t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0014c0024t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0014c0024t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0014c0030t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0014c0030t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0014c0030t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0015c0017t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0015c0017t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0015c0017t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0015c0017t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0015c0017t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0015c0092t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0016c0020t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0016c0020t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0016c0020t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0016c0020t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0016c0020t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0017c0025t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0017c0025t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0017c0025t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0017c0025t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0017c0075t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0018c0018t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0018c0018t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0018c0018t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0018c0018t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0018c0018t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0019c0023t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0019c0023t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0019c0023t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0019c0023t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0020c0022t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0020c0022t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0020c0022t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0020c0022t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0021c0027t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0021c0027t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0021c0027t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0022c0058t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0022c0059t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0022c0060t0006g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0023c0043t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0023c0043t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0024c0039t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0024c0039t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0025c0041t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0025c0041t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0026c0035t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0026c0035t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0027c0034t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0027c0034t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0028c0033t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0028c0033t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0029c0096t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0030c0095t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0031c0068t0006g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0032c0093t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0033c0072t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0034c0070t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0035c0071t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0036c0090t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0037c0080t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0038c0069t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0039c0078t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0040c0077t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0041c0085t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0042c0084t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0043c0086t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0044c0087t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0045c0088t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0046c0091t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0047c0045t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0048c0046t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0049c0053t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0050c0054t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0051c0066t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0052c0064t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0053c0065t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0054c0067t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0055c0049t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0056c0052t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0057c0051t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| a0058c0094t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0122 | EUR | GBR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00099 | hp2 | a0007 | c0006 | t0001 | g0339 | EUR | GBR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00140 | hp1 | a0002 | c0005 | t0001 | g0119 | EUR | GBR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00140 | hp2 | a0008 | c0007 | t0002 | g0099 | EUR | GBR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00280 | hp1 | a0003 | c0002 | t0001 | g0278 | EUR | FIN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00280 | hp2 | a0011 | c0011 | t0001 | g0215 | EUR | FIN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00323 | hp1 | a0003 | c0048 | t0001 | g0293 | EUR | FIN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00323 | hp2 | a0002 | c0005 | t0001 | g0121 | EUR | FIN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00408 | hp1 | a0011 | c0011 | t0001 | g0238 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00408 | hp2 | a0010 | c0010 | t0001 | g0090 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00438 | hp1 | a0002 | c0005 | t0016 | g0030 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00438 | hp2 | a0006 | c0004 | t0001 | g0253 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00544 | hp1 | a0018 | c0018 | t0001 | g0290 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00544 | hp2 | a0008 | c0007 | t0002 | g0130 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00609 | hp1 | a0003 | c0002 | t0001 | g0303 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00609 | hp2 | a0025 | c0041 | t0002 | g0092 | EAS | CHS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00639 | hp1 | a0009 | c0021 | t0001 | g0004 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00639 | hp2 | a0011 | c0011 | t0001 | g0221 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00642 | hp1 | a0004 | c0032 | t0002 | g0192 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00642 | hp2 | a0042 | c0084 | t0001 | g0079 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00738 | hp1 | a0026 | c0035 | t0001 | g0216 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG00738 | hp2 | a0006 | c0004 | t0001 | g0191 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01069 | hp1 | a0022 | c0059 | t0001 | g0175 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01069 | hp2 | a0006 | c0004 | t0001 | g0244 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01070 | hp1 | a0047 | c0045 | t0001 | g0207 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01070 | hp2 | a0002 | c0026 | t0001 | g0001 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01071 | hp1 | a0002 | c0026 | t0001 | g0001 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01071 | hp2 | a0006 | c0004 | t0001 | g0245 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01074 | hp1 | a0006 | c0063 | t0002 | g0217 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01081 | hp1 | a0038 | c0069 | t0002 | g0034 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01106 | hp2 | a0001 | c0036 | t0001 | g0341 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01109 | hp1 | a0015 | c0017 | t0001 | g0127 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01109 | hp2 | a0009 | c0012 | t0003 | g0273 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01167 | hp1 | a0007 | c0006 | t0001 | g0349 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01167 | hp2 | a0011 | c0011 | t0001 | g0220 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01168 | hp1 | a0011 | c0011 | t0001 | g0190 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01168 | hp2 | a0002 | c0009 | t0002 | g0363 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01192 | hp1 | a0002 | c0005 | t0003 | g0103 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01192 | hp2 | a0001 | c0083 | t0001 | g0159 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01243 | hp1 | a0017 | c0025 | t0001 | g0109 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01243 | hp2 | a0017 | c0075 | t0001 | g0035 | AMR | PUR | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01255 | hp2 | a0005 | c0003 | t0001 | g0212 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01256 | hp1 | a0006 | c0004 | t0001 | g0182 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01256 | hp2 | a0005 | c0003 | t0001 | g0169 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01257 | hp1 | a0010 | c0010 | t0001 | g0110 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01257 | hp2 | a0012 | c0013 | t0001 | g0101 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01258 | hp1 | a0010 | c0010 | t0001 | g0112 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01258 | hp2 | a0005 | c0003 | t0001 | g0181 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01261 | hp1 | a0054 | c0067 | t0001 | g0250 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01261 | hp2 | a0001 | c0016 | t0001 | g0358 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01346 | hp1 | a0006 | c0004 | t0001 | g0243 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01358 | hp1 | a0013 | c0014 | t0001 | g0056 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01358 | hp2 | a0009 | c0021 | t0001 | g0276 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0351 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01361 | hp2 | a0005 | c0003 | t0001 | g0257 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01433 | hp1 | a0011 | c0011 | t0001 | g0260 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01433 | hp2 | a0004 | c0008 | t0003 | g0247 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01496 | hp1 | a0006 | c0004 | t0001 | g0251 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01496 | hp2 | a0015 | c0017 | t0001 | g0002 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01515 | hp1 | a0009 | c0021 | t0001 | g0271 | EUR | IBS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01515 | hp2 | a0002 | c0005 | t0002 | g0116 | EUR | IBS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01517 | hp1 | a0009 | c0021 | t0001 | g0272 | EUR | IBS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01517 | hp2 | a0001 | c0016 | t0001 | g0356 | EUR | IBS | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01884 | hp1 | a0001 | c0031 | t0005 | g0156 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01891 | hp1 | a0002 | c0005 | t0004 | g0008 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01891 | hp2 | a0013 | c0014 | t0001 | g0060 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01928 | hp1 | a0010 | c0010 | t0001 | g0113 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01928 | hp2 | a0005 | c0003 | t0001 | g0176 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01934 | hp1 | a0005 | c0003 | t0003 | g0256 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01934 | hp2 | a0010 | c0010 | t0001 | g0111 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01943 | hp1 | a0031 | c0068 | t0006 | g0100 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01943 | hp2 | a0002 | c0005 | t0003 | g0106 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01975 | hp1 | a0046 | c0091 | t0003 | g0104 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01975 | hp2 | a0004 | c0019 | t0001 | g0353 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01978 | hp1 | a0005 | c0003 | t0001 | g0186 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01978 | hp2 | a0004 | c0008 | t0003 | g0246 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01993 | hp1 | a0026 | c0035 | t0001 | g0214 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01993 | hp2 | a0002 | c0005 | t0003 | g0105 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02015 | hp1 | a0012 | c0013 | t0001 | g0082 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02015 | hp2 | a0004 | c0008 | t0001 | g0228 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02040 | hp1 | a0028 | c0033 | t0001 | g0236 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02040 | hp2 | a0010 | c0010 | t0001 | g0077 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02055 | hp1 | a0053 | c0065 | t0001 | g0268 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02055 | hp2 | a0002 | c0009 | t0001 | g0047 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02071 | hp1 | a0008 | c0007 | t0002 | g0058 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02083 | hp1 | a0011 | c0011 | t0003 | g0189 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02083 | hp2 | a0006 | c0004 | t0001 | g0249 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02129 | hp1 | a0056 | c0052 | t0001 | g0282 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02129 | hp2 | a0004 | c0056 | t0002 | g0193 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02132 | hp1 | a0005 | c0003 | t0001 | g0232 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02132 | hp2 | a0008 | c0007 | t0002 | g0142 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02135 | hp1 | a0004 | c0019 | t0002 | g0237 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02135 | hp2 | a0002 | c0005 | t0002 | g0342 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02145 | hp1 | a0022 | c0060 | t0006 | g0316 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02145 | hp2 | a0044 | c0087 | t0001 | g0335 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02155 | hp1 | a0005 | c0003 | t0001 | g0188 | EAS | CDX | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02155 | hp2 | a0012 | c0013 | t0001 | g0073 | EAS | CDX | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02165 | hp1 | a0006 | c0004 | t0001 | g0195 | EAS | CDX | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CDX | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02257 | hp1 | a0002 | c0005 | t0003 | g0150 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02257 | hp2 | a0002 | c0009 | t0001 | g0041 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02280 | hp1 | a0007 | c0006 | t0001 | g0337 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02280 | hp2 | a0022 | c0058 | t0006 | g0274 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02300 | hp1 | a0011 | c0011 | t0001 | g0240 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02451 | hp1 | a0024 | c0039 | t0009 | g0012 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02451 | hp2 | a0007 | c0006 | t0001 | g0061 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02523 | hp1 | a0003 | c0002 | t0001 | g0297 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02523 | hp2 | a0004 | c0008 | t0002 | g0206 | EAS | KHV | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02572 | hp1 | a0002 | c0009 | t0003 | g0357 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02572 | hp2 | a0001 | c0074 | t0001 | g0052 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02602 | hp1 | a0003 | c0002 | t0001 | g0279 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02602 | hp2 | a0015 | c0017 | t0001 | g0002 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02615 | hp1 | a0019 | c0023 | t0001 | g0174 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02615 | hp2 | a0001 | c0016 | t0001 | g0355 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02622 | hp1 | a0035 | c0071 | t0004 | g0015 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02622 | hp2 | a0051 | c0066 | t0010 | g0167 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02630 | hp1 | a0002 | c0009 | t0001 | g0036 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02630 | hp2 | a0002 | c0029 | t0003 | g0053 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02647 | hp1 | a0015 | c0092 | t0001 | g0124 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02647 | hp2 | a0002 | c0079 | t0001 | g0095 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02698 | hp1 | a0003 | c0002 | t0012 | g0277 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02698 | hp2 | a0007 | c0006 | t0001 | g0094 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02717 | hp2 | a0002 | c0005 | t0007 | g0057 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02723 | hp1 | a0002 | c0009 | t0003 | g0365 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02723 | hp2 | a0023 | c0043 | t0001 | g0032 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0350 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02735 | hp2 | a0009 | c0012 | t0002 | g0326 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02738 | hp1 | a0007 | c0006 | t0001 | g0153 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02738 | hp2 | a0014 | c0030 | t0001 | g0050 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02809 | hp1 | a0007 | c0073 | t0001 | g0051 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02809 | hp2 | a0002 | c0037 | t0003 | g0366 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02818 | hp1 | a0007 | c0006 | t0004 | g0009 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02886 | hp1 | a0007 | c0006 | t0001 | g0371 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02895 | hp2 | a0007 | c0006 | t0001 | g0006 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02896 | hp1 | a0001 | c0028 | t0007 | g0046 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02897 | hp1 | a0007 | c0006 | t0001 | g0007 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02897 | hp2 | a0001 | c0028 | t0007 | g0044 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02922 | hp1 | a0001 | c0042 | t0001 | g0097 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02922 | hp2 | a0002 | c0009 | t0001 | g0038 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02965 | hp1 | a0029 | c0096 | t0001 | g0308 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02965 | hp2 | a0002 | c0026 | t0003 | g0063 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02970 | hp1 | a0001 | c0016 | t0008 | g0045 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02976 | hp1 | a0001 | c0042 | t0001 | g0059 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02976 | hp2 | a0019 | c0023 | t0001 | g0170 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03041 | hp1 | a0033 | c0072 | t0004 | g0013 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03041 | hp2 | a0030 | c0095 | t0003 | g0307 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03098 | hp1 | a0002 | c0029 | t0003 | g0054 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03098 | hp2 | a0001 | c0028 | t0001 | g0364 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03130 | hp1 | a0002 | c0029 | t0001 | g0055 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03130 | hp2 | a0007 | c0006 | t0015 | g0011 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03139 | hp1 | a0034 | c0070 | t0004 | g0014 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03195 | hp1 | a0014 | c0024 | t0001 | g0161 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03195 | hp2 | a0007 | c0038 | t0001 | g0367 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03209 | hp1 | a0024 | c0039 | t0009 | g0010 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03225 | hp1 | a0036 | c0090 | t0005 | g0102 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03225 | hp2 | a0013 | c0014 | t0001 | g0089 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03239 | hp1 | a0009 | c0012 | t0002 | g0294 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03239 | hp2 | a0004 | c0019 | t0001 | g0209 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03486 | hp1 | a0014 | c0024 | t0001 | g0370 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03486 | hp2 | a0027 | c0034 | t0003 | g0168 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03490 | hp1 | a0009 | c0012 | t0002 | g0003 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03491 | hp2 | a0015 | c0017 | t0001 | g0081 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03492 | hp1 | a0015 | c0017 | t0001 | g0083 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03492 | hp2 | a0009 | c0012 | t0002 | g0003 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03516 | hp2 | a0002 | c0009 | t0013 | g0048 | AFR | ESN | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03540 | hp1 | a0019 | c0023 | t0001 | g0309 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03540 | hp2 | a0032 | c0093 | t0001 | g0157 | AFR | GWD | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03579 | hp1 | a0023 | c0043 | t0001 | g0033 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03579 | hp2 | a0001 | c0016 | t0001 | g0359 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03654 | hp1 | a0003 | c0002 | t0001 | g0283 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03654 | hp2 | a0001 | c0036 | t0001 | g0340 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03669 | hp1 | a0001 | c0031 | t0005 | g0075 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03669 | hp2 | a0006 | c0004 | t0001 | g0205 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03688 | hp1 | a0021 | c0027 | t0001 | g0198 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03688 | hp2 | a0007 | c0038 | t0011 | g0368 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03704 | hp1 | a0018 | c0018 | t0001 | g0275 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03704 | hp2 | a0003 | c0002 | t0001 | g0325 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03710 | hp1 | a0006 | c0004 | t0001 | g0218 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03710 | hp2 | a0057 | c0051 | t0001 | g0311 | SAS | PJL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03831 | hp1 | a0002 | c0009 | t0002 | g0361 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03831 | hp2 | a0040 | c0077 | t0001 | g0348 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03834 | hp1 | a0043 | c0086 | t0001 | g0076 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03834 | hp2 | a0008 | c0007 | t0002 | g0096 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03927 | hp1 | a0021 | c0027 | t0001 | g0219 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03927 | hp2 | a0013 | c0014 | t0001 | g0069 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0352 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03942 | hp2 | a0007 | c0081 | t0003 | g0144 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG04115 | hp1 | a0002 | c0005 | t0003 | g0149 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG04115 | hp2 | a0006 | c0004 | t0001 | g0252 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG04184 | hp1 | a0021 | c0027 | t0001 | g0222 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG04184 | hp2 | a0003 | c0002 | t0001 | g0317 | SAS | BEB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG04199 | hp1 | a0002 | c0005 | t0002 | g0347 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG04199 | hp2 | a0004 | c0008 | t0002 | g0171 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG04204 | hp1 | a0007 | c0006 | t0001 | g0115 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG04228 | hp1 | a0050 | c0054 | t0001 | g0234 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG04228 | hp2 | a0020 | c0022 | t0001 | g0269 | SAS | STU | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18522 | hp1 | a0013 | c0014 | t0001 | g0065 | AFR | YRI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18522 | hp2 | a0002 | c0026 | t0003 | g0062 | AFR | YRI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18612 | hp1 | a0020 | c0022 | t0001 | g0284 | EAS | CHB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18612 | hp2 | a0005 | c0003 | t0001 | g0178 | EAS | CHB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18906 | hp1 | a0002 | c0009 | t0001 | g0049 | AFR | YRI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | YRI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18943 | hp1 | a0012 | c0013 | t0001 | g0135 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18943 | hp2 | a0005 | c0003 | t0002 | g0210 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18944 | hp1 | a0004 | c0008 | t0002 | g0208 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18944 | hp2 | a0003 | c0002 | t0001 | g0322 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18945 | hp1 | a0048 | c0046 | t0001 | g0306 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18945 | hp2 | a0003 | c0002 | t0001 | g0300 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18948 | hp1 | a0006 | c0062 | t0003 | g0233 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18948 | hp2 | a0008 | c0007 | t0002 | g0071 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18950 | hp1 | a0003 | c0002 | t0001 | g0315 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18950 | hp2 | a0008 | c0007 | t0001 | g0154 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18951 | hp1 | a0008 | c0040 | t0003 | g0145 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18951 | hp2 | a0003 | c0002 | t0001 | g0292 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18952 | hp1 | a0005 | c0003 | t0001 | g0187 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18952 | hp2 | a0008 | c0007 | t0002 | g0132 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18954 | hp1 | a0005 | c0003 | t0001 | g0179 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18956 | hp1 | a0028 | c0033 | t0001 | g0183 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18956 | hp2 | a0016 | c0020 | t0001 | g0080 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18957 | hp1 | a0002 | c0005 | t0002 | g0022 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18957 | hp2 | a0011 | c0011 | t0001 | g0197 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18962 | hp1 | a0008 | c0007 | t0002 | g0084 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18962 | hp2 | a0005 | c0003 | t0001 | g0230 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18964 | hp1 | a0005 | c0003 | t0002 | g0211 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18964 | hp2 | a0003 | c0002 | t0001 | g0295 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18966 | hp1 | a0010 | c0010 | t0001 | g0026 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18966 | hp2 | a0005 | c0061 | t0001 | g0259 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18967 | hp1 | a0018 | c0018 | t0001 | g0314 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18967 | hp2 | a0010 | c0010 | t0001 | g0143 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18968 | hp1 | a0008 | c0007 | t0002 | g0072 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18968 | hp2 | a0005 | c0003 | t0001 | g0180 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18969 | hp1 | a0003 | c0015 | t0003 | g0281 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18969 | hp2 | a0004 | c0019 | t0001 | g0223 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18970 | hp1 | a0009 | c0050 | t0001 | g0280 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18970 | hp2 | a0006 | c0004 | t0001 | g0194 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18971 | hp1 | a0015 | c0017 | t0001 | g0086 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18971 | hp2 | a0003 | c0047 | t0001 | g0286 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18973 | hp1 | a0002 | c0005 | t0002 | g0019 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18973 | hp2 | a0045 | c0088 | t0001 | g0114 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18975 | hp1 | a0011 | c0011 | t0001 | g0354 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18975 | hp2 | a0008 | c0007 | t0002 | g0141 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18977 | hp1 | a0003 | c0015 | t0003 | g0265 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18977 | hp2 | a0058 | c0094 | t0001 | g0227 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18980 | hp1 | a0009 | c0012 | t0002 | g0301 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18980 | hp2 | a0012 | c0013 | t0001 | g0134 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18981 | hp1 | a0003 | c0015 | t0003 | g0261 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18981 | hp2 | a0010 | c0076 | t0001 | g0152 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18982 | hp1 | a0016 | c0020 | t0001 | g0126 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18982 | hp2 | a0014 | c0024 | t0002 | g0021 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18983 | hp1 | a0003 | c0015 | t0003 | g0263 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18983 | hp2 | a0001 | c0089 | t0001 | g0024 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18985 | hp1 | a0010 | c0010 | t0001 | g0028 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18985 | hp2 | a0020 | c0022 | t0001 | g0298 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18986 | hp1 | a0014 | c0030 | t0001 | g0016 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18986 | hp2 | a0008 | c0007 | t0002 | g0064 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18988 | hp1 | a0003 | c0002 | t0001 | g0310 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18988 | hp2 | a0005 | c0003 | t0001 | g0202 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18989 | hp1 | a0016 | c0020 | t0001 | g0085 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18989 | hp2 | a0018 | c0018 | t0001 | g0320 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18990 | hp1 | a0008 | c0007 | t0001 | g0087 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18990 | hp2 | a0003 | c0002 | t0001 | g0285 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18991 | hp1 | a0041 | c0085 | t0001 | g0088 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18991 | hp2 | a0010 | c0010 | t0001 | g0025 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18992 | hp1 | a0025 | c0041 | t0002 | g0091 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18992 | hp2 | a0005 | c0003 | t0001 | g0258 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18993 | hp1 | a0020 | c0022 | t0001 | g0289 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18993 | hp2 | a0004 | c0008 | t0002 | g0226 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18995 | hp1 | a0010 | c0010 | t0001 | g0027 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18995 | hp2 | a0009 | c0012 | t0002 | g0319 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18998 | hp1 | a0003 | c0002 | t0001 | g0299 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18998 | hp2 | a0004 | c0008 | t0002 | g0225 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18999 | hp1 | a0007 | c0006 | t0001 | g0117 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18999 | hp2 | a0004 | c0008 | t0002 | g0229 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19000 | hp1 | a0006 | c0004 | t0002 | g0242 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19000 | hp2 | a0004 | c0008 | t0001 | g0173 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19002 | hp1 | a0006 | c0044 | t0014 | g0172 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19002 | hp2 | a0012 | c0013 | t0001 | g0140 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19004 | hp1 | a0005 | c0057 | t0001 | g0177 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19004 | hp2 | a0014 | c0030 | t0001 | g0029 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19005 | hp1 | a0006 | c0004 | t0001 | g0248 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19005 | hp2 | a0055 | c0049 | t0002 | g0262 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19006 | hp1 | a0011 | c0011 | t0001 | g0184 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19006 | hp2 | a0008 | c0007 | t0002 | g0137 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19007 | hp1 | a0003 | c0002 | t0001 | g0302 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19007 | hp2 | a0005 | c0003 | t0001 | g0254 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19009 | hp1 | a0004 | c0008 | t0002 | g0327 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19009 | hp2 | a0012 | c0013 | t0001 | g0155 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19010 | hp1 | a0005 | c0003 | t0001 | g0203 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19010 | hp2 | a0008 | c0040 | t0003 | g0138 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19030 | hp1 | a0002 | c0009 | t0001 | g0043 | AFR | LWK | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19030 | hp2 | a0001 | c0082 | t0008 | g0131 | AFR | LWK | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19043 | hp1 | a0013 | c0014 | t0001 | g0066 | AFR | LWK | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19043 | hp2 | a0007 | c0006 | t0001 | g0369 | AFR | LWK | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19054 | hp1 | a0012 | c0013 | t0001 | g0136 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19054 | hp2 | a0005 | c0003 | t0001 | g0255 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19055 | hp1 | a0003 | c0002 | t0001 | g0270 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19055 | hp2 | a0008 | c0007 | t0002 | g0133 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19056 | hp1 | a0003 | c0002 | t0001 | g0287 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19056 | hp2 | a0004 | c0008 | t0002 | g0328 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19057 | hp1 | a0007 | c0006 | t0001 | g0118 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19057 | hp2 | a0003 | c0002 | t0001 | g0321 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19060 | hp1 | a0007 | c0006 | t0001 | g0120 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19060 | hp2 | a0017 | c0025 | t0001 | g0093 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19063 | hp1 | a0018 | c0018 | t0001 | g0318 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19063 | hp2 | a0016 | c0020 | t0001 | g0147 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19065 | hp1 | a0006 | c0004 | t0001 | g0201 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19065 | hp2 | a0003 | c0002 | t0001 | g0296 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19066 | hp1 | a0004 | c0008 | t0002 | g0224 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19066 | hp2 | a0003 | c0015 | t0003 | g0267 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19068 | hp1 | a0016 | c0020 | t0001 | g0078 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19068 | hp2 | a0006 | c0004 | t0001 | g0185 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19074 | hp1 | a0009 | c0012 | t0002 | g0304 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19074 | hp2 | a0003 | c0015 | t0001 | g0264 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19076 | hp2 | a0017 | c0025 | t0001 | g0017 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19079 | hp1 | a0003 | c0002 | t0001 | g0313 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19079 | hp2 | a0049 | c0053 | t0001 | g0231 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19081 | hp1 | a0005 | c0003 | t0001 | g0199 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19081 | hp2 | a0012 | c0013 | t0001 | g0146 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19087 | hp1 | a0003 | c0002 | t0001 | g0291 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19087 | hp2 | a0008 | c0007 | t0002 | g0139 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19088 | hp1 | a0009 | c0012 | t0002 | g0288 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19088 | hp2 | a0004 | c0008 | t0001 | g0329 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19091 | hp1 | a0004 | c0008 | t0002 | g0239 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19091 | hp2 | a0003 | c0002 | t0001 | g0266 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19240 | hp1 | a0037 | c0080 | t0001 | g0165 | AFR | YRI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA19240 | hp2 | a0002 | c0009 | t0001 | g0042 | AFR | YRI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA20129 | hp1 | a0014 | c0024 | t0001 | g0162 | AFR | ASW | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA20129 | hp2 | a0004 | c0019 | t0001 | g0200 | AFR | ASW | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA20752 | hp1 | a0052 | c0064 | t0001 | g0196 | EUR | TSI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0163 | EUR | TSI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0323 | EUR | TSI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA20805 | hp2 | a0002 | c0009 | t0003 | g0362 | EUR | TSI | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG01123 | hp2 | a0006 | c0004 | t0001 | g0213 | AMR | CLM | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02109 | hp1 | a0039 | c0078 | t0003 | g0005 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02109 | hp2 | a0027 | c0034 | t0003 | g0166 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02486 | hp1 | a0019 | c0023 | t0001 | g0241 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02486 | hp2 | a0001 | c0016 | t0001 | g0040 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02559 | hp1 | a0013 | c0014 | t0001 | g0068 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG02559 | hp2 | a0002 | c0037 | t0003 | g0360 | AFR | ACB | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03471 | hp1 | a0002 | c0009 | t0001 | g0039 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG03471 | hp2 | a0001 | c0031 | t0005 | g0330 | AFR | MSL | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG06807 | hp1 | a0002 | c0009 | t0001 | g0037 | AFR | USA | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| HG06807 | hp2 | a0003 | c0002 | t0001 | g0305 | AFR | USA | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18955 | hp1 | a0017 | c0025 | t0001 | g0098 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA18955 | hp2 | a0003 | c0015 | t0001 | g0312 | EAS | JPT | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA20300 | hp1 | a0002 | c0005 | t0001 | g0129 | AFR | USA | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA20300 | hp2 | a0010 | c0010 | t0001 | g0148 | AFR | USA | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| NA21309 | hp2 | a0013 | c0014 | t0001 | g0067 | AFR | LWK | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| homoSapiens_chm13v2 | hp1 | a0004 | c0055 | t0001 | g0204 | REF | REF | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| homoSapiens_grch38 | hp1 | a0004 | c0032 | t0002 | g0235 | REF | REF | TNN_chr1_175062833_175153075 | TNN | chr1 | 175062833 | 175153075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:175077421
|
G | T | 2 | a0029a0030 | 2 | HG02965.hp1 HG03041.hp2 |
start_lost | HIGH | c.3G>T | p.Met1? | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 141/5042 | 3/3900 | 1/1299 | chr1 | 175077421 | ||
| chr1:175077476
|
C | G | 1 | a0058 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.58C>G | p.Leu20Val | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 196/5042 | 58/3900 | 20/1299 | chr1 | 175077476 | ||
| chr1:175077653
|
A | G | 30 | a0001a0002a0007others(27): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
missense_variant | MODERATE | c.235A>G | p.Arg79Gly | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 373/5042 | 235/3900 | 79/1299 | chr1 | 175077653 | ||
| chr1:175077690
|
G | A | 2 | a0013a0031 | 9 | HG01358.hp1 HG01891.hp2 HG01943.hp1 others(6): Show |
missense_variant | MODERATE | c.272G>A | p.Arg91His | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 410/5042 | 272/3900 | 91/1299 | chr1 | 175077690 | ||
| chr1:175077699
|
C | T | 1 | a0026 | 2 | HG00738.hp1 HG01993.hp1 |
missense_variant | MODERATE | c.281C>T | p.Thr94Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 419/5042 | 281/3900 | 94/1299 | chr1 | 175077699 | ||
| chr1:175077784
|
G | A | 1 | a0047 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.366G>A | p.Met122Ile | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 504/5042 | 366/3900 | 122/1299 | chr1 | 175077784 | ||
| chr1:175077806
|
C | T | 1 | a0032 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.388C>T | p.Arg130Cys | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 526/5042 | 388/3900 | 130/1299 | chr1 | 175077806 | ||
| chr1:175079461
|
C | T | 1 | a0029 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.538C>T | p.Arg180Cys | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/19 | 676/5042 | 538/3900 | 180/1299 | chr1 | 175079461 | ||
| chr1:175079570
|
T | A | 1 | a0048 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.647T>A | p.Val216Glu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/19 | 785/5042 | 647/3900 | 216/1299 | chr1 | 175079570 | ||
| chr1:175080243
|
G | A | 8 | a0003a0009a0018others(5): Show | 61 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(58): Show |
missense_variant | MODERATE | c.865G>A | p.Asp289Asn | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/19 | 1003/5042 | 865/3900 | 289/1299 | chr1 | 175080243 | ||
| chr1:175080345
|
C | T | 1 | a0054 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.967C>T | p.Pro323Ser | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/19 | 1105/5042 | 967/3900 | 323/1299 | chr1 | 175080345 | ||
| chr1:175080367
|
C | A | 1 | a0049 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.989C>A | p.Thr330Asn | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/19 | 1127/5042 | 989/3900 | 330/1299 | chr1 | 175080367 | ||
| chr1:175080386
|
T | A | 1 | a0023 | 2 | HG02723.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.1008T>A | p.Asn336Lys | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/19 | 1146/5042 | 1008/3900 | 336/1299 | chr1 | 175080386 | ||
| chr1:175083806
|
G | A | 1 | a0023 | 2 | HG02723.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.1105G>A | p.Val369Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/19 | 1243/5042 | 1105/3900 | 369/1299 | chr1 | 175083806 | ||
| chr1:175094242
|
A | G | 1 | a0046 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.1577A>G | p.Asn526Ser | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/19 | 1715/5042 | 1577/3900 | 526/1299 | chr1 | 175094242 | ||
| chr1:175097558
|
TGGTGGGG others(905): Show |
T | 1 | a0054 | 1 | HG01261.hp1 | conservative_inframe_deletion | MODERATE | c.1755_2018del | p.Thr585_Ser672del | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/19 | 1893/5042 | 1755/3900 | 585/1299 | INFO_REALIGN_3_PRIME | chr1 | 175097558 | |
| chr1:175098538
|
G | T | 1 | a0021 | 3 | HG03688.hp1 HG03927.hp1 HG04184.hp1 |
missense_variant | MODERATE | c.2062G>T | p.Val688Leu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/19 | 2200/5042 | 2062/3900 | 688/1299 | chr1 | 175098538 | ||
| chr1:175117080
|
C | T | 4 | a0033a0034a0035others(1): Show | 4 | HG02622.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
missense_variant | MODERATE | c.2261C>T | p.Pro754Leu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/19 | 2399/5042 | 2261/3900 | 754/1299 | chr1 | 175117080 | ||
| chr1:175118593
|
T | C | 19 | a0001a0002a0007others(16): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
missense_variant | MODERATE | c.2419T>C | p.Trp807Arg | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/19 | 2557/5042 | 2419/3900 | 807/1299 | chr1 | 175118593 | ||
| chr1:175118674
|
G | A | 1 | a0040 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.2500G>A | p.Ala834Thr | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/19 | 2638/5042 | 2500/3900 | 834/1299 | chr1 | 175118674 | ||
| chr1:175118710
|
G | A | 2 | a0029a0030 | 2 | HG02965.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.2536G>A | p.Glu846Lys | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/19 | 2674/5042 | 2536/3900 | 846/1299 | chr1 | 175118710 | ||
| chr1:175118749
|
A | G | 17 | a0003a0009a0010others(14): Show | 88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
missense_variant | MODERATE | c.2575A>G | p.Met859Val | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/19 | 2713/5042 | 2575/3900 | 859/1299 | chr1 | 175118749 | ||
| chr1:175123495
|
A | C | 1 | a0052 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.2746A>C | p.Met916Leu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/19 | 2884/5042 | 2746/3900 | 916/1299 | chr1 | 175123495 | ||
| chr1:175123538
|
C | T | 34 | a0001a0003a0006others(31): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
missense_variant | MODERATE | c.2789C>T | p.Pro930Leu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/19 | 2927/5042 | 2789/3900 | 930/1299 | chr1 | 175123538 | ||
| chr1:175123571
|
C | T | 13 | a0001a0011a0013others(10): Show | 95 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(92): Show |
missense_variant | MODERATE | c.2822C>T | p.Thr941Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/19 | 2960/5042 | 2822/3900 | 941/1299 | chr1 | 175123571 | ||
| chr1:175123606
|
G | A | 1 | a0044 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.2857G>A | p.Val953Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/19 | 2995/5042 | 2857/3900 | 953/1299 | chr1 | 175123606 | ||
| chr1:175126994
|
C | T | 1 | a0041 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.2954C>T | p.Thr985Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/19 | 3092/5042 | 2954/3900 | 985/1299 | chr1 | 175126994 | ||
| chr1:175128129
|
G | A | 1 | a0038 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.3143G>A | p.Arg1048His | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/19 | 3281/5042 | 3143/3900 | 1048/1299 | chr1 | 175128129 | ||
| chr1:175128132
|
G | A | 1 | a0040 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.3146G>A | p.Arg1049Gln | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/19 | 3284/5042 | 3146/3900 | 1049/1299 | chr1 | 175128132 | ||
| chr1:175128727
|
C | T | 2 | a0036a0051 | 2 | HG02622.hp2 HG03225.hp1 |
missense_variant | MODERATE | c.3311C>T | p.Thr1104Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/19 | 3449/5042 | 3311/3900 | 1104/1299 | chr1 | 175128727 | ||
| chr1:175135858
|
G | A | 1 | a0037 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.3344G>A | p.Arg1115Gln | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/19 | 3482/5042 | 3344/3900 | 1115/1299 | chr1 | 175135858 | ||
| chr1:175135902
|
G | A | 2 | a0023a0024 | 4 | HG02451.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
missense_variant | MODERATE | c.3388G>A | p.Val1130Met | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/19 | 3526/5042 | 3388/3900 | 1130/1299 | chr1 | 175135902 | ||
| chr1:175135919
|
C | A | 1 | a0035 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.3405C>A | p.Asp1135Glu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/19 | 3543/5042 | 3405/3900 | 1135/1299 | chr1 | 175135919 | ||
| chr1:175136860
|
C | T | 10 | a0005a0014a0016others(7): Show | 50 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(47): Show |
missense_variant | MODERATE | c.3467C>T | p.Ala1156Val | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/19 | 3605/5042 | 3467/3900 | 1156/1299 | chr1 | 175136860 | ||
| chr1:175136950
|
G | A | 1 | a0039 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.3557G>A | p.Arg1186Gln | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/19 | 3695/5042 | 3557/3900 | 1186/1299 | chr1 | 175136950 | ||
| chr1:175146986
|
T | C | 1 | a0057 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.3815T>C | p.Leu1272Ser | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 3953/5042 | 3815/3900 | 1272/1299 | chr1 | 175146986 | ||
| chr1:175147034
|
A | G | 1 | a0056 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.3863A>G | p.Lys1288Arg | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 4001/5042 | 3863/3900 | 1288/1299 | chr1 | 175147034 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:175077643
|
G | A | 1 | a0006c0044 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.225G>A | p.Leu75Leu | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/19 | 363/5042 | 225/3900 | 75/1299 | chr1 | 175077643 | ||
| chr1:175079349
|
C | T | 1 | a0015c0092 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.426C>T | p.Cys142Cys | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/19 | 564/5042 | 426/3900 | 142/1299 | chr1 | 175079349 | ||
| chr1:175079457
|
C | T | 1 | a0023c0043 | 2 | HG02723.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.534C>T | p.His178His | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/19 | 672/5042 | 534/3900 | 178/1299 | chr1 | 175079457 | ||
| chr1:175079598
|
G | A | 1 | a0001c0036 | 2 | HG01106.hp2 HG03654.hp2 |
synonymous_variant | LOW | c.675G>A | p.Ser225Ser | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/19 | 813/5042 | 675/3900 | 225/1299 | chr1 | 175079598 | ||
| chr1:175080269
|
C | A | 9 | a0001c0016a0001c0028a0002c0009others(6): Show | 32 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(29): Show |
synonymous_variant | LOW | c.891C>A | p.Pro297Pro | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/19 | 1029/5042 | 891/3900 | 297/1299 | chr1 | 175080269 | ||
| chr1:175083760
|
G | T | 1 | a0023c0043 | 2 | HG02723.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.1059G>T | p.Val353Val | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/19 | 1197/5042 | 1059/3900 | 353/1299 | chr1 | 175083760 | ||
| chr1:175085412
|
C | T | 49 | a0001c0001a0001c0016a0001c0028others(46): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
synonymous_variant | LOW | c.1242C>T | p.His414His | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/19 | 1380/5042 | 1242/3900 | 414/1299 | chr1 | 175085412 | ||
| chr1:175097583
|
T | C | 1 | a0050c0054 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1755T>C | p.Thr585Thr | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/19 | 1893/5042 | 1755/3900 | 585/1299 | chr1 | 175097583 | ||
| chr1:175097622
|
G | A | 2 | a0003c0047a0010c0076 | 2 | NA18971.hp2 NA18981.hp2 |
synonymous_variant | LOW | c.1794G>A | p.Val598Val | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/19 | 1932/5042 | 1794/3900 | 598/1299 | chr1 | 175097622 | ||
| chr1:175098444
|
T | C | 1 | a0004c0055 | 1 | homoSapiens_chm13v2.hp1 | synonymous_variant | LOW | c.1968T>C | p.Ser656Ser | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/19 | 2106/5042 | 1968/3900 | 656/1299 | chr1 | 175098444 | ||
| chr1:175098513
|
A | G | 3 | a0001c0042a0002c0026a0036c0090 | 7 | HG01070.hp2 HG01071.hp1 HG02922.hp1 others(4): Show |
synonymous_variant | LOW | c.2037A>G | p.Arg679Arg | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/19 | 2175/5042 | 2037/3900 | 679/1299 | chr1 | 175098513 | ||
| chr1:175098576
|
C | T | 1 | a0001c0089 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.2100C>T | p.Ala700Ala | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/19 | 2238/5042 | 2100/3900 | 700/1299 | chr1 | 175098576 | ||
| chr1:175117081
|
G | A | 1 | a0004c0056 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.2262G>A | p.Pro754Pro | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/19 | 2400/5042 | 2262/3900 | 754/1299 | chr1 | 175117081 | ||
| chr1:175117126
|
G | A | 1 | a0005c0057 | 1 | NA19004.hp1 | synonymous_variant | LOW | c.2307G>A | p.Pro769Pro | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/19 | 2445/5042 | 2307/3900 | 769/1299 | chr1 | 175117126 | ||
| chr1:175118634
|
G | A | 1 | a0003c0048 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.2460G>A | p.Val820Val | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/19 | 2598/5042 | 2460/3900 | 820/1299 | chr1 | 175118634 | ||
| chr1:175118748
|
C | T | 24 | a0003c0002a0003c0015a0003c0047others(21): Show | 88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
synonymous_variant | LOW | c.2574C>T | p.Gly858Gly | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/19 | 2712/5042 | 2574/3900 | 858/1299 | chr1 | 175118748 | ||
| chr1:175123440
|
G | A | 1 | a0043c0086 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.2691G>A | p.Thr897Thr | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/19 | 2829/5042 | 2691/3900 | 897/1299 | chr1 | 175123440 | ||
| chr1:175123647
|
C | T | 1 | a0022c0060 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.2898C>T | p.Asp966Asp | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/19 | 3036/5042 | 2898/3900 | 966/1299 | chr1 | 175123647 | ||
| chr1:175127022
|
G | A | 4 | a0022c0058a0022c0060a0037c0080others(1): Show | 4 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(1): Show |
synonymous_variant | LOW | c.2982G>A | p.Thr994Thr | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/19 | 3120/5042 | 2982/3900 | 994/1299 | chr1 | 175127022 | ||
| chr1:175127043
|
C | T | 2 | a0001c0028a0001c0083 | 4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.3003C>T | p.His1001His | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/19 | 3141/5042 | 3003/3900 | 1001/1299 | chr1 | 175127043 | ||
| chr1:175128686
|
C | T | 4 | a0023c0043a0024c0039a0036c0090others(1): Show | 6 | HG02451.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
synonymous_variant | LOW | c.3270C>T | p.Gly1090Gly | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/19 | 3408/5042 | 3270/3900 | 1090/1299 | chr1 | 175128686 | ||
| chr1:175128728
|
G | A | 18 | a0001c0031a0003c0015a0004c0019others(15): Show | 68 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(65): Show |
synonymous_variant | LOW | c.3312G>A | p.Thr1104Thr | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/19 | 3450/5042 | 3312/3900 | 1104/1299 | chr1 | 175128728 | ||
| chr1:175128731
|
C | T | 2 | a0002c0037a0009c0050 | 3 | HG02559.hp2 HG02809.hp2 NA18970.hp1 |
synonymous_variant | LOW | c.3315C>T | p.Asp1105Asp | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/19 | 3453/5042 | 3315/3900 | 1105/1299 | chr1 | 175128731 | ||
| chr1:175136849
|
C | T | 1 | a0001c0082 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.3456C>T | p.Thr1152Thr | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/19 | 3594/5042 | 3456/3900 | 1152/1299 | chr1 | 175136849 | ||
| chr1:175136861
|
G | A | 1 | a0007c0081 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.3468G>A | p.Ala1156Ala | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/19 | 3606/5042 | 3468/3900 | 1156/1299 | chr1 | 175136861 | ||
| chr1:175136864
|
G | T | 1 | a0002c0079 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.3471G>T | p.Arg1157Arg | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/19 | 3609/5042 | 3471/3900 | 1157/1299 | chr1 | 175136864 | ||
| chr1:175144442
|
T | C | 93 | a0001c0001a0001c0016a0001c0028others(90): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
synonymous_variant | LOW | c.3651T>C | p.Asn1217Asn | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/19 | 3789/5042 | 3651/3900 | 1217/1299 | chr1 | 175144442 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:175067873
|
C | T | 1 | a0002c0005t0016 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-98C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/19 | 9546 | chr1 | 175067873 | |||||
| chr1:175067903
|
C | T | 7 | a0002c0005t0004a0007c0006t0004a0007c0006t0015others(4): Show | 8 | HG01891.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-68C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/19 | 9516 | chr1 | 175067903 | |||||
| chr1:175147116
|
C | G | 107 | a0001c0001t0001a0001c0016t0001a0001c0016t0008others(104): Show | 319 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*45C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 45 | chr1 | 175147116 | |||||
| chr1:175147141
|
T | A | 18 | a0002c0005t0003a0002c0009t0003a0002c0026t0003others(15): Show | 35 | HG01109.hp2 HG01192.hp1 HG01433.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*70T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 70 | chr1 | 175147141 | |||||
| chr1:175147147
|
C | G | 2 | a0001c0028t0007a0002c0005t0007 | 3 | HG02717.hp2 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*76C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 76 | chr1 | 175147147 | |||||
| chr1:175147382
|
C | A | 3 | a0001c0031t0005a0036c0090t0005a0051c0066t0010 | 5 | HG01884.hp1 HG02622.hp2 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*311C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 311 | chr1 | 175147382 | |||||
| chr1:175147400
|
G | C | 1 | a0007c0038t0011 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*329G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 329 | chr1 | 175147400 | |||||
| chr1:175147496
|
C | T | 1 | a0006c0044t0014 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*425C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 425 | chr1 | 175147496 | |||||
| chr1:175147521
|
T | C | 1 | a0003c0002t0012 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*450T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 450 | chr1 | 175147521 | |||||
| chr1:175147676
|
G | A | 1 | a0007c0006t0015 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*605G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 605 | chr1 | 175147676 | |||||
| chr1:175147781
|
A | G | 2 | a0001c0016t0008a0001c0082t0008 | 2 | HG02970.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*710A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 710 | chr1 | 175147781 | |||||
| chr1:175147799
|
T | C | 1 | a0051c0066t0010 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*728T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 728 | chr1 | 175147799 | |||||
| chr1:175147869
|
C | T | 1 | a0002c0009t0013 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*798C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 798 | chr1 | 175147869 | |||||
| chr1:175147936
|
G | A | 3 | a0022c0058t0006a0022c0060t0006a0031c0068t0006 | 3 | HG01943.hp1 HG02145.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*865G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 19/19 | 865 | chr1 | 175147936 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:175068081
|
G | C | 1 | a0009c0021t0001g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-36+146G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068081 | ||||||
| chr1:175068086
|
A | G | 17 | a0001c0016t0001g0355a0001c0016t0001g0356a0001c0016t0001g0358others(14): Show | 17 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36+151A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068086 | ||||||
| chr1:175068157
|
G | T | 1 | a0011c0011t0001g0354 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-36+222G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068157 | ||||||
| chr1:175068538
|
C | T | 1 | a0004c0019t0001g0353 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-36+603C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068538 | ||||||
| chr1:175068559
|
C | T | 23 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0001g0333others(20): Show | 23 | HG00099.hp2 HG01106.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.-36+624C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068559 | ||||||
| chr1:175068634
|
T | C | 206 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(203): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-36+699T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068634 | ||||||
| chr1:175068662
|
T | G | 1 | a0001c0016t0001g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-36+727T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068662 | ||||||
| chr1:175068856
|
C | T | 3 | a0027c0034t0003g0166a0027c0034t0003g0168a0051c0066t0010g0167 | 3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-36+921C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175068856 | ||||||
| chr1:175069162
|
A | G | 3 | a0004c0008t0001g0329a0004c0008t0002g0327a0004c0008t0002g0328 | 3 | NA19009.hp1 NA19056.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-36+1227A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069162 | ||||||
| chr1:175069212
|
A | G | 274 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(271): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-36+1277A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069212 | ||||||
| chr1:175069222
|
C | T | 2 | a0001c0001t0001g0164a0037c0080t0001g0165 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-36+1287C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069222 | ||||||
| chr1:175069235
|
G | A | 93 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(90): Show | 93 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(90): Show |
intron_variant | MODIFIER | c.-36+1300G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069235 | ||||||
| chr1:175069323
|
T | C | 7 | a0003c0002t0001g0266a0003c0015t0001g0264a0003c0015t0003g0261others(4): Show | 7 | NA18977.hp1 NA18981.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.-36+1388T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069323 | ||||||
| chr1:175069586
|
T | C | 3 | a0007c0006t0001g0006a0007c0006t0001g0007a0039c0078t0003g0005 | 3 | HG02109.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-36+1651T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069586 | ||||||
| chr1:175069699
|
A | G | 206 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(203): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-36+1764A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069699 | ||||||
| chr1:175069735
|
A | G | 1 | a0009c0012t0002g0326 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-36+1800A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069735 | ||||||
| chr1:175069871
|
A | C | 1 | a0001c0001t0002g0163 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-36+1936A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069871 | ||||||
| chr1:175069878
|
C | A | 1 | a0013c0014t0001g0056 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-36+1943C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069878 | ||||||
| chr1:175069919
|
A | T | 1 | a0003c0002t0001g0325 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-36+1984A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175069919 | ||||||
| chr1:175070161
|
A | G | 5 | a0001c0074t0001g0052a0002c0029t0001g0055a0002c0029t0003g0053others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+2226A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175070161 | ||||||
| chr1:175070464
|
C | T | 1 | a0014c0030t0001g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-36+2529C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175070464 | ||||||
| chr1:175070467
|
T | C | 50 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(47): Show | 50 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.-36+2532T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175070467 | ||||||
| chr1:175070627
|
C | T | 2 | a0014c0024t0001g0161a0014c0024t0001g0162 | 2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-36+2692C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175070627 | ||||||
| chr1:175070890
|
G | A | 1 | a0053c0065t0001g0268 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-36+2955G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175070890 | ||||||
| chr1:175070912
|
C | T | 206 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(203): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-36+2977C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175070912 | ||||||
| chr1:175071729
|
G | T | 3 | a0007c0006t0001g0369a0007c0006t0001g0371a0014c0024t0001g0370 | 3 | HG02886.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-36+3794G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175071729 | ||||||
| chr1:175071771
|
T | C | 1 | a0001c0001t0002g0163 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-36+3836T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175071771 | ||||||
| chr1:175071805
|
G | A | 3 | a0027c0034t0003g0166a0027c0034t0003g0168a0051c0066t0010g0167 | 3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-36+3870G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175071805 | ||||||
| chr1:175072016
|
C | A | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-36+4081C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072016 | ||||||
| chr1:175072030
|
G | T | 5 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0031t0005g0156others(2): Show | 5 | HG01192.hp2 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+4095G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072030 | ||||||
| chr1:175072250
|
C | A | 1 | a0038c0069t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-36+4315C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072250 | ||||||
| chr1:175072391
|
G | A | 7 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0001g0333others(4): Show | 7 | HG01884.hp2 HG02145.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+4456G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072391 | ||||||
| chr1:175072413
|
A | G | 110 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(107): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-36+4478A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072413 | ||||||
| chr1:175072437
|
A | T | 40 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(37): Show | 40 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.-36+4502A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072437 | ||||||
| chr1:175072558
|
G | C | 1 | a0001c0031t0005g0330 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-36+4623G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072558 | ||||||
| chr1:175072682
|
T | C | 1 | a0005c0003t0001g0169 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-35-4702T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072682 | ||||||
| chr1:175072841
|
G | T | 208 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-4543G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072841 | ||||||
| chr1:175072910
|
T | C | 93 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(90): Show | 93 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(90): Show |
intron_variant | MODIFIER | c.-35-4474T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072910 | ||||||
| chr1:175072917
|
A | G | 1 | a0007c0038t0011g0368 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-35-4467A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175072917 | ||||||
| chr1:175072926
|
C | CT | 48 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(45): Show | 48 | HG00438.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.-35-4434dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175072926 | |||||
| chr1:175072926
|
CT | C | 138 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-35-4434delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175072926 | |||||
| chr1:175072926
|
CTTTTTTT others(4): Show |
C | 3 | a0007c0006t0001g0369a0007c0006t0001g0371a0014c0024t0001g0370 | 3 | HG02886.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-35-4444_-35-4434d others(13): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175072926 | |||||
| chr1:175073020
|
C | G | 208 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-4364C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073020 | ||||||
| chr1:175073069
|
C | T | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-35-4315C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073069 | ||||||
| chr1:175073172
|
T | C | 208 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-4212T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073172 | ||||||
| chr1:175073309
|
C | T | 208 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-4075C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073309 | ||||||
| chr1:175073318
|
T | G | 1 | a0020c0022t0001g0269 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-35-4066T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073318 | ||||||
| chr1:175073577
|
C | T | 1 | a0007c0006t0001g0153 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-35-3807C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073577 | ||||||
| chr1:175073690
|
C | T | 115 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(112): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.-35-3694C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073690 | ||||||
| chr1:175073876
|
C | T | 2 | a0014c0024t0001g0161a0014c0024t0001g0162 | 2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-35-3508C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175073876 | ||||||
| chr1:175073924
|
A | AGCTCGGG others(14): Show |
11 | a0001c0016t0001g0040a0002c0009t0001g0036a0002c0009t0001g0037others(8): Show | 11 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-35-3459_-35-3439d others(23): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175073924 | |||||
| chr1:175074023
|
T | C | 1 | a0015c0017t0001g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-35-3361T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074023 | ||||||
| chr1:175074062
|
G | A | 208 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-3322G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074062 | ||||||
| chr1:175074107
|
A | G | 208 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-3277A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074107 | ||||||
| chr1:175074273
|
A | G | 208 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-3111A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074273 | ||||||
| chr1:175074421
|
A | T | 3 | a0001c0001t0001g0125a0010c0076t0001g0152a0016c0020t0001g0126 | 3 | NA18981.hp2 NA18982.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-35-2963A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074421 | ||||||
| chr1:175074484
|
G | GA | 63 | a0003c0002t0001g0266a0003c0002t0001g0278a0003c0002t0001g0279others(60): Show | 64 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-35-2875dupA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175074484 | |||||
| chr1:175074484
|
G | GAA | 6 | a0003c0002t0001g0270a0003c0002t0001g0313a0003c0002t0001g0315others(3): Show | 6 | NA18950.hp1 NA18955.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35-2876_-35-2875d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175074484 | |||||
| chr1:175074484
|
GAAAAAAA others(2): Show |
G | 47 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(44): Show | 47 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.-35-2883_-35-2875d others(11): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175074484 | |||||
| chr1:175074484
|
GAAAAAAA others(3): Show |
G | 160 | a0001c0001t0001g0031a0001c0001t0001g0070a0001c0001t0001g0074others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-35-2884_-35-2875d others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175074484 | |||||
| chr1:175074484
|
GAAAAAAA others(4): Show |
G | 1 | a0015c0092t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-35-2885_-35-2875d others(13): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175074484 | |||||
| chr1:175074543
|
G | T | 5 | a0004c0008t0002g0239a0004c0019t0002g0237a0006c0004t0002g0242others(2): Show | 5 | HG00408.hp1 HG02040.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-2841G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074543 | ||||||
| chr1:175074754
|
T | C | 2 | a0029c0096t0001g0308a0030c0095t0003g0307 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-35-2630T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074754 | ||||||
| chr1:175074819
|
T | C | 11 | a0004c0008t0003g0246a0004c0008t0003g0247a0004c0019t0001g0353others(8): Show | 11 | HG01069.hp2 HG01071.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35-2565T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074819 | ||||||
| chr1:175074831
|
C | T | 9 | a0001c0074t0001g0052a0002c0029t0001g0055a0002c0029t0003g0053others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-35-2553C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074831 | ||||||
| chr1:175074929
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0151 | 2 | HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-35-2455C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074929 | ||||||
| chr1:175074943
|
C | G | 3 | a0027c0034t0003g0166a0027c0034t0003g0168a0051c0066t0010g0167 | 3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-35-2441C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175074943 | ||||||
| chr1:175075321
|
C | T | 3 | a0033c0072t0004g0013a0034c0070t0004g0014a0035c0071t0004g0015 | 3 | HG02622.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-35-2063C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075321 | ||||||
| chr1:175075418
|
T | C | 112 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.-35-1966T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075418 | ||||||
| chr1:175075546
|
A | G | 66 | a0003c0002t0001g0266a0003c0002t0001g0270a0003c0002t0001g0278others(63): Show | 67 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-35-1838A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075546 | ||||||
| chr1:175075546
|
A | T | 208 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-1838A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075546 | ||||||
| chr1:175075664
|
T | C | 93 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(90): Show | 93 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(90): Show |
intron_variant | MODIFIER | c.-35-1720T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075664 | ||||||
| chr1:175075694
|
T | C | 93 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(90): Show | 93 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(90): Show |
intron_variant | MODIFIER | c.-35-1690T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075694 | ||||||
| chr1:175075870
|
A | G | 1 | a0048c0046t0001g0306 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-35-1514A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075870 | ||||||
| chr1:175075878
|
G | A | 93 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(90): Show | 93 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(90): Show |
intron_variant | MODIFIER | c.-35-1506G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175075878 | ||||||
| chr1:175076080
|
A | T | 91 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(88): Show | 91 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(88): Show |
intron_variant | MODIFIER | c.-35-1304A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076080 | ||||||
| chr1:175076158
|
A | T | 3 | a0027c0034t0003g0166a0027c0034t0003g0168a0051c0066t0010g0167 | 3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-35-1226A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076158 | ||||||
| chr1:175076198
|
A | T | 44 | a0001c0001t0001g0164a0001c0016t0001g0040a0001c0016t0001g0355others(41): Show | 44 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.-35-1186A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076198 | ||||||
| chr1:175076223
|
G | A | 1 | a0015c0092t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-35-1161G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076223 | ||||||
| chr1:175076350
|
C | A | 208 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-1034C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076350 | ||||||
| chr1:175076632
|
T | G | 208 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-35-752T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076632 | ||||||
| chr1:175076704
|
G | A | 12 | a0001c0001t0001g0164a0002c0005t0004g0008a0007c0006t0001g0369others(9): Show | 12 | HG01891.hp1 HG02451.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-35-680G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076704 | ||||||
| chr1:175076749
|
C | G | 31 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0123others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-35-635C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076749 | ||||||
| chr1:175076766
|
G | C | 115 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(112): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.-35-618G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076766 | ||||||
| chr1:175076936
|
T | C | 3 | a0027c0034t0003g0166a0027c0034t0003g0168a0051c0066t0010g0167 | 3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-35-448T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175076936 | ||||||
| chr1:175077318
|
T | TAA | 32 | a0001c0016t0001g0040a0001c0016t0001g0355a0001c0016t0001g0356others(29): Show | 32 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.-35-58_-35-57dupAA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 175077318 | |||||
| chr1:175077341
|
A | G | 10 | a0001c0001t0001g0164a0002c0005t0004g0008a0007c0006t0001g0369others(7): Show | 10 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35-43A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175077341 | ||||||
| chr1:175077352
|
G | A | 205 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-35-32G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 1/18 | chr1 | 175077352 | ||||||
| chr1:175077971
|
T | G | 5 | a0001c0001t0001g0164a0007c0006t0001g0369a0007c0006t0001g0371others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.409+144T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175077971 | ||||||
| chr1:175077983
|
A | G | 5 | a0001c0001t0001g0164a0007c0006t0001g0369a0007c0006t0001g0371others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.409+156A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175077983 | ||||||
| chr1:175078104
|
C | T | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.409+277C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078104 | ||||||
| chr1:175078164
|
T | C | 1 | a0006c0004t0001g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.409+337T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078164 | ||||||
| chr1:175078220
|
C | T | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.409+393C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078220 | ||||||
| chr1:175078223
|
T | C | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.409+396T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078223 | ||||||
| chr1:175078236
|
A | G | 1 | a0016c0020t0001g0147 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.409+409A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078236 | ||||||
| chr1:175078246
|
T | C | 62 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(59): Show | 62 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.409+419T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078246 | ||||||
| chr1:175078440
|
C | T | 3 | a0033c0072t0004g0013a0034c0070t0004g0014a0035c0071t0004g0015 | 3 | HG02622.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.409+613C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078440 | ||||||
| chr1:175078453
|
G | A | 3 | a0009c0012t0003g0273a0009c0021t0001g0271a0009c0021t0001g0272 | 3 | HG01109.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.409+626G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078453 | ||||||
| chr1:175078581
|
C | T | 1 | a0036c0090t0005g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.410-752C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078581 | ||||||
| chr1:175078618
|
C | T | 1 | a0002c0029t0001g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.410-715C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078618 | ||||||
| chr1:175078656
|
G | C | 92 | a0004c0008t0001g0173a0004c0008t0001g0228a0004c0008t0001g0329others(89): Show | 92 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.410-677G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078656 | ||||||
| chr1:175078664
|
A | G | 62 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(59): Show | 62 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.410-669A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078664 | ||||||
| chr1:175078757
|
G | A | 1 | a0005c0003t0001g0176 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.410-576G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078757 | ||||||
| chr1:175078917
|
T | C | 2 | a0001c0001t0001g0331a0044c0087t0001g0335 | 2 | HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.410-416T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175078917 | ||||||
| chr1:175079008
|
G | T | 208 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.410-325G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175079008 | ||||||
| chr1:175079028
|
G | A | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.410-305G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 2/18 | chr1 | 175079028 | ||||||
| chr1:175079815
|
C | G | 1 | a0012c0013t0001g0101 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.784+108C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/18 | chr1 | 175079815 | ||||||
| chr1:175079873
|
G | T | 5 | a0001c0001t0001g0123a0001c0001t0001g0151a0001c0001t0002g0122others(2): Show | 5 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+166G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/18 | chr1 | 175079873 | ||||||
| chr1:175079880
|
T | C | 1 | a0044c0087t0001g0335 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.784+173T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/18 | chr1 | 175079880 | ||||||
| chr1:175079967
|
A | AGT | 212 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(209): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.785-180_785-179dup others(2): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 175079967 | |||||
| chr1:175079967
|
A | AGTGT | 4 | a0010c0010t0001g0025a0010c0010t0001g0026a0010c0010t0001g0027others(1): Show | 4 | NA18966.hp1 NA18985.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.785-182_785-179dup others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 175079967 | |||||
| chr1:175080448
|
C | T | 1 | a0003c0002t0001g0322 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1048+22C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080448 | ||||||
| chr1:175080460
|
G | C | 1 | a0002c0005t0001g0121 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1048+34G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080460 | ||||||
| chr1:175080499
|
C | T | 2 | a0001c0001t0001g0350a0040c0077t0001g0348 | 2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1048+73C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080499 | ||||||
| chr1:175080731
|
T | G | 1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1048+305T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080731 | ||||||
| chr1:175080752
|
A | C | 1 | a0019c0023t0001g0241 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1048+326A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080752 | ||||||
| chr1:175080755
|
G | A | 4 | a0002c0005t0003g0103a0002c0005t0003g0105a0002c0005t0003g0106others(1): Show | 4 | HG01192.hp1 HG01943.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048+329G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080755 | ||||||
| chr1:175080814
|
C | G | 202 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1048+388C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175080814 | ||||||
| chr1:175081046
|
C | G | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1048+620C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081046 | ||||||
| chr1:175081098
|
C | A | 3 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046 | 3 | HG02896.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1048+672C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081098 | ||||||
| chr1:175081297
|
C | T | 1 | a0050c0054t0001g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1048+871C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081297 | ||||||
| chr1:175081343
|
C | T | 1 | a0031c0068t0006g0100 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1048+917C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081343 | ||||||
| chr1:175081423
|
C | A | 202 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1048+997C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081423 | ||||||
| chr1:175081699
|
G | A | 1 | a0005c0057t0001g0177 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1048+1273G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081699 | ||||||
| chr1:175081733
|
A | G | 1 | a0002c0005t0003g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1048+1307A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081733 | ||||||
| chr1:175081742
|
GACCATAG others(4): Show |
G | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1048+1318_1048+132 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 175081742 | |||||
| chr1:175081747
|
T | C | 6 | a0001c0001t0001g0338a0001c0001t0001g0351a0001c0036t0001g0340others(3): Show | 6 | HG00099.hp2 HG01106.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048+1321T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081747 | ||||||
| chr1:175081766
|
C | G | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1048+1340C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081766 | ||||||
| chr1:175081816
|
G | C | 112 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1048+1390G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081816 | ||||||
| chr1:175081889
|
A | C | 1 | a0002c0005t0001g0121 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1048+1463A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175081889 | ||||||
| chr1:175082215
|
T | G | 3 | a0019c0023t0001g0309a0022c0058t0006g0274a0022c0060t0006g0316 | 3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1049-1535T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175082215 | ||||||
| chr1:175082391
|
T | C | 112 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1049-1359T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175082391 | ||||||
| chr1:175082396
|
G | A | 2 | a0009c0012t0002g0326a0018c0018t0001g0275 | 2 | HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1049-1354G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175082396 | ||||||
| chr1:175082448
|
C | T | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1049-1302C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175082448 | ||||||
| chr1:175082501
|
A | C | 1 | a0002c0005t0003g0106 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1049-1249A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175082501 | ||||||
| chr1:175082707
|
A | G | 274 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(271): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1049-1043A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175082707 | ||||||
| chr1:175082983
|
G | GT | 52 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(49): Show | 52 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1049-754dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 175082983 | |||||
| chr1:175083084
|
T | C | 2 | a0005c0003t0001g0178a0005c0003t0001g0179 | 2 | NA18612.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1049-666T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083084 | ||||||
| chr1:175083254
|
G | A | 200 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1049-496G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083254 | ||||||
| chr1:175083273
|
C | A | 1 | a0005c0003t0001g0180 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1049-477C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083273 | ||||||
| chr1:175083489
|
G | A | 2 | a0005c0003t0001g0181a0006c0004t0001g0182 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1049-261G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083489 | ||||||
| chr1:175083518
|
G | GA | 3 | a0019c0023t0001g0309a0022c0058t0006g0274a0022c0060t0006g0316 | 3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1049-232_1049-231i others(3): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083518 | ||||||
| chr1:175083520
|
G | A | 3 | a0019c0023t0001g0309a0022c0058t0006g0274a0022c0060t0006g0316 | 3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1049-230G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083520 | ||||||
| chr1:175083692
|
G | A | 112 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1049-58G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 4/18 | chr1 | 175083692 | ||||||
| chr1:175083962
|
T | C | 43 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(40): Show | 43 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.1234+27T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175083962 | ||||||
| chr1:175083965
|
A | T | 202 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1234+30A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175083965 | ||||||
| chr1:175084252
|
A | G | 1 | a0008c0007t0002g0099 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1234+317A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084252 | ||||||
| chr1:175084301
|
C | A | 6 | a0007c0006t0001g0006a0007c0006t0001g0007a0027c0034t0003g0166others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234+366C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084301 | ||||||
| chr1:175084438
|
C | T | 1 | a0013c0014t0001g0056 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1234+503C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084438 | ||||||
| chr1:175084484
|
A | T | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1234+549A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084484 | ||||||
| chr1:175084550
|
C | T | 2 | a0001c0001t0001g0351a0002c0005t0002g0342 | 2 | HG01361.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1234+615C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084550 | ||||||
| chr1:175084562
|
T | C | 1 | a0038c0069t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1234+627T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084562 | ||||||
| chr1:175084581
|
C | T | 1 | a0015c0092t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1234+646C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084581 | ||||||
| chr1:175084713
|
T | A | 3 | a0027c0034t0003g0166a0027c0034t0003g0168a0051c0066t0010g0167 | 3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1235-692T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084713 | ||||||
| chr1:175084792
|
G | T | 1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1235-613G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084792 | ||||||
| chr1:175084886
|
A | G | 6 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1235-519A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175084886 | ||||||
| chr1:175085233
|
C | T | 1 | a0005c0003t0001g0232 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1235-172C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175085233 | ||||||
| chr1:175085282
|
A | G | 205 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1235-123A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175085282 | ||||||
| chr1:175085321
|
C | T | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1235-84C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175085321 | ||||||
| chr1:175085353
|
G | C | 5 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1235-52G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 5/18 | chr1 | 175085353 | ||||||
| chr1:175085643
|
G | A | 2 | a0029c0096t0001g0308a0030c0095t0003g0307 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1324+149G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175085643 | ||||||
| chr1:175085644
|
G | A | 11 | a0001c0016t0001g0040a0002c0009t0001g0036a0002c0009t0001g0037others(8): Show | 11 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1324+150G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175085644 | ||||||
| chr1:175085828
|
C | T | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1324+334C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175085828 | ||||||
| chr1:175085874
|
C | CA | 8 | a0001c0042t0001g0097a0002c0005t0003g0149a0007c0006t0001g0006others(5): Show | 8 | HG01358.hp2 HG02895.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324+400dupA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175085874 | |||||
| chr1:175085874
|
C | CAA | 113 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0123others(110): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1324+399_1324+400d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175085874 | |||||
| chr1:175085874
|
C | CAAA | 77 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(74): Show | 77 | HG00099.hp2 HG00438.hp1 HG01074.hp2 others(74): Show |
intron_variant | MODIFIER | c.1324+398_1324+400d others(5): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175085874 | |||||
| chr1:175086086
|
C | A | 200 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1324+592C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086086 | ||||||
| chr1:175086418
|
C | A | 45 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(42): Show | 45 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1324+924C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086418 | ||||||
| chr1:175086420
|
A | G | 1 | a0049c0053t0001g0231 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1324+926A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086420 | ||||||
| chr1:175086512
|
C | T | 112 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1324+1018C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086512 | ||||||
| chr1:175086514
|
T | C | 274 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(271): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1324+1020T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086514 | ||||||
| chr1:175086517
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1324+1023G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086517 | ||||||
| chr1:175086572
|
G | A | 1 | a0014c0030t0001g0016 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1324+1078G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086572 | ||||||
| chr1:175086783
|
T | C | 3 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046 | 3 | HG02896.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1324+1289T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086783 | ||||||
| chr1:175086815
|
T | C | 200 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1324+1321T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175086815 | ||||||
| chr1:175087027
|
C | T | 1 | a0009c0012t0002g0304 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1324+1533C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087027 | ||||||
| chr1:175087029
|
G | C | 202 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1324+1535G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087029 | ||||||
| chr1:175087070
|
A | C | 1 | a0015c0092t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1324+1576A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087070 | ||||||
| chr1:175087078
|
A | C | 1 | a0006c0004t0002g0242 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1324+1584A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087078 | ||||||
| chr1:175087104
|
A | C | 1 | a0050c0054t0001g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1324+1610A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087104 | ||||||
| chr1:175087167
|
C | T | 1 | a0008c0007t0002g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1324+1673C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087167 | ||||||
| chr1:175087215
|
C | A | 200 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1324+1721C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087215 | ||||||
| chr1:175087380
|
G | A | 202 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1324+1886G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087380 | ||||||
| chr1:175087418
|
C | T | 45 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(42): Show | 45 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1324+1924C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087418 | ||||||
| chr1:175087421
|
C | T | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1324+1927C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087421 | ||||||
| chr1:175087733
|
T | A | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1324+2239T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087733 | ||||||
| chr1:175087797
|
A | G | 198 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(195): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1324+2303A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087797 | ||||||
| chr1:175087807
|
C | A | 55 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(52): Show | 55 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.1324+2313C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087807 | ||||||
| chr1:175087852
|
C | T | 2 | a0005c0003t0001g0230a0005c0003t0001g0232 | 2 | HG02132.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1324+2358C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087852 | ||||||
| chr1:175087867
|
C | A | 44 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(41): Show | 44 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.1324+2373C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087867 | ||||||
| chr1:175087882
|
G | A | 32 | a0001c0016t0001g0040a0001c0016t0001g0355a0001c0016t0001g0356others(29): Show | 32 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1324+2388G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087882 | ||||||
| chr1:175087895
|
C | T | 3 | a0002c0029t0001g0055a0002c0029t0003g0053a0002c0029t0003g0054 | 3 | HG02630.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1324+2401C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087895 | ||||||
| chr1:175087896
|
G | A | 1 | a0008c0007t0002g0058 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1324+2402G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087896 | ||||||
| chr1:175087922
|
C | A | 1 | a0006c0004t0002g0242 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1324+2428C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175087922 | ||||||
| chr1:175088056
|
C | A | 3 | a0027c0034t0003g0166a0027c0034t0003g0168a0051c0066t0010g0167 | 3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1324+2562C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088056 | ||||||
| chr1:175088112
|
G | A | 14 | a0001c0016t0001g0355a0001c0016t0001g0356a0001c0016t0001g0358others(11): Show | 14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.1324+2618G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088112 | ||||||
| chr1:175088185
|
C | T | 1 | a0050c0054t0001g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1324+2691C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088185 | ||||||
| chr1:175088187
|
C | A | 44 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(41): Show | 44 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.1324+2693C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088187 | ||||||
| chr1:175088195
|
G | C | 3 | a0033c0072t0004g0013a0034c0070t0004g0014a0035c0071t0004g0015 | 3 | HG02622.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1324+2701G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088195 | ||||||
| chr1:175088195
|
G | T | 44 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(41): Show | 44 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.1324+2701G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088195 | ||||||
| chr1:175088240
|
T | G | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1324+2746T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088240 | ||||||
| chr1:175088437
|
C | A | 199 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(196): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1324+2943C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088437 | ||||||
| chr1:175088547
|
G | A | 110 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(107): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1324+3053G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088547 | ||||||
| chr1:175088618
|
A | G | 1 | a0002c0079t0001g0095 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1324+3124A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088618 | ||||||
| chr1:175088626
|
T | C | 200 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1324+3132T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088626 | ||||||
| chr1:175088646
|
A | G | 199 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(196): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1324+3152A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088646 | ||||||
| chr1:175088763
|
A | G | 6 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+3269A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088763 | ||||||
| chr1:175088814
|
T | G | 200 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1324+3320T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088814 | ||||||
| chr1:175088986
|
C | T | 200 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1324+3492C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175088986 | ||||||
| chr1:175089035
|
A | AC | 12 | a0004c0008t0001g0173a0004c0008t0001g0228a0004c0008t0001g0329others(9): Show | 12 | HG02015.hp2 NA18966.hp2 NA18968.hp2 others(9): Show |
intron_variant | MODIFIER | c.1324+3543dupC | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175089035 | |||||
| chr1:175089284
|
C | T | 2 | a0001c0001t0001g0164a0037c0080t0001g0165 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1324+3790C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175089284 | ||||||
| chr1:175089326
|
A | C | 39 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(36): Show | 39 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1324+3832A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175089326 | ||||||
| chr1:175089390
|
G | A | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1324+3896G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175089390 | ||||||
| chr1:175089535
|
T | G | 6 | a0010c0010t0001g0110a0010c0010t0001g0111a0010c0010t0001g0112others(3): Show | 6 | HG01243.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1324+4041T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175089535 | ||||||
| chr1:175089610
|
T | C | 2 | a0009c0021t0001g0271a0009c0021t0001g0272 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1324+4116T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175089610 | ||||||
| chr1:175089951
|
G | C | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-4039G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175089951 | ||||||
| chr1:175090147
|
C | T | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3843C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090147 | ||||||
| chr1:175090179
|
G | T | 112 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-3811G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090179 | ||||||
| chr1:175090330
|
C | G | 1 | a0038c0069t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1325-3660C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090330 | ||||||
| chr1:175090337
|
T | G | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3653T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090337 | ||||||
| chr1:175090397
|
T | C | 112 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-3593T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090397 | ||||||
| chr1:175090414
|
G | T | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3576G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090414 | ||||||
| chr1:175090418
|
C | G | 6 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-3572C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090418 | ||||||
| chr1:175090445
|
C | T | 6 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-3545C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090445 | ||||||
| chr1:175090447
|
GC | G | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3537delC | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175090447 | |||||
| chr1:175090500
|
C | T | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3490C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090500 | ||||||
| chr1:175090501
|
A | G | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3489A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090501 | ||||||
| chr1:175090502
|
G | A | 2 | a0029c0096t0001g0308a0030c0095t0003g0307 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1325-3488G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090502 | ||||||
| chr1:175090546
|
T | C | 14 | a0001c0016t0001g0355a0001c0016t0001g0356a0001c0016t0001g0358others(11): Show | 14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.1325-3444T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090546 | ||||||
| chr1:175090604
|
A | G | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3386A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090604 | ||||||
| chr1:175090610
|
C | T | 1 | a0005c0057t0001g0177 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1325-3380C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090610 | ||||||
| chr1:175090628
|
G | C | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3362G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090628 | ||||||
| chr1:175090656
|
T | C | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3334T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090656 | ||||||
| chr1:175090657
|
G | A | 3 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011 | 3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1325-3333G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090657 | ||||||
| chr1:175090706
|
G | A | 2 | a0011c0011t0001g0184a0011c0011t0001g0354 | 2 | NA18975.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1325-3284G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090706 | ||||||
| chr1:175090749
|
AATTAG | A | 5 | a0001c0001t0001g0164a0007c0006t0001g0369a0007c0006t0001g0371others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325-3238_1325-323 others(9): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175090749 | |||||
| chr1:175090841
|
T | C | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3149T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090841 | ||||||
| chr1:175090851
|
A | G | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-3139A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090851 | ||||||
| chr1:175090852
|
T | C | 112 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-3138T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175090852 | ||||||
| chr1:175091017
|
T | C | 268 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(265): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1325-2973T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091017 | ||||||
| chr1:175091147
|
C | T | 1 | a0003c0002t0001g0303 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1325-2843C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091147 | ||||||
| chr1:175091205
|
A | G | 1 | a0008c0007t0002g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1325-2785A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091205 | ||||||
| chr1:175091370
|
G | T | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-2620G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091370 | ||||||
| chr1:175091428
|
C | T | 275 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(272): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1325-2562C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091428 | ||||||
| chr1:175091546
|
T | TTTTA | 40 | a0001c0001t0001g0070a0001c0001t0001g0123a0001c0001t0001g0128others(37): Show | 41 | HG00544.hp2 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1325-2437_1325-243 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091546 | |||||
| chr1:175091555
|
TTA | T | 46 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(43): Show | 46 | HG00099.hp1 HG00438.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.1325-2433_1325-243 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091555 | |||||
| chr1:175091557
|
A | T | 114 | a0001c0001t0001g0074a0001c0001t0001g0107a0001c0001t0001g0108others(111): Show | 115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1325-2433A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091557 | ||||||
| chr1:175091558
|
T | A | 113 | a0001c0001t0001g0074a0001c0001t0001g0107a0001c0001t0001g0108others(110): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-2432T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091558 | ||||||
| chr1:175091559
|
T | A | 1 | a0002c0005t0007g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325-2431T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091559 | ||||||
| chr1:175091559
|
T | TTTTA | 34 | a0001c0042t0001g0059a0002c0029t0003g0053a0002c0029t0003g0054others(31): Show | 34 | HG00280.hp1 HG00438.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1325-2387_1325-238 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091559 | |||||
| chr1:175091559
|
T | TTTTATTT others(1): Show |
4 | a0006c0004t0001g0185a0006c0004t0001g0243a0006c0004t0001g0244others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325-2391_1325-238 others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091559 | |||||
| chr1:175091559
|
TTTTA | T | 15 | a0003c0002t0001g0302a0003c0002t0001g0305a0005c0003t0001g0230others(12): Show | 15 | HG00639.hp2 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1325-2387_1325-238 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091559 | |||||
| chr1:175091559
|
TTTTATTT others(21): Show |
T | 1 | a0004c0019t0001g0223 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1325-2411_1325-238 others(32): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091559 | |||||
| chr1:175091560
|
T | A | 46 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(43): Show | 46 | HG00099.hp1 HG00438.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.1325-2430T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091560 | ||||||
| chr1:175091561
|
T | A | 113 | a0001c0001t0001g0074a0001c0001t0001g0107a0001c0001t0001g0108others(110): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-2429T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091561 | ||||||
| chr1:175091562
|
T | A | 1 | a0002c0005t0007g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1325-2428T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091562 | ||||||
| chr1:175091563
|
A | T | 114 | a0001c0001t0001g0074a0001c0001t0001g0107a0001c0001t0001g0108others(111): Show | 115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1325-2427A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091563 | ||||||
| chr1:175091565
|
TTA | T | 39 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(36): Show | 39 | HG00099.hp1 HG00438.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1325-2423_1325-242 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091565 | |||||
| chr1:175091565
|
TTATTTA | T | 7 | a0002c0079t0001g0095a0007c0006t0001g0094a0007c0006t0001g0153others(4): Show | 7 | HG02622.hp1 HG02647.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325-2423_1325-241 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175091565 | |||||
| chr1:175091658
|
A | G | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-2332A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091658 | ||||||
| chr1:175091665
|
T | C | 39 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(36): Show | 39 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1325-2325T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091665 | ||||||
| chr1:175091683
|
G | A | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-2307G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091683 | ||||||
| chr1:175091780
|
C | G | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-2210C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091780 | ||||||
| chr1:175091781
|
G | A | 1 | a0001c0016t0001g0356 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1325-2209G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091781 | ||||||
| chr1:175091793
|
T | A | 1 | a0017c0075t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1325-2197T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091793 | ||||||
| chr1:175091810
|
G | A | 2 | a0008c0007t0002g0071a0008c0007t0002g0072 | 2 | NA18948.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1325-2180G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091810 | ||||||
| chr1:175091814
|
T | C | 1 | a0028c0033t0001g0236 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1325-2176T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091814 | ||||||
| chr1:175091825
|
A | G | 1 | a0008c0007t0002g0099 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1325-2165A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091825 | ||||||
| chr1:175091922
|
C | T | 32 | a0001c0016t0001g0040a0001c0016t0001g0355a0001c0016t0001g0356others(29): Show | 32 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1325-2068C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091922 | ||||||
| chr1:175091950
|
G | A | 10 | a0001c0001t0001g0164a0002c0005t0004g0008a0007c0006t0001g0369others(7): Show | 10 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1325-2040G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175091950 | ||||||
| chr1:175092092
|
G | T | 1 | a0005c0003t0001g0258 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1325-1898G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092092 | ||||||
| chr1:175092103
|
C | T | 1 | a0006c0063t0002g0217 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1325-1887C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092103 | ||||||
| chr1:175092236
|
T | A | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-1754T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092236 | ||||||
| chr1:175092269
|
C | T | 87 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(84): Show | 87 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(84): Show |
intron_variant | MODIFIER | c.1325-1721C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092269 | ||||||
| chr1:175092295
|
C | G | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-1695C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092295 | ||||||
| chr1:175092394
|
C | CAGACTAT others(4): Show |
201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-1587_1325-158 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175092394 | |||||
| chr1:175092451
|
G | C | 1 | a0003c0002t0001g0317 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1325-1539G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092451 | ||||||
| chr1:175092467
|
G | A | 1 | a0034c0070t0004g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1325-1523G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092467 | ||||||
| chr1:175092479
|
C | G | 1 | a0001c0001t0001g0334 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1325-1511C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092479 | ||||||
| chr1:175092523
|
C | A | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-1467C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092523 | ||||||
| chr1:175092542
|
C | A | 32 | a0001c0016t0001g0040a0001c0016t0001g0355a0001c0016t0001g0356others(29): Show | 32 | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1325-1448C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092542 | ||||||
| chr1:175092798
|
G | A | 6 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-1192G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092798 | ||||||
| chr1:175092802
|
C | A | 197 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(194): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1325-1188C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092802 | ||||||
| chr1:175092935
|
T | A | 1 | a0011c0011t0003g0189 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1325-1055T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092935 | ||||||
| chr1:175092967
|
T | G | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-1023T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092967 | ||||||
| chr1:175092973
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1325-1017C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175092973 | ||||||
| chr1:175093056
|
C | T | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-934C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093056 | ||||||
| chr1:175093103
|
A | G | 1 | a0002c0009t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1325-887A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093103 | ||||||
| chr1:175093243
|
C | A | 1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1325-747C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093243 | ||||||
| chr1:175093243
|
C | T | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1325-747C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093243 | ||||||
| chr1:175093364
|
G | T | 112 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-626G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093364 | ||||||
| chr1:175093402
|
T | C | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-588T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093402 | ||||||
| chr1:175093410
|
T | G | 5 | a0001c0001t0001g0164a0007c0006t0001g0369a0007c0006t0001g0371others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325-580T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093410 | ||||||
| chr1:175093421
|
A | G | 112 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1325-569A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093421 | ||||||
| chr1:175093528
|
A | G | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-462A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093528 | ||||||
| chr1:175093555
|
C | T | 201 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1325-435C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093555 | ||||||
| chr1:175093563
|
CTG | C | 10 | a0001c0001t0001g0164a0002c0005t0004g0008a0007c0006t0001g0369others(7): Show | 10 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1325-424_1325-423d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 175093563 | |||||
| chr1:175093582
|
A | G | 3 | a0011c0011t0001g0215a0026c0035t0001g0214a0026c0035t0001g0216 | 3 | HG00280.hp2 HG00738.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1325-408A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093582 | ||||||
| chr1:175093829
|
C | T | 1 | a0056c0052t0001g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1325-161C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093829 | ||||||
| chr1:175093858
|
G | A | 1 | a0013c0014t0001g0060 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1325-132G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 6/18 | chr1 | 175093858 | ||||||
| chr1:175094358
|
A | G | 1 | a0007c0038t0001g0367 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1588+105A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094358 | ||||||
| chr1:175094435
|
A | G | 45 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(42): Show | 45 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1588+182A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094435 | ||||||
| chr1:175094500
|
C | A | 3 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011 | 3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1588+247C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094500 | ||||||
| chr1:175094538
|
T | G | 1 | a0012c0013t0001g0073 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1588+285T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094538 | ||||||
| chr1:175094543
|
T | C | 1 | a0009c0012t0002g0326 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1588+290T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094543 | ||||||
| chr1:175094569
|
C | T | 1 | a0002c0009t0003g0362 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1588+316C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094569 | ||||||
| chr1:175094723
|
G | C | 16 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0128others(13): Show | 16 | HG01192.hp2 HG01884.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1588+470G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094723 | ||||||
| chr1:175094734
|
C | T | 1 | a0002c0009t0002g0361 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1588+481C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094734 | ||||||
| chr1:175094762
|
G | A | 3 | a0027c0034t0003g0166a0027c0034t0003g0168a0051c0066t0010g0167 | 3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1588+509G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094762 | ||||||
| chr1:175094887
|
C | T | 2 | a0005c0003t0001g0178a0005c0003t0001g0179 | 2 | NA18612.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1588+634C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094887 | ||||||
| chr1:175094905
|
G | A | 6 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1588+652G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175094905 | ||||||
| chr1:175095100
|
A | G | 1 | a0002c0005t0003g0106 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1588+847A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095100 | ||||||
| chr1:175095225
|
C | T | 125 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(122): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1588+972C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095225 | ||||||
| chr1:175095403
|
G | A | 1 | a0011c0011t0001g0190 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1588+1150G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095403 | ||||||
| chr1:175095490
|
T | C | 157 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1588+1237T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095490 | ||||||
| chr1:175095494
|
A | G | 1 | a0011c0011t0003g0189 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1588+1241A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095494 | ||||||
| chr1:175095517
|
T | G | 38 | a0001c0001t0001g0164a0001c0016t0001g0040a0001c0016t0001g0355others(35): Show | 38 | HG01081.hp1 HG01168.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.1588+1264T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095517 | ||||||
| chr1:175095617
|
A | G | 157 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1588+1364A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095617 | ||||||
| chr1:175095635
|
G | T | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1588+1382G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095635 | ||||||
| chr1:175095664
|
C | T | 6 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1588+1411C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095664 | ||||||
| chr1:175095854
|
C | T | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1589-1563C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095854 | ||||||
| chr1:175095871
|
G | A | 1 | a0003c0002t0001g0302 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1589-1546G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175095871 | ||||||
| chr1:175095917
|
CTTTTCTT others(6): Show |
C | 5 | a0001c0001t0001g0164a0007c0006t0001g0369a0007c0006t0001g0371others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589-1498_1589-148 others(17): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr1 | 175095917 | |||||
| chr1:175096266
|
G | A | 3 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011 | 3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1589-1151G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096266 | ||||||
| chr1:175096384
|
A | G | 45 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(42): Show | 45 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1589-1033A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096384 | ||||||
| chr1:175096388
|
T | G | 2 | a0001c0001t0001g0344a0001c0001t0001g0352 | 2 | HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1589-1029T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096388 | ||||||
| chr1:175096483
|
C | T | 112 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1589-934C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096483 | ||||||
| chr1:175096801
|
C | T | 6 | a0010c0010t0001g0090a0010c0010t0001g0143a0017c0025t0001g0093others(3): Show | 6 | HG00408.hp2 HG00609.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589-616C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096801 | ||||||
| chr1:175096831
|
G | A | 1 | a0038c0069t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1589-586G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096831 | ||||||
| chr1:175096937
|
G | C | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1589-480G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096937 | ||||||
| chr1:175096972
|
A | T | 5 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589-445A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096972 | ||||||
| chr1:175096974
|
A | G | 2 | a0007c0006t0001g0006a0007c0006t0001g0007 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1589-443A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175096974 | ||||||
| chr1:175097078
|
G | A | 1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1589-339G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175097078 | ||||||
| chr1:175097170
|
C | T | 10 | a0001c0016t0001g0355a0001c0016t0001g0359a0001c0028t0001g0364others(7): Show | 10 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1589-247C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175097170 | ||||||
| chr1:175097223
|
T | G | 1 | a0004c0008t0002g0171 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1589-194T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 7/18 | chr1 | 175097223 | ||||||
| chr1:175097831
|
G | A | 5 | a0001c0001t0001g0123a0001c0001t0001g0151a0001c0001t0002g0122others(2): Show | 5 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1855+148G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/18 | chr1 | 175097831 | ||||||
| chr1:175097985
|
T | C | 1 | a0027c0034t0003g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1855+302T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/18 | chr1 | 175097985 | ||||||
| chr1:175098001
|
C | G | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1855+318C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/18 | chr1 | 175098001 | ||||||
| chr1:175098043
|
G | C | 1 | a0001c0001t0001g0344 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1856-289G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/18 | chr1 | 175098043 | ||||||
| chr1:175098092
|
G | A | 1 | a0001c0016t0001g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1856-240G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 8/18 | chr1 | 175098092 | ||||||
| chr1:175098719
|
TAC | T | 6 | a0007c0006t0001g0006a0007c0006t0001g0007a0027c0034t0003g0166others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2119+126_2119+127d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175098719 | |||||
| chr1:175098875
|
T | A | 197 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(194): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2119+280T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175098875 | ||||||
| chr1:175099070
|
A | T | 1 | a0038c0069t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2119+475A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099070 | ||||||
| chr1:175099175
|
T | C | 2 | a0029c0096t0001g0308a0030c0095t0003g0307 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2119+580T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099175 | ||||||
| chr1:175099417
|
G | A | 112 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.2119+822G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099417 | ||||||
| chr1:175099461
|
A | C | 42 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(39): Show | 42 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.2119+866A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099461 | ||||||
| chr1:175099570
|
AGAGGAGA others(39): Show |
A | 45 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(42): Show | 45 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.2119+984_2119+1029 others(49): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175099570 | |||||
| chr1:175099586
|
C | CTCAGGAG others(16): Show |
6 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2119+1047_2119+106 others(27): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175099586 | |||||
| chr1:175099586
|
CTCAGGAG others(16): Show |
C | 128 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(125): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2119+1047_2119+106 others(27): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175099586 | |||||
| chr1:175099588
|
CAGG | C | 5 | a0001c0001t0001g0164a0007c0006t0001g0369a0007c0006t0001g0371others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2119+1002_2119+100 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175099588 | |||||
| chr1:175099629
|
G | A | 1 | a0045c0088t0001g0114 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2119+1034G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099629 | ||||||
| chr1:175099855
|
G | A | 1 | a0011c0011t0001g0354 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2119+1260G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099855 | ||||||
| chr1:175099929
|
G | A | 5 | a0003c0002t0001g0283a0003c0002t0001g0317a0003c0002t0012g0277others(2): Show | 5 | HG02698.hp1 HG02735.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.2119+1334G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099929 | ||||||
| chr1:175099938
|
T | C | 3 | a0019c0023t0001g0309a0022c0058t0006g0274a0022c0060t0006g0316 | 3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2119+1343T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099938 | ||||||
| chr1:175099964
|
A | G | 3 | a0019c0023t0001g0309a0022c0058t0006g0274a0022c0060t0006g0316 | 3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2119+1369A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099964 | ||||||
| chr1:175099986
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2119+1391G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175099986 | ||||||
| chr1:175100234
|
T | A | 25 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0123others(22): Show | 25 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.2119+1639T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100234 | ||||||
| chr1:175100287
|
C | T | 12 | a0001c0016t0001g0040a0002c0009t0001g0036a0002c0009t0001g0037others(9): Show | 12 | HG01081.hp1 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2119+1692C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100287 | ||||||
| chr1:175100372
|
A | T | 9 | a0013c0014t0001g0056a0013c0014t0001g0060a0013c0014t0001g0065others(6): Show | 9 | HG01358.hp1 HG01891.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.2119+1777A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100372 | ||||||
| chr1:175100414
|
G | C | 1 | a0015c0092t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2119+1819G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100414 | ||||||
| chr1:175100433
|
C | T | 1 | a0015c0092t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2119+1838C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100433 | ||||||
| chr1:175100661
|
C | T | 1 | a0006c0004t0001g0213 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2119+2066C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100661 | ||||||
| chr1:175100669
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2119+2074G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100669 | ||||||
| chr1:175100672
|
A | G | 5 | a0005c0003t0001g0212a0005c0003t0001g0257a0005c0003t0002g0210others(2): Show | 5 | HG01255.hp2 HG01361.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.2119+2077A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100672 | ||||||
| chr1:175100700
|
GT | G | 164 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(161): Show | 166 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2119+2116delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175100700 | |||||
| chr1:175100700
|
GTT | G | 61 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2119+2115_2119+211 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175100700 | |||||
| chr1:175100757
|
A | G | 68 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(65): Show | 69 | HG00099.hp2 HG00438.hp1 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.2119+2162A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100757 | ||||||
| chr1:175100783
|
TCAA | T | 3 | a0019c0023t0001g0309a0022c0058t0006g0274a0022c0060t0006g0316 | 3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2119+2192_2119+219 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175100783 | |||||
| chr1:175100849
|
T | C | 2 | a0024c0039t0009g0010a0024c0039t0009g0012 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2119+2254T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100849 | ||||||
| chr1:175100878
|
A | G | 14 | a0001c0016t0001g0355a0001c0016t0001g0356a0001c0016t0001g0358others(11): Show | 14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2119+2283A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100878 | ||||||
| chr1:175100953
|
A | C | 1 | a0003c0002t0001g0300 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2119+2358A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100953 | ||||||
| chr1:175100998
|
T | TGCAAACC others(3438): Show |
1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2403_2119+240 others(3449): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175100998 | ||||||
| chr1:175101003
|
T | G | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2408T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101003 | ||||||
| chr1:175101004
|
T | G | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2409T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101004 | ||||||
| chr1:175101005
|
A | G | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2410A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101005 | ||||||
| chr1:175101007
|
A | C | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2412A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101007 | ||||||
| chr1:175101009
|
A | G | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2414A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101009 | ||||||
| chr1:175101011
|
A | T | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2416A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101011 | ||||||
| chr1:175101018
|
A | T | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2423A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101018 | ||||||
| chr1:175101023
|
C | T | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2428C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101023 | ||||||
| chr1:175101025
|
C | G | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2430C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101025 | ||||||
| chr1:175101026
|
T | G | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2431T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101026 | ||||||
| chr1:175101027
|
T | A | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2432T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101027 | ||||||
| chr1:175101029
|
T | A | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2434T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101029 | ||||||
| chr1:175101031
|
G | T | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2436G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101031 | ||||||
| chr1:175101034
|
A | T | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2439A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101034 | ||||||
| chr1:175101039
|
G | A | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2444G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101039 | ||||||
| chr1:175101042
|
A | G | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2447A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101042 | ||||||
| chr1:175101046
|
A | C | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2451A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101046 | ||||||
| chr1:175101049
|
A | G | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2454A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101049 | ||||||
| chr1:175101054
|
T | G | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2459T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101054 | ||||||
| chr1:175101057
|
T | C | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2462T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101057 | ||||||
| chr1:175101060
|
T | A | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2465T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101060 | ||||||
| chr1:175101064
|
C | CAAGCCGT others(2577): Show |
1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2469_2119+247 others(2588): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101064 | ||||||
| chr1:175101065
|
T | G | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2470T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101065 | ||||||
| chr1:175101068
|
A | C | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2473A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101068 | ||||||
| chr1:175101070
|
T | C | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2475T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101070 | ||||||
| chr1:175101073
|
T | A | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2478T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101073 | ||||||
| chr1:175101074
|
C | A | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2479C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101074 | ||||||
| chr1:175101075
|
C | A | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2480C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101075 | ||||||
| chr1:175101082
|
C | T | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2487C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101082 | ||||||
| chr1:175101118
|
A | G | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2523A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101118 | ||||||
| chr1:175101126
|
T | C | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2531T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101126 | ||||||
| chr1:175101129
|
G | A | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2534G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101129 | ||||||
| chr1:175101130
|
G | A | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2535G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101130 | ||||||
| chr1:175101138
|
C | T | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2543C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101138 | ||||||
| chr1:175101186
|
G | C | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2591G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101186 | ||||||
| chr1:175101204
|
C | T | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2609C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101204 | ||||||
| chr1:175101236
|
T | TTGCTGGC others(117): Show |
1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2641_2119+264 others(128): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101236 | ||||||
| chr1:175101237
|
C | G | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2642C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101237 | ||||||
| chr1:175101250
|
A | C | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2655A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101250 | ||||||
| chr1:175101275
|
G | A | 1 | a0056c0052t0001g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2119+2680G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101275 | ||||||
| chr1:175101276
|
C | T | 2 | a0001c0089t0001g0024a0022c0059t0001g0175 | 2 | HG01069.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2119+2681C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101276 | ||||||
| chr1:175101304
|
G | A | 3 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011 | 3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2119+2709G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101304 | ||||||
| chr1:175101305
|
C | T | 1 | a0011c0011t0001g0184 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2119+2710C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101305 | ||||||
| chr1:175101319
|
G | C | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2724G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101319 | ||||||
| chr1:175101329
|
G | A | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2734G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101329 | ||||||
| chr1:175101338
|
G | A | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2743G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101338 | ||||||
| chr1:175101345
|
C | T | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+2750C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101345 | ||||||
| chr1:175101378
|
C | T | 1 | a0011c0011t0003g0189 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2119+2783C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101378 | ||||||
| chr1:175101379
|
G | GGTGA | 88 | a0003c0002t0001g0266a0003c0002t0001g0270a0003c0002t0001g0278others(85): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.2119+2787_2119+278 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175101379 | |||||
| chr1:175101434
|
T | C | 14 | a0001c0016t0001g0355a0001c0016t0001g0356a0001c0016t0001g0358others(11): Show | 14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2119+2839T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101434 | ||||||
| chr1:175101446
|
C | T | 3 | a0027c0034t0003g0166a0027c0034t0003g0168a0051c0066t0010g0167 | 3 | HG02109.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2119+2851C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101446 | ||||||
| chr1:175101482
|
C | G | 1 | a0004c0019t0001g0209 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2119+2887C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101482 | ||||||
| chr1:175101483
|
G | A | 2 | a0003c0002t0001g0278a0009c0021t0001g0276 | 2 | HG00280.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2119+2888G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101483 | ||||||
| chr1:175101524
|
G | C | 232 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2119+2929G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101524 | ||||||
| chr1:175101529
|
T | G | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2119+2934T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101529 | ||||||
| chr1:175101600
|
G | A | 10 | a0001c0001t0001g0164a0007c0006t0001g0369a0007c0006t0001g0371others(7): Show | 10 | HG02145.hp1 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2119+3005G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101600 | ||||||
| chr1:175101714
|
G | A | 1 | a0028c0033t0001g0183 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2119+3119G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101714 | ||||||
| chr1:175101765
|
G | T | 46 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(43): Show | 46 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.2119+3170G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101765 | ||||||
| chr1:175101812
|
A | G | 3 | a0006c0004t0001g0185a0011c0011t0001g0184a0011c0011t0001g0354 | 3 | NA18975.hp1 NA19006.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2119+3217A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101812 | ||||||
| chr1:175101812
|
ACCAGAGC others(6151): Show |
A | 89 | a0003c0002t0001g0266a0003c0002t0001g0270a0003c0002t0001g0278others(86): Show | 90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.2119+3330_2120-885 others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175101812 | |||||
| chr1:175101925
|
A | G | 59 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(56): Show | 59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+3330A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101925 | ||||||
| chr1:175101932
|
A | T | 59 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(56): Show | 59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+3337A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101932 | ||||||
| chr1:175101959
|
C | T | 1 | a0007c0006t0004g0009 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2119+3364C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101959 | ||||||
| chr1:175101966
|
G | A | 4 | a0001c0042t0001g0059a0002c0026t0001g0001a0002c0026t0003g0062others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2119+3371G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175101966 | ||||||
| chr1:175102075
|
A | G | 1 | a0002c0009t0002g0361 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2119+3480A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102075 | ||||||
| chr1:175102216
|
CT | C | 3 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011 | 3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2119+3622delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102216 | ||||||
| chr1:175102287
|
G | A | 1 | a0006c0004t0001g0253 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2119+3692G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102287 | ||||||
| chr1:175102288
|
C | T | 1 | a0005c0003t0001g0255 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2119+3693C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102288 | ||||||
| chr1:175102324
|
G | A | 1 | a0001c0001t0001g0334 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2119+3729G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102324 | ||||||
| chr1:175102420
|
G | A | 5 | a0001c0016t0001g0356a0001c0016t0001g0358a0002c0009t0002g0361others(2): Show | 5 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.2119+3825G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102420 | ||||||
| chr1:175102432
|
C | T | 59 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(56): Show | 59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+3837C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102432 | ||||||
| chr1:175102491
|
G | C | 14 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(11): Show | 15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2119+3896G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102491 | ||||||
| chr1:175102620
|
C | A | 1 | a0001c0082t0008g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2119+4025C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102620 | ||||||
| chr1:175102642
|
G | A | 1 | a0002c0009t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2119+4047G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102642 | ||||||
| chr1:175102649
|
C | A | 3 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011 | 3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2119+4054C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102649 | ||||||
| chr1:175102662
|
T | C | 147 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(144): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2119+4067T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102662 | ||||||
| chr1:175102687
|
C | A | 1 | a0001c0001t0001g0351 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2119+4092C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102687 | ||||||
| chr1:175102725
|
T | C | 14 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(11): Show | 15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2119+4130T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102725 | ||||||
| chr1:175102740
|
G | A | 2 | a0019c0023t0001g0309a0022c0058t0006g0274 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2119+4145G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102740 | ||||||
| chr1:175102764
|
A | G | 147 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(144): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2119+4169A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102764 | ||||||
| chr1:175102880
|
C | T | 3 | a0019c0023t0001g0309a0022c0058t0006g0274a0022c0060t0006g0316 | 3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2119+4285C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102880 | ||||||
| chr1:175102988
|
A | G | 1 | a0001c0074t0001g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2119+4393A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175102988 | ||||||
| chr1:175103156
|
G | A | 39 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.2119+4561G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103156 | ||||||
| chr1:175103248
|
G | A | 1 | a0008c0007t0002g0132 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2119+4653G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103248 | ||||||
| chr1:175103492
|
A | C | 59 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(56): Show | 59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+4897A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103492 | ||||||
| chr1:175103565
|
G | GCTGTTTT others(3648): Show |
1 | a0002c0029t0001g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2119+4984_2119+498 others(3659): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175103565 | |||||
| chr1:175103565
|
G | GCTGTTTT others(3599): Show |
2 | a0002c0029t0003g0053a0002c0029t0003g0054 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2119+4984_2119+498 others(3610): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175103565 | |||||
| chr1:175103637
|
T | C | 1 | a0055c0049t0002g0262 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2119+5042T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103637 | ||||||
| chr1:175103641
|
C | T | 1 | a0019c0023t0001g0241 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2119+5046C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103641 | ||||||
| chr1:175103653
|
C | A | 5 | a0001c0001t0001g0164a0007c0006t0001g0369a0007c0006t0001g0371others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2119+5058C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103653 | ||||||
| chr1:175103696
|
T | C | 3 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011 | 3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2119+5101T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103696 | ||||||
| chr1:175103812
|
C | T | 4 | a0002c0029t0001g0055a0002c0029t0003g0053a0002c0029t0003g0054others(1): Show | 4 | HG01257.hp2 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2119+5217C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103812 | ||||||
| chr1:175103912
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2119+5317G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175103912 | ||||||
| chr1:175104222
|
A | G | 1 | a0038c0069t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2119+5627A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104222 | ||||||
| chr1:175104231
|
G | C | 1 | a0001c0001t0001g0031 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2119+5636G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104231 | ||||||
| chr1:175104391
|
A | G | 73 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(70): Show | 73 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(70): Show |
intron_variant | MODIFIER | c.2119+5796A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104391 | ||||||
| chr1:175104666
|
G | T | 1 | a0004c0008t0002g0208 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2119+6071G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104666 | ||||||
| chr1:175104670
|
C | T | 2 | a0002c0005t0007g0057a0002c0079t0001g0095 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2119+6075C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104670 | ||||||
| chr1:175104764
|
A | G | 1 | a0007c0006t0004g0009 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2119+6169A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104764 | ||||||
| chr1:175104961
|
G | A | 3 | a0019c0023t0001g0309a0022c0058t0006g0274a0022c0060t0006g0316 | 3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2119+6366G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175104961 | ||||||
| chr1:175105012
|
G | A | 2 | a0002c0005t0007g0057a0002c0079t0001g0095 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2119+6417G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105012 | ||||||
| chr1:175105072
|
C | T | 1 | a0008c0007t0002g0058 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2119+6477C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105072 | ||||||
| chr1:175105303
|
G | A | 3 | a0002c0005t0001g0119a0002c0005t0003g0149a0002c0005t0003g0150 | 3 | HG00140.hp1 HG02257.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2119+6708G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105303 | ||||||
| chr1:175105350
|
C | T | 3 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011 | 3 | HG01891.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2119+6755C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105350 | ||||||
| chr1:175105527
|
G | A | 2 | a0001c0042t0001g0097a0036c0090t0005g0102 | 2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2119+6932G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105527 | ||||||
| chr1:175105641
|
G | A | 14 | a0001c0016t0001g0355a0001c0016t0001g0356a0001c0016t0001g0358others(11): Show | 14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2119+7046G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105641 | ||||||
| chr1:175105669
|
A | C | 3 | a0007c0006t0001g0369a0007c0006t0001g0371a0014c0024t0001g0370 | 3 | HG02886.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2119+7074A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105669 | ||||||
| chr1:175105686
|
G | A | 1 | a0006c0004t0001g0218 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2119+7091G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105686 | ||||||
| chr1:175105820
|
A | G | 144 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(141): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.2119+7225A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105820 | ||||||
| chr1:175105881
|
T | C | 5 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0031t0005g0156others(2): Show | 5 | HG01192.hp2 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2119+7286T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175105881 | ||||||
| chr1:175106029
|
G | C | 1 | a0007c0006t0001g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2119+7434G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106029 | ||||||
| chr1:175106043
|
G | A | 14 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(11): Show | 15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2119+7448G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106043 | ||||||
| chr1:175106073
|
G | A | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2119+7478G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106073 | ||||||
| chr1:175106141
|
G | A | 1 | a0001c0031t0005g0075 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2119+7546G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106141 | ||||||
| chr1:175106150
|
T | C | 59 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(56): Show | 59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+7555T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106150 | ||||||
| chr1:175106168
|
C | T | 3 | a0007c0006t0001g0006a0007c0006t0001g0007a0039c0078t0003g0005 | 3 | HG02109.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2119+7573C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106168 | ||||||
| chr1:175106215
|
A | T | 3 | a0005c0003t0001g0188a0006c0004t0001g0185a0006c0004t0001g0253 | 3 | HG00438.hp2 HG02155.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2119+7620A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106215 | ||||||
| chr1:175106257
|
A | C | 5 | a0001c0016t0001g0356a0001c0016t0001g0358a0002c0009t0002g0361others(2): Show | 5 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.2119+7662A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106257 | ||||||
| chr1:175106277
|
G | A | 60 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2119+7682G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106277 | ||||||
| chr1:175106356
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2119+7761A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106356 | ||||||
| chr1:175106478
|
C | T | 5 | a0001c0001t0001g0164a0007c0006t0001g0369a0007c0006t0001g0371others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2119+7883C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106478 | ||||||
| chr1:175106514
|
A | T | 14 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(11): Show | 15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2119+7919A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106514 | ||||||
| chr1:175106623
|
G | T | 59 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(56): Show | 59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+8028G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106623 | ||||||
| chr1:175106690
|
G | A | 56 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(53): Show | 56 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.2119+8095G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106690 | ||||||
| chr1:175106740
|
G | C | 11 | a0001c0042t0001g0059a0001c0042t0001g0097a0002c0005t0007g0057others(8): Show | 12 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2119+8145G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106740 | ||||||
| chr1:175106742
|
C | T | 3 | a0019c0023t0001g0170a0019c0023t0001g0174a0019c0023t0001g0241 | 3 | HG02486.hp1 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2119+8147C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106742 | ||||||
| chr1:175106758
|
C | T | 14 | a0001c0016t0001g0355a0001c0016t0001g0356a0001c0016t0001g0358others(11): Show | 14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2119+8163C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106758 | ||||||
| chr1:175106835
|
C | T | 1 | a0002c0009t0001g0042 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2119+8240C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106835 | ||||||
| chr1:175106918
|
G | A | 1 | a0007c0006t0001g0371 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2119+8323G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106918 | ||||||
| chr1:175106950
|
G | A | 1 | a0001c0016t0001g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2119+8355G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106950 | ||||||
| chr1:175106992
|
G | A | 1 | a0005c0003t0001g0186 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2119+8397G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175106992 | ||||||
| chr1:175107028
|
C | T | 16 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0001g0334others(13): Show | 17 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2119+8433C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107028 | ||||||
| chr1:175107066
|
C | T | 4 | a0002c0005t0003g0103a0002c0005t0003g0105a0002c0005t0003g0106others(1): Show | 4 | HG01192.hp1 HG01943.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2119+8471C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107066 | ||||||
| chr1:175107080
|
C | T | 1 | a0008c0007t0002g0142 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2119+8485C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107080 | ||||||
| chr1:175107092
|
C | T | 13 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0128others(10): Show | 13 | HG01192.hp2 HG01884.hp1 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.2119+8497C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107092 | ||||||
| chr1:175107112
|
C | T | 60 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2119+8517C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107112 | ||||||
| chr1:175107164
|
C | CTCGTGGT others(124): Show |
1 | a0002c0005t0004g0008 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2119+8630_2119+876 others(135): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175107164 | |||||
| chr1:175107164
|
CTCGTGGT others(124): Show |
C | 2 | a0005c0003t0001g0212a0005c0003t0001g0257 | 2 | HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2119+8630_2119+876 others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175107164 | |||||
| chr1:175107167
|
G | A | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2119+8572G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107167 | ||||||
| chr1:175107288
|
G | A | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2119+8693G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107288 | ||||||
| chr1:175107298
|
G | A | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2119+8703G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107298 | ||||||
| chr1:175107301
|
G | T | 1 | a0027c0034t0003g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2119+8706G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107301 | ||||||
| chr1:175107325
|
G | A | 1 | a0007c0006t0001g0153 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2119+8730G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107325 | ||||||
| chr1:175107327
|
G | A | 14 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(11): Show | 15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2119+8732G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107327 | ||||||
| chr1:175107344
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2119+8749C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107344 | ||||||
| chr1:175107394
|
G | T | 11 | a0001c0016t0001g0040a0002c0009t0001g0036a0002c0009t0001g0037others(8): Show | 11 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2119+8799G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107394 | ||||||
| chr1:175107458
|
A | G | 147 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(144): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2119+8863A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107458 | ||||||
| chr1:175107474
|
G | A | 6 | a0001c0001t0001g0070a0001c0001t0001g0158a0001c0001t0001g0160others(3): Show | 6 | HG01192.hp2 HG01884.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2119+8879G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107474 | ||||||
| chr1:175107475
|
T | A | 2 | a0001c0001t0001g0164a0037c0080t0001g0165 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2119+8880T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107475 | ||||||
| chr1:175107492
|
A | G | 59 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(56): Show | 59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+8897A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107492 | ||||||
| chr1:175107499
|
T | C | 14 | a0001c0016t0001g0355a0001c0016t0001g0356a0001c0016t0001g0358others(11): Show | 14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2119+8904T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107499 | ||||||
| chr1:175107561
|
G | A | 1 | a0040c0077t0001g0348 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2119+8966G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107561 | ||||||
| chr1:175107646
|
G | T | 1 | a0001c0001t0001g0336 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2119+9051G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107646 | ||||||
| chr1:175107682
|
G | C | 143 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.2119+9087G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107682 | ||||||
| chr1:175107687
|
T | G | 59 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(56): Show | 59 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.2119+9092T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107687 | ||||||
| chr1:175107745
|
C | T | 2 | a0011c0011t0001g0184a0011c0011t0001g0354 | 2 | NA18975.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2119+9150C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107745 | ||||||
| chr1:175107934
|
A | G | 1 | a0002c0009t0003g0362 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2120-9005A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107934 | ||||||
| chr1:175107970
|
G | A | 147 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(144): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2120-8969G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175107970 | ||||||
| chr1:175108048
|
T | C | 1 | a0001c0001t0001g0346 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2120-8891T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108048 | ||||||
| chr1:175108077
|
C | CGATTGAT others(6151): Show |
1 | a0002c0005t0002g0116 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2120-8857_2120-885 others(6162): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175108077 | |||||
| chr1:175108077
|
C | T | 59 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.2120-8862C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108077 | ||||||
| chr1:175108080
|
T | C | 1 | a0017c0075t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2120-8859T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108080 | ||||||
| chr1:175108131
|
C | T | 1 | a0007c0006t0001g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2120-8808C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108131 | ||||||
| chr1:175108148
|
G | A | 5 | a0001c0001t0001g0164a0007c0006t0001g0369a0007c0006t0001g0371others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-8791G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108148 | ||||||
| chr1:175108148
|
G | GGAGTGTT others(112): Show |
1 | a0012c0013t0001g0101 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2120-8755_2120-863 others(123): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175108148 | |||||
| chr1:175108151
|
G | C | 1 | a0007c0006t0001g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2120-8788G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108151 | ||||||
| chr1:175108155
|
T | C | 5 | a0001c0001t0001g0164a0007c0006t0001g0369a0007c0006t0001g0371others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-8784T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108155 | ||||||
| chr1:175108194
|
G | C | 1 | a0006c0004t0001g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2120-8745G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108194 | ||||||
| chr1:175108233
|
G | A | 19 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(16): Show | 20 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2120-8706G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108233 | ||||||
| chr1:175108233
|
G | C | 87 | a0003c0002t0001g0266a0003c0002t0001g0270a0003c0002t0001g0278others(84): Show | 88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2120-8706G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108233 | ||||||
| chr1:175108324
|
T | C | 14 | a0001c0016t0001g0355a0001c0016t0001g0356a0001c0016t0001g0358others(11): Show | 14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2120-8615T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108324 | ||||||
| chr1:175108334
|
C | T | 5 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-8605C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108334 | ||||||
| chr1:175108397
|
G | C | 236 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(233): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2120-8542G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108397 | ||||||
| chr1:175108463
|
G | C | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8476G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108463 | ||||||
| chr1:175108481
|
G | A | 1 | a0023c0043t0001g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2120-8458G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108481 | ||||||
| chr1:175108494
|
G | A | 1 | a0003c0015t0003g0265 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2120-8445G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108494 | ||||||
| chr1:175108520
|
T | C | 14 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(11): Show | 15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2120-8419T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108520 | ||||||
| chr1:175108531
|
G | A | 1 | a0004c0019t0001g0209 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2120-8408G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108531 | ||||||
| chr1:175108538
|
A | G | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8401A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108538 | ||||||
| chr1:175108539
|
C | G | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2120-8400C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108539 | ||||||
| chr1:175108549
|
C | T | 2 | a0019c0023t0001g0170a0019c0023t0001g0174 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2120-8390C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108549 | ||||||
| chr1:175108577
|
G | A | 9 | a0013c0014t0001g0056a0013c0014t0001g0060a0013c0014t0001g0065others(6): Show | 9 | HG01358.hp1 HG01891.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.2120-8362G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108577 | ||||||
| chr1:175108594
|
C | T | 1 | a0002c0009t0001g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2120-8345C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108594 | ||||||
| chr1:175108722
|
G | A | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8217G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108722 | ||||||
| chr1:175108799
|
G | A | 7 | a0001c0016t0001g0359a0001c0028t0001g0364a0002c0009t0003g0357others(4): Show | 7 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2120-8140G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108799 | ||||||
| chr1:175108811
|
T | C | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8128T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108811 | ||||||
| chr1:175108819
|
T | C | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8120T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108819 | ||||||
| chr1:175108827
|
G | A | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8112G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108827 | ||||||
| chr1:175108831
|
A | G | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-8108A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108831 | ||||||
| chr1:175108833
|
G | A | 1 | a0002c0009t0002g0361 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2120-8106G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108833 | ||||||
| chr1:175108906
|
A | C | 1 | a0001c0001t0001g0351 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2120-8033A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108906 | ||||||
| chr1:175108946
|
A | G | 3 | a0002c0029t0001g0055a0002c0029t0003g0053a0002c0029t0003g0054 | 3 | HG02630.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2120-7993A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175108946 | ||||||
| chr1:175109008
|
C | T | 5 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-7931C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109008 | ||||||
| chr1:175109072
|
A | AT | 24 | a0002c0005t0004g0008a0003c0002t0001g0310a0003c0002t0001g0313others(21): Show | 24 | HG01255.hp2 HG01361.hp2 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.2120-7840dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATT | 61 | a0003c0002t0001g0266a0003c0002t0001g0278a0003c0002t0001g0279others(58): Show | 62 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.2120-7841_2120-784 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTT | 9 | a0003c0002t0001g0303a0003c0002t0001g0322a0003c0015t0003g0265others(6): Show | 9 | HG00609.hp1 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2120-7842_2120-784 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(1): Show |
14 | a0001c0001t0001g0107a0002c0005t0002g0116a0002c0005t0003g0103others(11): Show | 14 | HG01069.hp1 HG01192.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.2120-7847_2120-784 others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(2): Show |
12 | a0001c0016t0001g0040a0001c0074t0001g0052a0002c0009t0001g0036others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2120-7848_2120-784 others(13): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(3): Show |
3 | a0019c0023t0001g0309a0022c0058t0006g0274a0022c0060t0006g0316 | 3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2120-7849_2120-784 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(4): Show |
4 | a0014c0024t0001g0161a0014c0024t0001g0162a0019c0023t0001g0170others(1): Show | 4 | HG02615.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2120-7850_2120-784 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(5): Show |
7 | a0001c0001t0001g0074a0001c0001t0001g0338a0001c0001t0001g0343others(4): Show | 7 | HG01346.hp2 HG02486.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2120-7851_2120-784 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(6): Show |
24 | a0001c0001t0001g0020a0001c0001t0001g0070a0001c0001t0001g0128others(21): Show | 24 | HG00099.hp2 HG01106.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.2120-7852_2120-784 others(17): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(7): Show |
12 | a0001c0001t0001g0023a0001c0001t0001g0331a0001c0001t0001g0351others(9): Show | 12 | HG01167.hp1 HG01358.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.2120-7853_2120-784 others(18): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(8): Show |
3 | a0001c0001t0001g0031a0001c0001t0001g0336a0014c0030t0001g0050 | 3 | HG02300.hp2 HG02738.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2120-7854_2120-784 others(19): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0332a0002c0005t0002g0342 | 2 | HG02135.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2120-7855_2120-784 others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(10): Show |
2 | a0001c0001t0001g0160a0001c0001t0001g0334 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2120-7856_2120-784 others(21): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(11): Show |
1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2120-7857_2120-784 others(22): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(12): Show |
4 | a0007c0006t0001g0006a0007c0006t0001g0117a0007c0006t0001g0120others(1): Show | 4 | HG02738.hp1 HG02895.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.2120-7858_2120-784 others(23): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(13): Show |
2 | a0007c0006t0001g0007a0007c0006t0001g0118 | 2 | HG02897.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.2120-7859_2120-784 others(24): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(14): Show |
1 | a0002c0005t0016g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2120-7860_2120-784 others(25): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(17): Show |
1 | a0002c0005t0003g0149 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2120-7863_2120-784 others(28): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(18): Show |
3 | a0001c0001t0001g0123a0001c0001t0001g0323a0002c0005t0001g0121 | 3 | HG00323.hp2 HG01081.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2120-7864_2120-784 others(29): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(19): Show |
1 | a0001c0001t0001g0151 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2120-7865_2120-784 others(30): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(20): Show |
3 | a0001c0001t0001g0324a0001c0001t0002g0122a0001c0001t0002g0163 | 3 | HG00099.hp1 HG01123.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2120-7866_2120-784 others(31): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(21): Show |
1 | a0001c0001t0001g0108 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2120-7840_2120-783 others(32): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(22): Show |
2 | a0002c0005t0003g0150a0007c0006t0001g0115 | 2 | HG02257.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2120-7840_2120-783 others(33): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
A | ATTTTTTT others(23): Show |
1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2120-7840_2120-783 others(34): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
AT | A | 6 | a0001c0031t0005g0075a0004c0008t0002g0239a0005c0003t0001g0181others(3): Show | 6 | HG01258.hp2 HG03041.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.2120-7840delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
ATTTTTTT others(2): Show |
A | 13 | a0001c0016t0001g0356a0001c0016t0001g0358a0001c0016t0001g0359others(10): Show | 13 | HG01081.hp1 HG01261.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.2120-7848_2120-784 others(13): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0016t0001g0355a0002c0009t0002g0363 | 2 | HG01168.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2120-7849_2120-784 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109072
|
ATTTTTTT others(7): Show |
A | 14 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(11): Show | 15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2120-7853_2120-784 others(18): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175109072 | |||||
| chr1:175109121
|
G | A | 1 | a0014c0030t0001g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2120-7818G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109121 | ||||||
| chr1:175109130
|
G | A | 60 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2120-7809G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109130 | ||||||
| chr1:175109136
|
C | T | 1 | a0022c0059t0001g0175 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2120-7803C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109136 | ||||||
| chr1:175109149
|
C | T | 3 | a0033c0072t0004g0013a0034c0070t0004g0014a0035c0071t0004g0015 | 3 | HG02622.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2120-7790C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109149 | ||||||
| chr1:175109234
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2120-7705G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109234 | ||||||
| chr1:175109238
|
G | A | 5 | a0002c0005t0007g0057a0002c0079t0001g0095a0027c0034t0003g0166others(2): Show | 5 | HG02109.hp2 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-7701G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109238 | ||||||
| chr1:175109243
|
C | T | 2 | a0002c0005t0007g0057a0002c0079t0001g0095 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2120-7696C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109243 | ||||||
| chr1:175109245
|
C | T | 14 | a0001c0016t0001g0355a0001c0016t0001g0356a0001c0016t0001g0358others(11): Show | 14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2120-7694C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109245 | ||||||
| chr1:175109249
|
C | T | 10 | a0004c0008t0001g0173a0004c0008t0001g0228a0004c0008t0001g0329others(7): Show | 10 | HG02015.hp2 NA18966.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.2120-7690C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109249 | ||||||
| chr1:175109278
|
C | T | 1 | a0007c0006t0001g0061 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2120-7661C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109278 | ||||||
| chr1:175109279
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2120-7660G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109279 | ||||||
| chr1:175109310
|
G | A | 1 | a0011c0011t0001g0240 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2120-7629G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109310 | ||||||
| chr1:175109329
|
G | C | 232 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2120-7610G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109329 | ||||||
| chr1:175109339
|
C | T | 94 | a0001c0016t0001g0355a0002c0005t0004g0008a0003c0002t0001g0266others(91): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.2120-7600C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109339 | ||||||
| chr1:175109377
|
C | T | 3 | a0002c0029t0001g0055a0002c0029t0003g0053a0002c0029t0003g0054 | 3 | HG02630.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2120-7562C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109377 | ||||||
| chr1:175109383
|
C | T | 1 | a0003c0002t0001g0292 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2120-7556C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109383 | ||||||
| chr1:175109384
|
G | A | 2 | a0001c0001t0001g0074a0001c0082t0008g0131 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2120-7555G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109384 | ||||||
| chr1:175109462
|
C | T | 370 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(367): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2120-7477C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109462 | ||||||
| chr1:175109542
|
T | C | 5 | a0001c0074t0001g0052a0002c0029t0001g0055a0002c0029t0003g0053others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-7397T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109542 | ||||||
| chr1:175109674
|
T | A | 2 | a0002c0005t0007g0057a0002c0079t0001g0095 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2120-7265T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109674 | ||||||
| chr1:175109675
|
A | T | 2 | a0002c0005t0007g0057a0002c0079t0001g0095 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2120-7264A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109675 | ||||||
| chr1:175109722
|
A | G | 14 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(11): Show | 15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2120-7217A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109722 | ||||||
| chr1:175109891
|
A | G | 87 | a0003c0002t0001g0266a0003c0002t0001g0270a0003c0002t0001g0278others(84): Show | 88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2120-7048A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175109891 | ||||||
| chr1:175110015
|
C | G | 11 | a0001c0016t0001g0040a0002c0009t0001g0036a0002c0009t0001g0037others(8): Show | 11 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2120-6924C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110015 | ||||||
| chr1:175110110
|
T | C | 3 | a0019c0023t0001g0309a0022c0058t0006g0274a0022c0060t0006g0316 | 3 | HG02145.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2120-6829T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110110 | ||||||
| chr1:175110125
|
C | T | 14 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(11): Show | 15 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2120-6814C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110125 | ||||||
| chr1:175110234
|
A | G | 3 | a0001c0016t0001g0040a0002c0009t0001g0036a0002c0009t0001g0041 | 3 | HG02257.hp2 HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2120-6705A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110234 | ||||||
| chr1:175110498
|
A | G | 56 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(53): Show | 56 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.2120-6441A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110498 | ||||||
| chr1:175110528
|
T | C | 1 | a0016c0020t0001g0078 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2120-6411T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110528 | ||||||
| chr1:175110746
|
T | G | 2 | a0029c0096t0001g0308a0030c0095t0003g0307 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2120-6193T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110746 | ||||||
| chr1:175110883
|
T | G | 149 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.2120-6056T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175110883 | ||||||
| chr1:175111050
|
G | A | 8 | a0003c0002t0001g0266a0003c0015t0001g0264a0003c0015t0001g0312others(5): Show | 8 | NA18955.hp2 NA18969.hp1 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.2120-5889G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111050 | ||||||
| chr1:175111066
|
C | T | 5 | a0002c0005t0007g0057a0002c0079t0001g0095a0027c0034t0003g0166others(2): Show | 5 | HG02109.hp2 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-5873C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111066 | ||||||
| chr1:175111089
|
A | G | 149 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.2120-5850A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111089 | ||||||
| chr1:175111120
|
C | A | 1 | a0008c0007t0002g0133 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2120-5819C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111120 | ||||||
| chr1:175111233
|
G | A | 3 | a0004c0008t0001g0329a0004c0008t0002g0327a0004c0008t0002g0328 | 3 | NA19009.hp1 NA19056.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2120-5706G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111233 | ||||||
| chr1:175111345
|
GGCATGAT others(7): Show |
G | 5 | a0003c0002t0001g0297a0003c0002t0001g0299a0003c0002t0001g0321others(2): Show | 5 | HG02040.hp1 HG02523.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-5591_2120-557 others(18): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111345 | |||||
| chr1:175111425
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2120-5514C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111425 | ||||||
| chr1:175111426
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2120-5513G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111426 | ||||||
| chr1:175111486
|
C | CA | 7 | a0001c0016t0008g0045a0001c0028t0007g0044a0002c0079t0001g0095others(4): Show | 7 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2120-5423dupA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111486 | |||||
| chr1:175111486
|
CA | C | 106 | a0001c0016t0001g0356a0001c0016t0001g0358a0001c0016t0001g0359others(103): Show | 107 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.2120-5423delA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111486 | |||||
| chr1:175111486
|
CAA | C | 41 | a0001c0001t0001g0164a0001c0016t0001g0355a0001c0089t0001g0024others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.2120-5424_2120-542 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111486 | |||||
| chr1:175111486
|
CAAA | C | 122 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(119): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.2120-5425_2120-542 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111486 | |||||
| chr1:175111486
|
CAAAA | C | 35 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.2120-5426_2120-542 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111486 | |||||
| chr1:175111486
|
CAAAAAAA others(10): Show |
C | 11 | a0001c0016t0001g0040a0002c0009t0001g0036a0002c0009t0001g0037others(8): Show | 11 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2120-5439_2120-542 others(21): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111486 | |||||
| chr1:175111649
|
G | T | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-5290G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111649 | ||||||
| chr1:175111703
|
C | A | 1 | a0046c0091t0003g0104 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2120-5236C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111703 | ||||||
| chr1:175111778
|
A | AT | 23 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0123others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.2120-5150dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111778 | |||||
| chr1:175111778
|
AT | A | 62 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(59): Show | 62 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.2120-5150delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175111778 | |||||
| chr1:175111823
|
C | T | 1 | a0001c0016t0001g0358 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2120-5116C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111823 | ||||||
| chr1:175111854
|
A | G | 5 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-5085A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111854 | ||||||
| chr1:175111863
|
G | A | 11 | a0001c0042t0001g0059a0001c0042t0001g0097a0002c0005t0007g0057others(8): Show | 12 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2120-5076G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175111863 | ||||||
| chr1:175112246
|
TA | T | 14 | a0001c0001t0001g0344a0001c0001t0001g0352a0013c0014t0001g0056others(11): Show | 14 | HG01358.hp1 HG01891.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.2120-4692delA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112246 | ||||||
| chr1:175112304
|
T | C | 1 | a0003c0002t0001g0313 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2120-4635T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112304 | ||||||
| chr1:175112320
|
A | G | 5 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-4619A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112320 | ||||||
| chr1:175112485
|
T | C | 2 | a0004c0008t0002g0224a0004c0008t0002g0225 | 2 | NA18998.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2120-4454T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112485 | ||||||
| chr1:175112531
|
G | A | 12 | a0001c0016t0001g0040a0002c0009t0001g0036a0002c0009t0001g0037others(9): Show | 12 | HG01081.hp1 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2120-4408G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112531 | ||||||
| chr1:175112588
|
G | A | 2 | a0014c0024t0001g0161a0014c0024t0001g0162 | 2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2120-4351G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112588 | ||||||
| chr1:175112595
|
G | A | 5 | a0001c0016t0001g0356a0001c0016t0001g0358a0002c0009t0002g0361others(2): Show | 5 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-4344G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112595 | ||||||
| chr1:175112598
|
C | CT | 30 | a0004c0008t0001g0228a0004c0008t0002g0171a0004c0008t0002g0224others(27): Show | 30 | HG00280.hp2 HG00639.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2120-4304dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTT | 52 | a0003c0002t0001g0283a0003c0002t0001g0325a0003c0015t0001g0264others(49): Show | 52 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.2120-4305_2120-430 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTT | 73 | a0001c0001t0001g0352a0003c0002t0001g0266a0003c0002t0001g0270others(70): Show | 74 | HG00609.hp1 HG00609.hp2 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.2120-4306_2120-430 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTT | 37 | a0002c0005t0002g0342a0002c0029t0001g0055a0002c0029t0003g0053others(34): Show | 37 | HG00099.hp2 HG00544.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.2120-4307_2120-430 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTT | 16 | a0001c0001t0001g0338a0001c0016t0001g0356a0002c0009t0002g0363others(13): Show | 16 | HG01069.hp2 HG01168.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.2120-4308_2120-430 others(9): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTT | 21 | a0001c0001t0001g0107a0001c0001t0002g0122a0001c0031t0005g0156others(18): Show | 21 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2120-4309_2120-430 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT | 20 | a0001c0001t0001g0070a0001c0001t0001g0123a0001c0001t0001g0160others(17): Show | 21 | HG00140.hp1 HG00639.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.2120-4310_2120-430 others(11): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(1): Show |
9 | a0001c0001t0001g0128a0001c0001t0001g0151a0001c0001t0001g0331others(6): Show | 9 | HG00280.hp1 HG01106.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.2120-4311_2120-430 others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(2): Show |
8 | a0001c0016t0001g0359a0002c0005t0003g0103a0002c0005t0003g0106others(5): Show | 8 | HG01167.hp1 HG01192.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.2120-4312_2120-430 others(13): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0074a0001c0016t0001g0358a0001c0028t0001g0364others(3): Show | 6 | HG01261.hp2 HG01515.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.2120-4313_2120-430 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(4): Show |
7 | a0001c0001t0001g0158a0001c0001t0001g0323a0001c0083t0001g0159others(4): Show | 7 | HG00140.hp2 HG01192.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2120-4314_2120-430 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(5): Show |
10 | a0001c0001t0001g0031a0001c0001t0001g0108a0001c0001t0001g0324others(7): Show | 10 | HG01074.hp2 HG01109.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.2120-4315_2120-430 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0345a0001c0016t0001g0355a0014c0024t0001g0162others(1): Show | 4 | HG02615.hp2 HG03490.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.2120-4316_2120-430 others(17): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(8): Show |
3 | a0001c0001t0001g0018a0002c0037t0003g0360a0002c0037t0003g0366 | 3 | HG02559.hp2 HG02809.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.2120-4318_2120-430 others(19): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0020a0001c0001t0001g0023a0031c0068t0006g0100 | 3 | HG01943.hp1 HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2120-4319_2120-430 others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(13): Show |
1 | a0014c0024t0002g0021 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2120-4323_2120-430 others(24): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0001g0344a0013c0014t0001g0065 | 2 | HG04204.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2120-4324_2120-430 others(25): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0001g0333a0013c0014t0001g0060 | 2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2120-4326_2120-430 others(27): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2120-4327_2120-430 others(28): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(18): Show |
2 | a0001c0001t0001g0332a0022c0059t0001g0175 | 2 | HG01069.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2120-4328_2120-430 others(29): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0351 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2120-4329_2120-430 others(30): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(20): Show |
1 | a0001c0036t0001g0340 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2120-4330_2120-430 others(31): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(21): Show |
1 | a0039c0078t0003g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2120-4331_2120-430 others(32): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(22): Show |
1 | a0001c0036t0001g0341 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2120-4332_2120-430 others(33): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(23): Show |
1 | a0001c0031t0005g0330 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2120-4333_2120-430 others(34): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(24): Show |
1 | a0013c0014t0001g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2120-4334_2120-430 others(35): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(27): Show |
1 | a0013c0014t0001g0066 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2120-4337_2120-430 others(38): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
C | CTTTTTTT others(29): Show |
1 | a0013c0014t0001g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2120-4339_2120-430 others(40): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
CTTT | C | 7 | a0002c0009t0001g0037a0002c0009t0001g0038a0002c0009t0001g0042others(4): Show | 7 | HG02055.hp2 HG02922.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2120-4306_2120-430 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
CTTTTTTT others(3): Show |
C | 7 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(4): Show | 7 | HG02109.hp2 HG02622.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2120-4313_2120-430 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0001g0334a0001c0042t0001g0059a0002c0026t0001g0001others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2120-4314_2120-430 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
CTTTTTTT others(6): Show |
C | 1 | a0002c0009t0003g0357 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2120-4316_2120-430 others(17): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
CTTTTTTT others(8): Show |
C | 5 | a0001c0001t0001g0164a0007c0006t0001g0369a0007c0006t0001g0371others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-4318_2120-430 others(19): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
CTTTTTTT others(9): Show |
C | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2120-4319_2120-430 others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112598
|
CTTTTTTT others(10): Show |
C | 1 | a0003c0048t0001g0293 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2120-4320_2120-430 others(21): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112598 | |||||
| chr1:175112771
|
C | T | 3 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046 | 3 | HG02896.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2120-4168C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112771 | ||||||
| chr1:175112784
|
AT | A | 11 | a0001c0016t0001g0040a0002c0009t0001g0036a0002c0009t0001g0037others(8): Show | 11 | HG02055.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2120-4146delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175112784 | |||||
| chr1:175112917
|
C | T | 6 | a0001c0042t0001g0059a0001c0042t0001g0097a0002c0026t0001g0001others(3): Show | 7 | HG01070.hp2 HG01071.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2120-4022C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112917 | ||||||
| chr1:175112926
|
C | T | 14 | a0001c0016t0001g0355a0001c0016t0001g0356a0001c0016t0001g0358others(11): Show | 14 | HG01168.hp2 HG01261.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2120-4013C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112926 | ||||||
| chr1:175112978
|
T | C | 1 | a0029c0096t0001g0308 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2120-3961T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175112978 | ||||||
| chr1:175113168
|
C | T | 87 | a0003c0002t0001g0266a0003c0002t0001g0270a0003c0002t0001g0278others(84): Show | 88 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2120-3771C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113168 | ||||||
| chr1:175113245
|
G | A | 1 | a0003c0048t0001g0293 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2120-3694G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113245 | ||||||
| chr1:175113332
|
C | T | 1 | a0002c0005t0002g0342 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2120-3607C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113332 | ||||||
| chr1:175113367
|
C | G | 1 | a0006c0004t0002g0242 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2120-3572C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113367 | ||||||
| chr1:175113427
|
T | C | 6 | a0001c0074t0001g0052a0002c0029t0001g0055a0002c0029t0003g0053others(3): Show | 6 | HG01069.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2120-3512T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113427 | ||||||
| chr1:175113614
|
G | A | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2120-3325G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113614 | ||||||
| chr1:175113805
|
C | A | 1 | a0002c0009t0003g0362 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2120-3134C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113805 | ||||||
| chr1:175113832
|
G | C | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2120-3107G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113832 | ||||||
| chr1:175113840
|
C | A | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-3099C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113840 | ||||||
| chr1:175113909
|
G | A | 1 | a0052c0064t0001g0196 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2120-3030G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113909 | ||||||
| chr1:175113921
|
T | C | 5 | a0003c0002t0001g0283a0003c0002t0001g0317a0003c0002t0012g0277others(2): Show | 5 | HG02698.hp1 HG02735.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-3018T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175113921 | ||||||
| chr1:175114156
|
T | G | 60 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2120-2783T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114156 | ||||||
| chr1:175114275
|
G | A | 51 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(48): Show | 51 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.2120-2664G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114275 | ||||||
| chr1:175114584
|
T | C | 1 | a0002c0009t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2120-2355T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114584 | ||||||
| chr1:175114736
|
GGAA | G | 56 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(53): Show | 56 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.2120-2195_2120-219 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175114736 | |||||
| chr1:175114770
|
T | G | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-2169T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114770 | ||||||
| chr1:175114816
|
T | C | 60 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2120-2123T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114816 | ||||||
| chr1:175114874
|
A | G | 280 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(277): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.2120-2065A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114874 | ||||||
| chr1:175114886
|
G | A | 1 | a0003c0048t0001g0293 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2120-2053G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175114886 | ||||||
| chr1:175115247
|
A | G | 5 | a0008c0007t0001g0087a0008c0007t0002g0084a0008c0007t0002g0141others(2): Show | 5 | NA18962.hp1 NA18971.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-1692A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115247 | ||||||
| chr1:175115282
|
C | T | 1 | a0038c0069t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2120-1657C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115282 | ||||||
| chr1:175115332
|
AGG | A | 46 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(43): Show | 46 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.2120-1606_2120-160 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115332 | ||||||
| chr1:175115336
|
G | A | 46 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(43): Show | 46 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.2120-1603G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115336 | ||||||
| chr1:175115339
|
GA | G | 46 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(43): Show | 46 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.2120-1597delA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175115339 | |||||
| chr1:175115341
|
A | C | 46 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(43): Show | 46 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.2120-1598A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115341 | ||||||
| chr1:175115344
|
TAGTGC | T | 46 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(43): Show | 46 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.2120-1591_2120-158 others(9): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175115344 | |||||
| chr1:175115494
|
C | T | 6 | a0001c0042t0001g0059a0001c0042t0001g0097a0002c0026t0001g0001others(3): Show | 7 | HG01070.hp2 HG01071.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2120-1445C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115494 | ||||||
| chr1:175115613
|
G | A | 2 | a0002c0005t0007g0057a0002c0079t0001g0095 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2120-1326G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115613 | ||||||
| chr1:175115681
|
C | T | 2 | a0024c0039t0009g0010a0024c0039t0009g0012 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2120-1258C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115681 | ||||||
| chr1:175115688
|
G | A | 6 | a0001c0074t0001g0052a0002c0029t0001g0055a0002c0029t0003g0053others(3): Show | 6 | HG01069.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2120-1251G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115688 | ||||||
| chr1:175115699
|
A | G | 4 | a0001c0042t0001g0059a0002c0026t0001g0001a0002c0026t0003g0062others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-1240A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115699 | ||||||
| chr1:175115721
|
C | G | 54 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2120-1218C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115721 | ||||||
| chr1:175115769
|
C | T | 1 | a0018c0018t0001g0275 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2120-1170C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175115769 | ||||||
| chr1:175116046
|
A | AT | 6 | a0002c0005t0007g0057a0002c0079t0001g0095a0007c0073t0001g0051others(3): Show | 6 | HG02109.hp2 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2120-883dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175116046 | |||||
| chr1:175116084
|
T | C | 1 | a0001c0001t0001g0331 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2120-855T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175116084 | ||||||
| chr1:175116178
|
A | G | 3 | a0002c0005t0001g0119a0002c0005t0003g0149a0002c0005t0003g0150 | 3 | HG00140.hp1 HG02257.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2120-761A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175116178 | ||||||
| chr1:175116218
|
C | CT | 5 | a0002c0005t0007g0057a0002c0079t0001g0095a0027c0034t0003g0166others(2): Show | 5 | HG02109.hp2 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120-713dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175116218 | |||||
| chr1:175116235
|
G | A | 12 | a0001c0016t0001g0040a0002c0009t0001g0036a0002c0009t0001g0037others(9): Show | 12 | HG01081.hp1 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2120-704G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175116235 | ||||||
| chr1:175116439
|
G | GAAGTA | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2120-496_2120-492d others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 175116439 | |||||
| chr1:175116687
|
C | T | 1 | a0004c0019t0001g0209 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2120-252C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175116687 | ||||||
| chr1:175116693
|
T | C | 2 | a0001c0042t0001g0097a0036c0090t0005g0102 | 2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2120-246T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 9/18 | chr1 | 175116693 | ||||||
| chr1:175117325
|
A | G | 236 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(233): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2386+120A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175117325 | ||||||
| chr1:175117816
|
G | A | 1 | a0004c0019t0001g0353 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2386+611G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175117816 | ||||||
| chr1:175117829
|
T | G | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.2386+624T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175117829 | ||||||
| chr1:175117845
|
C | T | 1 | a0002c0005t0002g0019 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2386+640C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175117845 | ||||||
| chr1:175117900
|
T | G | 1 | a0005c0003t0001g0255 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2387-661T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175117900 | ||||||
| chr1:175118111
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2387-450C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175118111 | ||||||
| chr1:175118213
|
C | A | 1 | a0047c0045t0001g0207 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2387-348C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175118213 | ||||||
| chr1:175118470
|
T | C | 56 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(53): Show | 56 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.2387-91T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175118470 | ||||||
| chr1:175118484
|
C | T | 3 | a0033c0072t0004g0013a0034c0070t0004g0014a0035c0071t0004g0015 | 3 | HG02622.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2387-77C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175118484 | ||||||
| chr1:175118541
|
G | A | 154 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(151): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.2387-20G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | chr1 | 175118541 | ||||||
| chr1:175118547
|
A | AT | 61 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG01106.hp2 others(58): Show |
splice_region_variant&intron_variant | LOW | c.2387-4dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 175118547 | |||||
| chr1:175118933
|
A | G | 1 | a0008c0007t0002g0137 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2650+109A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175118933 | ||||||
| chr1:175118992
|
G | A | 1 | a0001c0016t0001g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2650+168G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175118992 | ||||||
| chr1:175119030
|
G | A | 1 | a0009c0021t0001g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2650+206G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119030 | ||||||
| chr1:175119051
|
G | A | 60 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2650+227G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119051 | ||||||
| chr1:175119172
|
C | T | 2 | a0004c0008t0002g0224a0004c0008t0002g0225 | 2 | NA18998.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2650+348C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119172 | ||||||
| chr1:175119309
|
A | G | 2 | a0013c0014t0001g0060a0013c0014t0001g0065 | 2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2650+485A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119309 | ||||||
| chr1:175119401
|
C | T | 60 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0107others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2650+577C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119401 | ||||||
| chr1:175119516
|
A | G | 90 | a0004c0008t0001g0173a0004c0008t0001g0228a0004c0008t0001g0329others(87): Show | 90 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.2650+692A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119516 | ||||||
| chr1:175119629
|
C | CTT | 26 | a0001c0001t0001g0331a0001c0016t0001g0356a0001c0016t0001g0358others(23): Show | 27 | HG01070.hp2 HG01071.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2650+812_2650+813d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175119629 | |||||
| chr1:175119629
|
C | CTTT | 69 | a0001c0016t0001g0355a0001c0074t0001g0052a0002c0009t0002g0363others(66): Show | 70 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.2650+811_2650+813d others(5): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175119629 | |||||
| chr1:175119629
|
C | CTTTT | 27 | a0002c0029t0003g0054a0003c0002t0001g0266a0003c0002t0001g0291others(24): Show | 27 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.2650+810_2650+813d others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175119629 | |||||
| chr1:175119637
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2650+813T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119637 | ||||||
| chr1:175119637
|
TC | T | 4 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2650+814delC | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119637 | ||||||
| chr1:175119638
|
C | CT | 14 | a0001c0016t0001g0040a0002c0009t0001g0036a0002c0009t0001g0037others(11): Show | 14 | HG00738.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2650+830dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175119638 | |||||
| chr1:175119638
|
C | T | 133 | a0001c0001t0001g0125a0001c0001t0001g0164a0001c0001t0001g0331others(130): Show | 135 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.2650+814C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119638 | ||||||
| chr1:175119650
|
T | C | 1 | a0008c0007t0002g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2650+826T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119650 | ||||||
| chr1:175119658
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2650+834A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119658 | ||||||
| chr1:175119720
|
C | T | 85 | a0003c0002t0001g0266a0003c0002t0001g0270a0003c0002t0001g0278others(82): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.2650+896C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119720 | ||||||
| chr1:175119727
|
C | T | 2 | a0001c0074t0001g0052a0007c0073t0001g0051 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2650+903C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119727 | ||||||
| chr1:175119779
|
C | T | 1 | a0010c0010t0001g0113 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2650+955C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119779 | ||||||
| chr1:175119783
|
C | T | 1 | a0038c0069t0002g0034 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2650+959C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119783 | ||||||
| chr1:175119791
|
T | C | 1 | a0007c0006t0001g0349 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2650+967T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119791 | ||||||
| chr1:175119795
|
C | T | 2 | a0010c0010t0001g0111a0010c0010t0001g0113 | 2 | HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.2650+971C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119795 | ||||||
| chr1:175119816
|
T | A | 2 | a0001c0074t0001g0052a0007c0073t0001g0051 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2650+992T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119816 | ||||||
| chr1:175119912
|
A | G | 98 | a0001c0016t0001g0355a0001c0016t0001g0359a0001c0028t0001g0364others(95): Show | 99 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.2650+1088A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119912 | ||||||
| chr1:175119929
|
C | T | 2 | a0001c0001t0001g0070a0001c0042t0001g0059 | 2 | HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2650+1105C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119929 | ||||||
| chr1:175119946
|
G | A | 49 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(46): Show | 49 | HG00099.hp2 HG01106.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.2650+1122G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119946 | ||||||
| chr1:175119958
|
T | C | 43 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(40): Show | 43 | HG00099.hp2 HG01106.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.2650+1134T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119958 | ||||||
| chr1:175119993
|
C | T | 5 | a0002c0005t0004g0008a0007c0006t0004g0009a0007c0006t0015g0011others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+1169C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175119993 | ||||||
| chr1:175120121
|
T | C | 8 | a0001c0001t0001g0158a0001c0042t0001g0097a0002c0026t0003g0062others(5): Show | 8 | HG02622.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2650+1297T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120121 | ||||||
| chr1:175120288
|
C | T | 2 | a0029c0096t0001g0308a0030c0095t0003g0307 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2650+1464C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120288 | ||||||
| chr1:175120307
|
T | C | 3 | a0001c0001t0001g0128a0001c0016t0001g0359a0002c0005t0001g0129 | 3 | HG03516.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2650+1483T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120307 | ||||||
| chr1:175120407
|
C | T | 1 | a0007c0038t0011g0368 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2650+1583C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120407 | ||||||
| chr1:175120411
|
C | G | 1 | a0004c0019t0001g0353 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2650+1587C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120411 | ||||||
| chr1:175120436
|
T | C | 11 | a0001c0016t0008g0045a0001c0028t0007g0044a0001c0028t0007g0046others(8): Show | 11 | HG01069.hp1 HG01192.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2650+1612T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120436 | ||||||
| chr1:175120475
|
C | T | 13 | a0001c0001t0001g0070a0001c0001t0001g0323a0001c0001t0001g0350others(10): Show | 13 | HG01192.hp1 HG01433.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.2650+1651C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120475 | ||||||
| chr1:175120520
|
G | A | 7 | a0002c0005t0001g0129a0023c0043t0001g0032a0023c0043t0001g0033others(4): Show | 7 | HG02451.hp1 HG02723.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2650+1696G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120520 | ||||||
| chr1:175120529
|
T | C | 2 | a0004c0008t0002g0206a0007c0006t0001g0094 | 2 | HG02523.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.2650+1705T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120529 | ||||||
| chr1:175120632
|
T | C | 4 | a0003c0002t0001g0305a0006c0004t0001g0191a0006c0004t0001g0213others(1): Show | 4 | HG00738.hp2 HG01123.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.2650+1808T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120632 | ||||||
| chr1:175120665
|
C | T | 1 | a0041c0085t0001g0088 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2650+1841C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120665 | ||||||
| chr1:175120738
|
TG | T | 49 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0031others(46): Show | 50 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.2650+1916delG | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175120738 | |||||
| chr1:175120827
|
G | T | 88 | a0002c0005t0002g0019a0003c0002t0001g0266a0003c0002t0001g0270others(85): Show | 88 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.2650+2003G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120827 | ||||||
| chr1:175120958
|
A | G | 203 | a0001c0016t0001g0356a0001c0016t0001g0358a0001c0031t0005g0075others(200): Show | 204 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.2650+2134A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175120958 | ||||||
| chr1:175121035
|
G | A | 1 | a0058c0094t0001g0227 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2650+2211G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121035 | ||||||
| chr1:175121278
|
A | G | 314 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.2651-2122A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121278 | ||||||
| chr1:175121290
|
T | C | 2 | a0022c0058t0006g0274a0022c0060t0006g0316 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2651-2110T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121290 | ||||||
| chr1:175121301
|
C | G | 311 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.2651-2099C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121301 | ||||||
| chr1:175121312
|
G | A | 4 | a0007c0006t0001g0337a0007c0006t0001g0369a0029c0096t0001g0308others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2651-2088G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121312 | ||||||
| chr1:175121418
|
C | T | 216 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.2651-1982C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121418 | ||||||
| chr1:175121499
|
T | G | 2 | a0007c0006t0001g0371a0007c0006t0015g0011 | 2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2651-1901T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121499 | ||||||
| chr1:175121592
|
G | A | 1 | a0003c0002t0001g0291 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2651-1808G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121592 | ||||||
| chr1:175121631
|
C | A | 212 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.2651-1769C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121631 | ||||||
| chr1:175121701
|
GGAT | G | 213 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2651-1695_2651-169 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175121701 | |||||
| chr1:175121803
|
T | C | 2 | a0029c0096t0001g0308a0030c0095t0003g0307 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2651-1597T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121803 | ||||||
| chr1:175121822
|
G | C | 116 | a0001c0036t0001g0341a0003c0002t0001g0266a0003c0002t0001g0270others(113): Show | 116 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.2651-1578G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121822 | ||||||
| chr1:175121844
|
G | A | 213 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2651-1556G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121844 | ||||||
| chr1:175121958
|
A | C | 1 | a0002c0005t0001g0119 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2651-1442A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175121958 | ||||||
| chr1:175122015
|
G | A | 85 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(82): Show | 86 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2651-1385G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122015 | ||||||
| chr1:175122201
|
G | T | 1 | a0043c0086t0001g0076 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2651-1199G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122201 | ||||||
| chr1:175122218
|
C | CAA | 213 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(210): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2651-1171_2651-117 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175122218 | |||||
| chr1:175122218
|
C | CAAA | 9 | a0001c0001t0001g0331a0001c0001t0001g0334a0001c0031t0005g0075others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2651-1172_2651-117 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175122218 | |||||
| chr1:175122417
|
C | T | 4 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(1): Show | 4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2651-983C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122417 | ||||||
| chr1:175122455
|
TTGCTAAC others(45): Show |
T | 213 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2651-942_2651-891d others(54): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 175122455 | |||||
| chr1:175122510
|
T | A | 213 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2651-890T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122510 | ||||||
| chr1:175122518
|
G | A | 9 | a0001c0001t0001g0331a0001c0028t0001g0364a0001c0028t0007g0044others(6): Show | 9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2651-882G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122518 | ||||||
| chr1:175122579
|
C | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0333others(1): Show | 4 | HG02896.hp2 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2651-821C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122579 | ||||||
| chr1:175122847
|
T | A | 85 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(82): Show | 86 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2651-553T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122847 | ||||||
| chr1:175122847
|
T | C | 9 | a0001c0001t0001g0331a0001c0028t0001g0364a0001c0028t0007g0044others(6): Show | 9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2651-553T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122847 | ||||||
| chr1:175122909
|
A | C | 2 | a0037c0080t0001g0165a0044c0087t0001g0335 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2651-491A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122909 | ||||||
| chr1:175122997
|
C | A | 84 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(81): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.2651-403C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175122997 | ||||||
| chr1:175123000
|
C | G | 120 | a0003c0002t0001g0266a0003c0002t0001g0270a0003c0002t0001g0278others(117): Show | 120 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.2651-400C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175123000 | ||||||
| chr1:175123014
|
G | A | 9 | a0001c0001t0001g0331a0001c0028t0001g0364a0001c0028t0007g0044others(6): Show | 9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2651-386G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175123014 | ||||||
| chr1:175123226
|
T | C | 1 | a0002c0005t0003g0103 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2651-174T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 11/18 | chr1 | 175123226 | ||||||
| chr1:175123686
|
G | A | 1 | a0012c0013t0001g0101 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2914+23G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175123686 | ||||||
| chr1:175123704
|
T | C | 214 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2914+41T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175123704 | ||||||
| chr1:175123767
|
C | T | 3 | a0002c0009t0003g0365a0002c0037t0003g0360a0002c0037t0003g0366 | 3 | HG02559.hp2 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2914+104C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175123767 | ||||||
| chr1:175123781
|
A | G | 1 | a0001c0031t0005g0330 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2914+118A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175123781 | ||||||
| chr1:175123856
|
GGAGT | G | 289 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.2914+199_2914+202d others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175123856 | |||||
| chr1:175123887
|
C | T | 1 | a0020c0022t0001g0298 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2914+224C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175123887 | ||||||
| chr1:175123954
|
A | G | 2 | a0008c0007t0002g0071a0008c0007t0002g0072 | 2 | NA18948.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2914+291A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175123954 | ||||||
| chr1:175124235
|
G | T | 213 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2914+572G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124235 | ||||||
| chr1:175124407
|
G | A | 4 | a0023c0043t0001g0032a0023c0043t0001g0033a0024c0039t0009g0010others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2914+744G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124407 | ||||||
| chr1:175124408
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2914+745C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124408 | ||||||
| chr1:175124447
|
A | G | 226 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(223): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.2914+784A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124447 | ||||||
| chr1:175124632
|
G | T | 119 | a0003c0002t0001g0266a0003c0002t0001g0270a0003c0002t0001g0278others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2914+969G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124632 | ||||||
| chr1:175124687
|
GCAAA | G | 75 | a0002c0005t0004g0008a0002c0005t0007g0057a0002c0009t0001g0036others(72): Show | 76 | HG00639.hp1 HG01070.hp1 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.2914+1050_2914+105 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175124687 | |||||
| chr1:175124687
|
GCAAACAA others(1): Show |
G | 213 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2914+1046_2914+105 others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175124687 | |||||
| chr1:175124731
|
T | C | 311 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.2914+1068T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124731 | ||||||
| chr1:175124889
|
G | A | 85 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(82): Show | 86 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2914+1226G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175124889 | ||||||
| chr1:175125363
|
T | TA | 63 | a0002c0005t0007g0057a0002c0026t0003g0062a0002c0026t0003g0063others(60): Show | 63 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.2915-1581dupA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125363 | |||||
| chr1:175125461
|
TC | T | 3 | a0002c0026t0003g0062a0002c0026t0003g0063a0031c0068t0006g0100 | 3 | HG01943.hp1 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2915-1491delC | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125461 | |||||
| chr1:175125516
|
ATCCCTTC others(4): Show |
A | 2 | a0005c0003t0001g0169a0005c0003t0001g0181 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2915-1433_2915-142 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125516 | |||||
| chr1:175125517
|
T | A | 1 | a0005c0003t0001g0258 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2915-1438T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125517 | ||||||
| chr1:175125586
|
CCTCTTTC others(3): Show |
C | 1 | a0001c0001t0001g0350 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2915-1356_2915-134 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125586 | |||||
| chr1:175125666
|
TCTCC | T | 62 | a0002c0005t0007g0057a0002c0026t0003g0062a0002c0026t0003g0063others(59): Show | 62 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.2915-1276_2915-127 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125666 | |||||
| chr1:175125670
|
C | T | 1 | a0004c0019t0002g0237 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2915-1285C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125670 | ||||||
| chr1:175125684
|
T | C | 214 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2915-1271T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125684 | ||||||
| chr1:175125685
|
T | C | 1 | a0008c0007t0002g0137 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2915-1270T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125685 | ||||||
| chr1:175125697
|
TTTTCTCT others(5): Show |
T | 1 | a0008c0007t0002g0132 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2915-1252_2915-124 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125697 | |||||
| chr1:175125699
|
TTC | T | 43 | a0001c0001t0001g0023a0001c0001t0001g0323a0001c0001t0001g0333others(40): Show | 43 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2915-1250_2915-124 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125699 | |||||
| chr1:175125701
|
CTCTCTT | C | 39 | a0001c0001t0001g0031a0001c0001t0001g0107a0001c0001t0001g0108others(36): Show | 39 | HG00408.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.2915-1250_2915-124 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125701 | |||||
| chr1:175125701
|
CTCTCTTT others(3): Show |
C | 68 | a0001c0001t0001g0020a0001c0001t0001g0070a0001c0001t0001g0074others(65): Show | 69 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.2915-1250_2915-124 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125701 | |||||
| chr1:175125701
|
CTCTCTTT others(7): Show |
C | 18 | a0001c0001t0001g0160a0001c0001t0001g0350a0001c0016t0001g0040others(15): Show | 18 | HG00408.hp2 HG00738.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2915-1250_2915-123 others(18): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125701 | |||||
| chr1:175125701
|
CTCTCTTT others(11): Show |
C | 11 | a0001c0001t0001g0164a0001c0001t0001g0351a0001c0016t0001g0358others(8): Show | 11 | HG00642.hp2 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2915-1250_2915-123 others(22): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125701 | |||||
| chr1:175125701
|
CTCTCTTT others(15): Show |
C | 5 | a0013c0014t0001g0056a0023c0043t0001g0032a0023c0043t0001g0033others(2): Show | 5 | HG01358.hp1 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2915-1250_2915-122 others(26): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125701 | |||||
| chr1:175125701
|
CTCTCTTT others(27): Show |
C | 1 | a0006c0063t0002g0217 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2915-1250_2915-121 others(38): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125701 | |||||
| chr1:175125703
|
C | CTCTTTCT others(5): Show |
1 | a0008c0040t0003g0145 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2915-1208_2915-119 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | |||||
| chr1:175125703
|
C | CTT | 22 | a0001c0001t0001g0018a0001c0001t0001g0151a0001c0001t0001g0158others(19): Show | 22 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.2915-1251_2915-125 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | |||||
| chr1:175125703
|
C | CTTTCTT | 5 | a0001c0001t0001g0346a0001c0016t0001g0356a0003c0015t0001g0312others(2): Show | 5 | HG01255.hp1 HG01517.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2915-1251_2915-125 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | |||||
| chr1:175125703
|
C | CTTTCTTT others(3): Show |
1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2915-1251_2915-125 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | |||||
| chr1:175125703
|
CTCTT | C | 27 | a0002c0005t0016g0030a0004c0008t0002g0208a0004c0008t0002g0226others(24): Show | 28 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.2915-1200_2915-119 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | |||||
| chr1:175125703
|
CTCTTTCT others(1): Show |
C | 38 | a0002c0005t0002g0116a0002c0005t0002g0347a0002c0005t0004g0008others(35): Show | 38 | HG00642.hp1 HG01081.hp1 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.2915-1204_2915-119 others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | |||||
| chr1:175125703
|
CTCTTTCT others(5): Show |
C | 23 | a0002c0005t0001g0119a0002c0005t0001g0121a0002c0005t0002g0019others(20): Show | 24 | HG00140.hp1 HG00323.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.2915-1208_2915-119 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | |||||
| chr1:175125703
|
CTCTTTCT others(9): Show |
C | 20 | a0002c0005t0002g0022a0002c0005t0007g0057a0002c0009t0001g0036others(17): Show | 20 | HG01243.hp1 HG01256.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.2915-1212_2915-119 others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | |||||
| chr1:175125703
|
CTCTTTCT others(13): Show |
C | 5 | a0002c0009t0001g0049a0004c0056t0002g0193a0017c0025t0001g0093others(2): Show | 5 | HG02129.hp2 NA18906.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.2915-1216_2915-119 others(24): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | |||||
| chr1:175125703
|
CTCTTTCT others(25): Show |
C | 22 | a0002c0005t0001g0129a0002c0005t0003g0103a0002c0005t0003g0105others(19): Show | 22 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.2915-1228_2915-119 others(36): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | |||||
| chr1:175125703
|
CTCTTTCT others(37): Show |
C | 1 | a0035c0071t0004g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2915-1240_2915-119 others(48): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125703 | |||||
| chr1:175125745
|
CTTTCTTT others(3): Show |
C | 1 | a0011c0011t0001g0240 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2915-1208_2915-119 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125745 | |||||
| chr1:175125753
|
CTT | C | 4 | a0007c0006t0001g0337a0007c0006t0001g0369a0029c0096t0001g0308others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2915-1200_2915-119 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125753 | |||||
| chr1:175125755
|
T | C | 1 | a0007c0006t0001g0371 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2915-1200T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125755 | ||||||
| chr1:175125759
|
C | T | 1 | a0012c0013t0001g0073 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2915-1196C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125759 | ||||||
| chr1:175125811
|
C | T | 289 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.2915-1144C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125811 | ||||||
| chr1:175125818
|
CCTCCTTT others(18): Show |
C | 1 | a0042c0084t0001g0079 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2915-1136_2915-111 others(29): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125818 | ||||||
| chr1:175125822
|
CTTTCTTT others(14): Show |
C | 301 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(298): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.2915-1095_2915-107 others(25): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125822 | |||||
| chr1:175125823
|
T | C | 13 | a0002c0005t0004g0008a0002c0009t0001g0036a0002c0009t0001g0037others(10): Show | 14 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2915-1132T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125823 | ||||||
| chr1:175125825
|
T | C | 13 | a0002c0005t0004g0008a0002c0009t0001g0036a0002c0009t0001g0037others(10): Show | 14 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2915-1130T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125825 | ||||||
| chr1:175125826
|
CTTTCTTT others(10): Show |
C | 13 | a0002c0005t0004g0008a0002c0009t0001g0036a0002c0009t0001g0037others(10): Show | 14 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2915-1117_2915-110 others(21): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125826 | |||||
| chr1:175125844
|
T | C | 63 | a0002c0005t0007g0057a0002c0026t0003g0062a0002c0026t0003g0063others(60): Show | 63 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.2915-1111T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125844 | ||||||
| chr1:175125846
|
T | C | 63 | a0002c0005t0007g0057a0002c0026t0003g0062a0002c0026t0003g0063others(60): Show | 63 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.2915-1109T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125846 | ||||||
| chr1:175125893
|
C | A | 1 | a0036c0090t0005g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2915-1062C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175125893 | ||||||
| chr1:175125963
|
T | TTC | 174 | a0002c0005t0007g0057a0002c0026t0003g0062a0002c0026t0003g0063others(171): Show | 174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2915-973_2915-972d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125963 | |||||
| chr1:175125963
|
TTCTC | T | 3 | a0001c0001t0001g0334a0001c0042t0001g0059a0019c0023t0001g0241 | 3 | HG02486.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2915-975_2915-972d others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175125963 | |||||
| chr1:175126057
|
A | C | 1 | a0002c0005t0002g0019 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2915-898A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126057 | ||||||
| chr1:175126077
|
G | A | 1 | a0003c0002t0001g0266 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2915-878G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126077 | ||||||
| chr1:175126104
|
C | CT | 164 | a0002c0005t0007g0057a0002c0026t0003g0062a0002c0026t0003g0063others(161): Show | 164 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.2915-836dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175126104 | |||||
| chr1:175126104
|
C | CTT | 15 | a0001c0001t0001g0333a0001c0001t0001g0346a0001c0016t0001g0356others(12): Show | 15 | HG01255.hp1 HG01517.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2915-837_2915-836d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175126104 | |||||
| chr1:175126104
|
C | CTTT | 100 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(97): Show | 102 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.2915-838_2915-836d others(5): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175126104 | |||||
| chr1:175126104
|
C | CTTTT | 6 | a0001c0031t0005g0075a0007c0006t0001g0337a0007c0006t0001g0369others(3): Show | 6 | HG02280.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2915-839_2915-836d others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 175126104 | |||||
| chr1:175126161
|
A | G | 124 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(121): Show | 126 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2915-794A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126161 | ||||||
| chr1:175126258
|
T | C | 287 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(284): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.2915-697T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126258 | ||||||
| chr1:175126327
|
C | A | 120 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(117): Show | 122 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2915-628C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126327 | ||||||
| chr1:175126347
|
G | A | 3 | a0001c0031t0005g0075a0001c0031t0005g0156a0001c0031t0005g0330 | 3 | HG01884.hp1 HG03471.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2915-608G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126347 | ||||||
| chr1:175126397
|
G | A | 1 | a0001c0042t0001g0097 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2915-558G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126397 | ||||||
| chr1:175126438
|
G | A | 24 | a0002c0005t0001g0129a0002c0005t0003g0103a0002c0005t0003g0105others(21): Show | 24 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.2915-517G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126438 | ||||||
| chr1:175126440
|
C | T | 119 | a0002c0005t0002g0019a0002c0005t0002g0022a0003c0002t0001g0266others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2915-515C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126440 | ||||||
| chr1:175126513
|
T | C | 1 | a0036c0090t0005g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2915-442T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126513 | ||||||
| chr1:175126729
|
G | A | 2 | a0023c0043t0001g0032a0023c0043t0001g0033 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2915-226G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126729 | ||||||
| chr1:175126800
|
C | T | 94 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(91): Show | 95 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.2915-155C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126800 | ||||||
| chr1:175126884
|
C | T | 3 | a0007c0006t0001g0061a0022c0059t0001g0175a0033c0072t0004g0013 | 3 | HG01069.hp1 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2915-71C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126884 | ||||||
| chr1:175126885
|
T | C | 3 | a0001c0001t0001g0334a0001c0042t0001g0059a0019c0023t0001g0241 | 3 | HG02486.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2915-70T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126885 | ||||||
| chr1:175126918
|
T | A | 2 | a0037c0080t0001g0165a0044c0087t0001g0335 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2915-37T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 12/18 | chr1 | 175126918 | ||||||
| chr1:175127089
|
C | T | 1 | a0011c0011t0001g0238 | 1 | HG00408.hp1 | splice_region_variant&intron_variant | LOW | c.3045+4C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127089 | ||||||
| chr1:175127128
|
G | A | 1 | a0013c0014t0001g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3045+43G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127128 | ||||||
| chr1:175127176
|
G | T | 2 | a0007c0006t0001g0371a0007c0006t0015g0011 | 2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3045+91G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127176 | ||||||
| chr1:175127197
|
A | G | 178 | a0001c0001t0001g0331a0001c0016t0008g0045a0001c0031t0005g0075others(175): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.3045+112A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127197 | ||||||
| chr1:175127197
|
A | T | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3045+112A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127197 | ||||||
| chr1:175127242
|
G | T | 1 | a0004c0032t0002g0192 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3045+157G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127242 | ||||||
| chr1:175127253
|
C | T | 177 | a0001c0001t0001g0331a0001c0016t0008g0045a0001c0031t0005g0075others(174): Show | 177 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.3045+168C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127253 | ||||||
| chr1:175127254
|
C | T | 3 | a0001c0016t0001g0359a0015c0092t0001g0124a0042c0084t0001g0079 | 3 | HG00642.hp2 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3045+169C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127254 | ||||||
| chr1:175127437
|
A | G | 1 | a0003c0002t0001g0313 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3045+352A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127437 | ||||||
| chr1:175127589
|
G | A | 98 | a0001c0001t0001g0331a0002c0005t0007g0057a0002c0009t0001g0049others(95): Show | 98 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.3046-443G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127589 | ||||||
| chr1:175127680
|
G | A | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3046-352G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127680 | ||||||
| chr1:175127774
|
G | A | 65 | a0003c0015t0001g0264a0003c0015t0001g0312a0003c0015t0003g0261others(62): Show | 65 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(62): Show |
intron_variant | MODIFIER | c.3046-258G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127774 | ||||||
| chr1:175127879
|
C | T | 2 | a0001c0001t0001g0074a0001c0082t0008g0131 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3046-153C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127879 | ||||||
| chr1:175127958
|
C | T | 27 | a0002c0005t0001g0129a0002c0005t0003g0103a0002c0005t0003g0105others(24): Show | 27 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.3046-74C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175127958 | ||||||
| chr1:175128023
|
G | A | 3 | a0007c0006t0001g0337a0007c0006t0001g0369a0029c0096t0001g0308 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3046-9G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 13/18 | chr1 | 175128023 | ||||||
| chr1:175128195
|
G | A | 141 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(138): Show | 142 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.3178+31G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128195 | ||||||
| chr1:175128213
|
C | T | 235 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.3178+49C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128213 | ||||||
| chr1:175128221
|
C | G | 103 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(100): Show | 103 | HG00639.hp1 HG01070.hp1 HG01109.hp2 others(100): Show |
intron_variant | MODIFIER | c.3178+57C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128221 | ||||||
| chr1:175128263
|
A | T | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3178+99A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128263 | ||||||
| chr1:175128277
|
G | A | 3 | a0002c0026t0003g0062a0002c0026t0003g0063a0031c0068t0006g0100 | 3 | HG01943.hp1 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3178+113G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128277 | ||||||
| chr1:175128361
|
G | C | 2 | a0022c0058t0006g0274a0022c0060t0006g0316 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3178+197G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128361 | ||||||
| chr1:175128411
|
C | A | 2 | a0002c0005t0001g0121a0008c0007t0002g0099 | 2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.3179-184C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128411 | ||||||
| chr1:175128533
|
G | A | 3 | a0004c0008t0002g0226a0004c0008t0002g0229a0009c0012t0002g0319 | 3 | NA18993.hp2 NA18995.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3179-62G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128533 | ||||||
| chr1:175128574
|
C | G | 1 | a0009c0021t0001g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3179-21C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 14/18 | chr1 | 175128574 | ||||||
| chr1:175128775
|
T | A | 26 | a0002c0005t0001g0129a0002c0005t0003g0103a0002c0005t0003g0105others(23): Show | 26 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.3330+29T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128775 | ||||||
| chr1:175128808
|
G | A | 11 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(8): Show | 11 | HG01192.hp2 HG02145.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.3330+62G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128808 | ||||||
| chr1:175128854
|
C | A | 1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3330+108C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128854 | ||||||
| chr1:175128855
|
C | T | 171 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(168): Show | 172 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.3330+109C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128855 | ||||||
| chr1:175128856
|
C | T | 1 | a0009c0021t0001g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3330+110C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128856 | ||||||
| chr1:175128900
|
G | A | 6 | a0003c0002t0001g0300a0003c0002t0001g0303a0006c0004t0001g0253others(3): Show | 6 | HG00438.hp2 HG00609.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.3330+154G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128900 | ||||||
| chr1:175128911
|
T | G | 34 | a0002c0005t0001g0129a0002c0005t0003g0103a0002c0005t0003g0105others(31): Show | 34 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.3330+165T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175128911 | ||||||
| chr1:175129023
|
A | G | 2 | a0036c0090t0005g0102a0051c0066t0010g0167 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3330+277A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175129023 | ||||||
| chr1:175129064
|
G | A | 7 | a0002c0009t0001g0036a0002c0009t0001g0037a0002c0009t0001g0039others(4): Show | 7 | HG02257.hp2 HG02630.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.3330+318G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175129064 | ||||||
| chr1:175129159
|
A | G | 1 | a0004c0032t0002g0192 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3330+413A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175129159 | ||||||
| chr1:175129318
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3330+572C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175129318 | ||||||
| chr1:175129400
|
C | T | 5 | a0001c0001t0001g0331a0002c0005t0007g0057a0002c0009t0001g0049others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.3330+654C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175129400 | ||||||
| chr1:175129609
|
C | T | 3 | a0007c0006t0001g0337a0007c0006t0001g0369a0029c0096t0001g0308 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3330+863C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175129609 | ||||||
| chr1:175130140
|
A | G | 1 | a0001c0016t0001g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3330+1394A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130140 | ||||||
| chr1:175130153
|
G | A | 1 | a0039c0078t0003g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3330+1407G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130153 | ||||||
| chr1:175130194
|
G | A | 4 | a0023c0043t0001g0032a0023c0043t0001g0033a0024c0039t0009g0010others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3330+1448G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130194 | ||||||
| chr1:175130234
|
A | C | 1 | a0007c0006t0001g0349 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3330+1488A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130234 | ||||||
| chr1:175130386
|
C | T | 1 | a0002c0009t0003g0362 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3330+1640C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130386 | ||||||
| chr1:175130438
|
C | T | 162 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(159): Show | 163 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.3330+1692C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130438 | ||||||
| chr1:175130564
|
C | T | 15 | a0001c0001t0001g0108a0001c0001t0001g0164a0001c0001t0001g0323others(12): Show | 15 | HG00639.hp2 HG01074.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.3330+1818C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130564 | ||||||
| chr1:175130610
|
CAGA | C | 93 | a0003c0002t0001g0266a0003c0002t0001g0270a0003c0002t0001g0278others(90): Show | 93 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.3330+1867_3330+186 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175130610 | |||||
| chr1:175130636
|
T | C | 200 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(197): Show | 201 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.3330+1890T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130636 | ||||||
| chr1:175130777
|
C | G | 25 | a0002c0005t0001g0129a0002c0005t0003g0103a0002c0005t0003g0105others(22): Show | 25 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.3330+2031C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130777 | ||||||
| chr1:175130780
|
A | G | 1 | a0027c0034t0003g0168 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3330+2034A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130780 | ||||||
| chr1:175130918
|
G | C | 2 | a0007c0006t0001g0371a0007c0006t0015g0011 | 2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3330+2172G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175130918 | ||||||
| chr1:175131038
|
GT | G | 8 | a0022c0058t0006g0274a0022c0060t0006g0316a0023c0043t0001g0032others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3330+2299delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131038 | |||||
| chr1:175131172
|
T | C | 2 | a0036c0090t0005g0102a0051c0066t0010g0167 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3330+2426T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175131172 | ||||||
| chr1:175131440
|
G | T | 2 | a0002c0029t0003g0053a0002c0029t0003g0054 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3330+2694G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175131440 | ||||||
| chr1:175131446
|
C | T | 198 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(195): Show | 199 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.3330+2700C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175131446 | ||||||
| chr1:175131587
|
C | CCTGTGGG others(6): Show |
1 | a0004c0019t0001g0200 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3330+2843_3330+285 others(17): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131587 | |||||
| chr1:175131727
|
C | G | 1 | a0007c0006t0001g0337 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3330+2981C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175131727 | ||||||
| chr1:175131917
|
T | TAC | 28 | a0001c0001t0001g0345a0001c0031t0005g0156a0002c0005t0002g0019others(25): Show | 28 | HG00099.hp2 HG00408.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.3330+3209_3330+321 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | |||||
| chr1:175131917
|
T | TACAC | 25 | a0001c0001t0001g0108a0001c0001t0001g0351a0001c0016t0001g0358others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.3330+3207_3330+321 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | |||||
| chr1:175131917
|
T | TACACAC | 58 | a0001c0001t0001g0031a0001c0001t0001g0107a0001c0001t0001g0158others(55): Show | 59 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.3330+3205_3330+321 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | |||||
| chr1:175131917
|
T | TACACACA others(1): Show |
44 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(41): Show | 44 | HG01070.hp1 HG01081.hp2 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.3330+3203_3330+321 others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | |||||
| chr1:175131917
|
T | TACACACA others(3): Show |
49 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0332others(46): Show | 49 | HG00639.hp1 HG01243.hp1 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.3330+3201_3330+321 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | |||||
| chr1:175131917
|
T | TACACACA others(5): Show |
14 | a0001c0074t0001g0052a0002c0026t0003g0062a0002c0026t0003g0063others(11): Show | 14 | HG01515.hp1 HG01517.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.3330+3199_3330+321 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | |||||
| chr1:175131917
|
T | TACACACA others(7): Show |
11 | a0002c0005t0003g0103a0002c0005t0003g0105a0002c0005t0003g0106others(8): Show | 11 | HG01192.hp1 HG01255.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.3330+3197_3330+321 others(18): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | |||||
| chr1:175131917
|
T | TACACACA others(9): Show |
2 | a0005c0003t0003g0256a0030c0095t0003g0307 | 2 | HG01934.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3330+3195_3330+321 others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | |||||
| chr1:175131917
|
T | TACACACA others(11): Show |
1 | a0018c0018t0001g0320 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3330+3193_3330+321 others(22): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | |||||
| chr1:175131917
|
TAC | T | 5 | a0002c0005t0002g0342a0003c0002t0001g0315a0009c0012t0003g0273others(2): Show | 5 | HG01109.hp2 HG02135.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.3330+3209_3330+321 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | |||||
| chr1:175131917
|
TACACAC | T | 6 | a0007c0006t0001g0006a0007c0006t0001g0007a0007c0006t0004g0009others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3330+3205_3330+321 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175131917 | |||||
| chr1:175131957
|
T | C | 2 | a0001c0031t0005g0156a0001c0031t0005g0330 | 2 | HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3330+3211T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175131957 | ||||||
| chr1:175132039
|
G | T | 5 | a0007c0006t0001g0006a0007c0006t0001g0007a0007c0006t0004g0009others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.3330+3293G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132039 | ||||||
| chr1:175132079
|
C | T | 103 | a0001c0001t0001g0331a0001c0028t0001g0364a0001c0028t0007g0044others(100): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.3330+3333C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132079 | ||||||
| chr1:175132090
|
A | G | 200 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(197): Show | 201 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.3330+3344A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132090 | ||||||
| chr1:175132098
|
T | C | 200 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(197): Show | 201 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.3330+3352T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132098 | ||||||
| chr1:175132308
|
A | G | 2 | a0036c0090t0005g0102a0051c0066t0010g0167 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3331-3537A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132308 | ||||||
| chr1:175132500
|
A | C | 9 | a0001c0001t0001g0070a0001c0001t0001g0128a0001c0001t0001g0332others(6): Show | 9 | HG02486.hp1 HG02572.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.3331-3345A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132500 | ||||||
| chr1:175132555
|
C | T | 1 | a0007c0038t0011g0368 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3331-3290C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132555 | ||||||
| chr1:175132897
|
C | T | 1 | a0021c0027t0001g0198 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3331-2948C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132897 | ||||||
| chr1:175132899
|
G | C | 1 | a0016c0020t0001g0147 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3331-2946G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175132899 | ||||||
| chr1:175133025
|
G | A | 110 | a0001c0001t0001g0331a0002c0005t0007g0057a0002c0009t0001g0049others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.3331-2820G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133025 | ||||||
| chr1:175133050
|
G | A | 5 | a0002c0005t0004g0008a0002c0009t0001g0038a0002c0009t0001g0047others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.3331-2795G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133050 | ||||||
| chr1:175133102
|
A | G | 306 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.3331-2743A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133102 | ||||||
| chr1:175133258
|
T | G | 2 | a0036c0090t0005g0102a0051c0066t0010g0167 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3331-2587T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133258 | ||||||
| chr1:175133273
|
T | A | 306 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.3331-2572T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133273 | ||||||
| chr1:175133603
|
C | T | 1 | a0002c0009t0001g0049 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3331-2242C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133603 | ||||||
| chr1:175133645
|
C | T | 3 | a0001c0016t0001g0356a0013c0014t0001g0056a0013c0014t0001g0069 | 3 | HG01358.hp1 HG01517.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3331-2200C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133645 | ||||||
| chr1:175133677
|
G | A | 4 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(1): Show | 4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-2168G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133677 | ||||||
| chr1:175133770
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3331-2075C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133770 | ||||||
| chr1:175133869
|
G | T | 306 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.3331-1976G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133869 | ||||||
| chr1:175133915
|
T | C | 4 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(1): Show | 4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-1930T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133915 | ||||||
| chr1:175133971
|
C | T | 2 | a0022c0058t0006g0274a0022c0060t0006g0316 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3331-1874C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175133971 | ||||||
| chr1:175134081
|
A | G | 308 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.3331-1764A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134081 | ||||||
| chr1:175134416
|
G | T | 1 | a0036c0090t0005g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3331-1429G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134416 | ||||||
| chr1:175134438
|
G | C | 196 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(193): Show | 197 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.3331-1407G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134438 | ||||||
| chr1:175134469
|
C | T | 1 | a0004c0008t0001g0228 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3331-1376C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134469 | ||||||
| chr1:175134475
|
G | A | 196 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(193): Show | 197 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.3331-1370G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134475 | ||||||
| chr1:175134544
|
C | CAA | 190 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(187): Show | 191 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.3331-1296_3331-129 others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175134544 | |||||
| chr1:175134544
|
C | CAAA | 6 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(3): Show | 6 | HG01192.hp2 HG02622.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3331-1297_3331-129 others(7): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175134544 | |||||
| chr1:175134551
|
C | A | 196 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(193): Show | 197 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.3331-1294C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134551 | ||||||
| chr1:175134852
|
CT | C | 110 | a0001c0001t0001g0331a0002c0005t0007g0057a0002c0009t0001g0049others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.3331-992delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134852 | ||||||
| chr1:175134854
|
G | A | 3 | a0006c0004t0001g0194a0006c0004t0001g0195a0056c0052t0001g0282 | 3 | HG02129.hp1 HG02165.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3331-991G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134854 | ||||||
| chr1:175134914
|
T | C | 2 | a0036c0090t0005g0102a0051c0066t0010g0167 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3331-931T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134914 | ||||||
| chr1:175134945
|
A | T | 4 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(1): Show | 4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-900A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134945 | ||||||
| chr1:175134987
|
A | AGGACTGA others(5): Show |
1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3331-856_3331-845d others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 175134987 | |||||
| chr1:175134987
|
A | G | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3331-858A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134987 | ||||||
| chr1:175134991
|
C | G | 2 | a0022c0058t0006g0274a0022c0060t0006g0316 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3331-854C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175134991 | ||||||
| chr1:175135064
|
G | A | 4 | a0007c0006t0001g0371a0007c0006t0015g0011a0036c0090t0005g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-781G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135064 | ||||||
| chr1:175135091
|
T | C | 4 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(1): Show | 4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-754T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135091 | ||||||
| chr1:175135117
|
G | T | 2 | a0036c0090t0005g0102a0051c0066t0010g0167 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3331-728G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135117 | ||||||
| chr1:175135132
|
C | T | 1 | a0011c0011t0001g0240 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3331-713C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135132 | ||||||
| chr1:175135384
|
AT | A | 4 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(1): Show | 4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-460delT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135384 | ||||||
| chr1:175135395
|
A | G | 1 | a0008c0007t0002g0071 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3331-450A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135395 | ||||||
| chr1:175135482
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3331-363A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135482 | ||||||
| chr1:175135538
|
T | C | 25 | a0002c0005t0001g0129a0002c0005t0003g0103a0002c0005t0003g0105others(22): Show | 25 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.3331-307T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135538 | ||||||
| chr1:175135557
|
C | G | 25 | a0002c0005t0001g0129a0002c0005t0003g0103a0002c0005t0003g0105others(22): Show | 25 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.3331-288C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135557 | ||||||
| chr1:175135583
|
T | C | 208 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.3331-262T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135583 | ||||||
| chr1:175135654
|
T | C | 99 | a0001c0001t0001g0331a0002c0005t0007g0057a0002c0009t0001g0049others(96): Show | 99 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.3331-191T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135654 | ||||||
| chr1:175135660
|
G | T | 305 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(302): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.3331-185G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135660 | ||||||
| chr1:175135678
|
T | C | 4 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(1): Show | 4 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3331-167T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 15/18 | chr1 | 175135678 | ||||||
| chr1:175136293
|
G | A | 1 | a0002c0079t0001g0095 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3427+352G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136293 | ||||||
| chr1:175136417
|
G | A | 60 | a0003c0015t0001g0312a0003c0015t0003g0261a0003c0015t0003g0263others(57): Show | 60 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.3428-404G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136417 | ||||||
| chr1:175136439
|
A | G | 9 | a0002c0009t0001g0036a0002c0009t0001g0037a0002c0009t0001g0039others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3428-382A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136439 | ||||||
| chr1:175136451
|
A | G | 301 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(298): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.3428-370A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136451 | ||||||
| chr1:175136642
|
T | C | 71 | a0001c0001t0001g0164a0001c0042t0001g0097a0002c0005t0001g0129others(68): Show | 71 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(68): Show |
intron_variant | MODIFIER | c.3428-179T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136642 | ||||||
| chr1:175136744
|
G | A | 230 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.3428-77G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136744 | ||||||
| chr1:175136806
|
G | A | 369 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(366): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.3428-15G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 16/18 | chr1 | 175136806 | ||||||
| chr1:175137050
|
T | C | 5 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(2): Show | 5 | HG01192.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3595+62T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137050 | ||||||
| chr1:175137053
|
C | T | 2 | a0036c0090t0005g0102a0051c0066t0010g0167 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3595+65C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137053 | ||||||
| chr1:175137228
|
A | G | 9 | a0002c0009t0001g0036a0002c0009t0001g0037a0002c0009t0001g0039others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3595+240A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137228 | ||||||
| chr1:175137363
|
A | AGT | 10 | a0001c0016t0001g0040a0002c0005t0002g0019a0003c0002t0001g0295others(7): Show | 10 | HG02486.hp2 HG02559.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.3595+403_3595+404d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175137363 | |||||
| chr1:175137363
|
A | ATGTGTGT others(6): Show |
1 | a0002c0005t0003g0149 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3595+375_3595+376i others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137363 | ||||||
| chr1:175137363
|
AGT | A | 51 | a0004c0019t0001g0223a0005c0003t0001g0169a0005c0003t0001g0176others(48): Show | 51 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.3595+403_3595+404d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175137363 | |||||
| chr1:175137363
|
AGTGTGTG others(3): Show |
A | 9 | a0002c0009t0001g0036a0002c0009t0001g0037a0002c0009t0001g0039others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3595+395_3595+404d others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175137363 | |||||
| chr1:175137393
|
A | T | 235 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.3595+405A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137393 | ||||||
| chr1:175137394
|
T | G | 235 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.3595+406T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137394 | ||||||
| chr1:175137396
|
A | G | 236 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.3595+408A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137396 | ||||||
| chr1:175137397
|
T | A | 12 | a0001c0001t0001g0018a0001c0001t0001g0074a0001c0016t0001g0359others(9): Show | 12 | HG00639.hp2 HG01884.hp1 HG03139.hp2 others(9): Show |
intron_variant | MODIFIER | c.3595+409T>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | ||||||
| chr1:175137397
|
T | TGA | 14 | a0001c0001t0001g0332a0001c0016t0001g0356a0002c0009t0003g0365others(11): Show | 14 | HG01517.hp2 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.3595+409_3595+410i others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | ||||||
| chr1:175137397
|
T | TGTGA | 85 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0070others(82): Show | 86 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.3595+409_3595+410i others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | ||||||
| chr1:175137397
|
T | TGTGTGA | 50 | a0001c0001t0001g0031a0001c0001t0001g0352a0001c0028t0001g0364others(47): Show | 50 | HG00408.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.3595+409_3595+410i others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | ||||||
| chr1:175137397
|
T | TGTGTGTG others(1): Show |
17 | a0003c0002t0001g0278a0003c0002t0001g0292a0003c0002t0001g0297others(14): Show | 17 | HG00280.hp1 HG01069.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.3595+409_3595+410i others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | ||||||
| chr1:175137397
|
T | TGTGTGTG others(3): Show |
44 | a0002c0005t0001g0121a0002c0005t0003g0150a0003c0002t0001g0266others(41): Show | 44 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.3595+409_3595+410i others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | ||||||
| chr1:175137397
|
T | TGTGTGTG others(5): Show |
14 | a0001c0001t0001g0331a0002c0009t0001g0049a0003c0015t0001g0264others(11): Show | 14 | HG00099.hp2 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.3595+409_3595+410i others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137397 | ||||||
| chr1:175137480
|
T | C | 97 | a0002c0005t0001g0121a0003c0002t0001g0266a0003c0002t0001g0270others(94): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3595+492T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137480 | ||||||
| chr1:175137535
|
C | A | 5 | a0001c0031t0005g0075a0001c0031t0005g0156a0001c0031t0005g0330others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3595+547C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137535 | ||||||
| chr1:175137711
|
C | T | 1 | a0029c0096t0001g0308 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3595+723C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137711 | ||||||
| chr1:175137723
|
T | C | 236 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.3595+735T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137723 | ||||||
| chr1:175137739
|
AGTGTTTT others(11): Show |
A | 3 | a0017c0025t0001g0093a0017c0025t0001g0098a0049c0053t0001g0231 | 3 | NA18955.hp1 NA19060.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.3595+768_3595+785d others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175137739 | |||||
| chr1:175137804
|
T | C | 3 | a0001c0016t0001g0356a0013c0014t0001g0056a0013c0014t0001g0069 | 3 | HG01358.hp1 HG01517.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3595+816T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137804 | ||||||
| chr1:175137865
|
A | C | 2 | a0036c0090t0005g0102a0051c0066t0010g0167 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3595+877A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137865 | ||||||
| chr1:175137990
|
C | A | 1 | a0008c0007t0002g0137 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3595+1002C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175137990 | ||||||
| chr1:175138050
|
G | A | 1 | a0006c0004t0001g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3595+1062G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138050 | ||||||
| chr1:175138060
|
G | T | 4 | a0002c0005t0002g0019a0002c0005t0002g0022a0004c0008t0002g0208others(1): Show | 4 | NA18944.hp1 NA18957.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.3595+1072G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138060 | ||||||
| chr1:175138068
|
G | T | 5 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(2): Show | 5 | HG01192.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3595+1080G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138068 | ||||||
| chr1:175138128
|
T | C | 236 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.3595+1140T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138128 | ||||||
| chr1:175138250
|
A | C | 5 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(2): Show | 5 | HG01192.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3595+1262A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138250 | ||||||
| chr1:175138365
|
A | G | 102 | a0001c0001t0001g0331a0002c0005t0001g0121a0002c0009t0001g0049others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3595+1377A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138365 | ||||||
| chr1:175138458
|
T | C | 5 | a0007c0006t0001g0337a0007c0006t0001g0369a0007c0006t0001g0371others(2): Show | 5 | HG02280.hp1 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.3595+1470T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138458 | ||||||
| chr1:175138621
|
A | G | 2 | a0007c0006t0001g0061a0022c0059t0001g0175 | 2 | HG01069.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3595+1633A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138621 | ||||||
| chr1:175138690
|
C | T | 87 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(84): Show | 88 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.3595+1702C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138690 | ||||||
| chr1:175138735
|
G | T | 2 | a0010c0010t0001g0110a0010c0010t0001g0112 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3595+1747G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175138735 | ||||||
| chr1:175139274
|
G | A | 51 | a0004c0019t0001g0223a0005c0003t0001g0169a0005c0003t0001g0176others(48): Show | 51 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.3595+2286G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139274 | ||||||
| chr1:175139493
|
G | T | 236 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.3595+2505G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139493 | ||||||
| chr1:175139614
|
G | A | 2 | a0036c0090t0005g0102a0051c0066t0010g0167 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3595+2626G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139614 | ||||||
| chr1:175139615
|
A | AT | 233 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.3595+2636dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175139615 | |||||
| chr1:175139696
|
A | G | 236 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.3595+2708A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139696 | ||||||
| chr1:175139883
|
C | T | 1 | a0002c0005t0002g0347 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3595+2895C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139883 | ||||||
| chr1:175139911
|
T | C | 6 | a0002c0029t0001g0055a0007c0006t0001g0006a0007c0006t0001g0007others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3595+2923T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139911 | ||||||
| chr1:175139917
|
T | C | 1 | a0053c0065t0001g0268 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3595+2929T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175139917 | ||||||
| chr1:175140066
|
G | A | 1 | a0004c0019t0001g0353 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3595+3078G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140066 | ||||||
| chr1:175140266
|
A | G | 9 | a0002c0009t0001g0036a0002c0009t0001g0037a0002c0009t0001g0039others(6): Show | 9 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3595+3278A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140266 | ||||||
| chr1:175140356
|
T | G | 102 | a0001c0001t0001g0331a0002c0005t0001g0121a0002c0009t0001g0049others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3595+3368T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140356 | ||||||
| chr1:175140364
|
G | T | 51 | a0004c0019t0001g0223a0005c0003t0001g0169a0005c0003t0001g0176others(48): Show | 51 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.3595+3376G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140364 | ||||||
| chr1:175140381
|
G | A | 102 | a0001c0001t0001g0331a0002c0005t0001g0121a0002c0009t0001g0049others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3595+3393G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140381 | ||||||
| chr1:175140491
|
C | G | 78 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(75): Show | 79 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.3595+3503C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140491 | ||||||
| chr1:175140586
|
A | G | 246 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.3595+3598A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140586 | ||||||
| chr1:175140703
|
T | G | 1 | a0011c0011t0003g0189 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3596-3684T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140703 | ||||||
| chr1:175140748
|
C | T | 50 | a0004c0019t0001g0223a0005c0003t0001g0169a0005c0003t0001g0176others(47): Show | 50 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.3596-3639C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140748 | ||||||
| chr1:175140780
|
C | T | 9 | a0001c0001t0001g0070a0001c0001t0001g0128a0001c0001t0001g0332others(6): Show | 9 | HG02486.hp1 HG02572.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.3596-3607C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140780 | ||||||
| chr1:175140795
|
A | G | 1 | a0033c0072t0004g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3596-3592A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140795 | ||||||
| chr1:175140837
|
T | C | 2 | a0024c0039t0009g0010a0024c0039t0009g0012 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3596-3550T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175140837 | ||||||
| chr1:175141027
|
G | A | 35 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(32): Show | 36 | HG00099.hp1 HG00544.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.3596-3360G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141027 | ||||||
| chr1:175141055
|
G | T | 2 | a0036c0090t0005g0102a0051c0066t0010g0167 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3596-3332G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141055 | ||||||
| chr1:175141121
|
A | C | 2 | a0024c0039t0009g0010a0024c0039t0009g0012 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3596-3266A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141121 | ||||||
| chr1:175141210
|
G | A | 1 | a0033c0072t0004g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3596-3177G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141210 | ||||||
| chr1:175141344
|
C | T | 101 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.3596-3043C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141344 | ||||||
| chr1:175141381
|
C | T | 2 | a0036c0090t0005g0102a0051c0066t0010g0167 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3596-3006C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141381 | ||||||
| chr1:175141763
|
C | A | 1 | a0001c0001t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3596-2624C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141763 | ||||||
| chr1:175141816
|
C | T | 2 | a0024c0039t0009g0010a0024c0039t0009g0012 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3596-2571C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141816 | ||||||
| chr1:175141819
|
C | A | 96 | a0001c0001t0002g0122a0001c0001t0002g0163a0001c0016t0001g0040others(93): Show | 98 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.3596-2568C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141819 | ||||||
| chr1:175141898
|
A | G | 1 | a0006c0004t0001g0253 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3596-2489A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141898 | ||||||
| chr1:175141964
|
C | A | 1 | a0004c0019t0001g0209 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3596-2423C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175141964 | ||||||
| chr1:175142217
|
C | T | 3 | a0001c0001t0001g0020a0002c0005t0003g0150a0009c0012t0003g0273 | 3 | HG01109.hp2 HG02071.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3596-2170C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142217 | ||||||
| chr1:175142233
|
G | A | 33 | a0002c0005t0003g0103a0002c0005t0003g0105a0002c0005t0003g0106others(30): Show | 33 | HG01109.hp2 HG01192.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.3596-2154G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142233 | ||||||
| chr1:175142269
|
C | T | 1 | a0002c0009t0003g0362 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3596-2118C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142269 | ||||||
| chr1:175142398
|
C | CTTATTTT others(52): Show |
1 | a0004c0008t0002g0225 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3596-1950_3596-194 others(63): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175142398 | |||||
| chr1:175142438
|
C | T | 368 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(365): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.3596-1949C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142438 | ||||||
| chr1:175142470
|
C | CAAAT | 264 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.3596-1915_3596-191 others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175142470 | |||||
| chr1:175142499
|
C | T | 5 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(2): Show | 5 | HG01192.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3596-1888C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142499 | ||||||
| chr1:175142512
|
G | A | 1 | a0024c0039t0009g0012 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3596-1875G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142512 | ||||||
| chr1:175142624
|
C | CT | 89 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(86): Show | 90 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.3596-1752dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175142624 | |||||
| chr1:175142711
|
G | A | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3596-1676G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142711 | ||||||
| chr1:175142782
|
C | T | 365 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(362): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.3596-1605C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142782 | ||||||
| chr1:175142806
|
C | T | 3 | a0009c0021t0001g0004a0021c0027t0001g0219a0021c0027t0001g0222 | 3 | HG00639.hp1 HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3596-1581C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142806 | ||||||
| chr1:175142810
|
G | A | 100 | a0001c0001t0001g0331a0002c0005t0001g0119a0002c0009t0001g0049others(97): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.3596-1577G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142810 | ||||||
| chr1:175142817
|
C | T | 264 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.3596-1570C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142817 | ||||||
| chr1:175142905
|
C | G | 4 | a0005c0003t0001g0255a0016c0020t0001g0078a0016c0020t0001g0080others(1): Show | 4 | NA18956.hp2 NA18989.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.3596-1482C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142905 | ||||||
| chr1:175142962
|
C | T | 1 | a0001c0001t0001g0323 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3596-1425C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175142962 | ||||||
| chr1:175143026
|
C | T | 2 | a0004c0019t0001g0353a0006c0004t0001g0243 | 2 | HG01346.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.3596-1361C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175143026 | ||||||
| chr1:175143182
|
C | T | 3 | a0001c0016t0001g0040a0037c0080t0001g0165a0044c0087t0001g0335 | 3 | HG02145.hp2 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3596-1205C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175143182 | ||||||
| chr1:175143228
|
TGAGATGA others(52): Show |
T | 1 | a0004c0008t0002g0225 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3596-1156_3596-109 others(63): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143228 | |||||
| chr1:175143518
|
G | GGTGT | 10 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(7): Show | 10 | HG01192.hp2 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.3596-852_3596-849d others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143518 | |||||
| chr1:175143518
|
G | GGTGTGT | 46 | a0001c0016t0001g0040a0002c0005t0003g0103a0002c0005t0003g0105others(43): Show | 47 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.3596-854_3596-849d others(8): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143518 | |||||
| chr1:175143518
|
G | GGTGTGTG others(1): Show |
140 | a0001c0001t0001g0331a0001c0042t0001g0097a0002c0005t0001g0119others(137): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.3596-856_3596-849d others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143518 | |||||
| chr1:175143518
|
G | GGTGTGTG others(3): Show |
20 | a0002c0009t0001g0036a0003c0002t0001g0266a0005c0003t0001g0180others(17): Show | 20 | HG01433.hp1 HG01978.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.3596-858_3596-849d others(12): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143518 | |||||
| chr1:175143518
|
G | GGTGTGTG others(5): Show |
93 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0031others(90): Show | 94 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.3596-860_3596-849d others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143518 | |||||
| chr1:175143518
|
G | GGTGTGTG others(7): Show |
4 | a0001c0089t0001g0024a0007c0006t0015g0011a0013c0014t0001g0069others(1): Show | 4 | HG03130.hp2 HG03927.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.3596-862_3596-849d others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143518 | |||||
| chr1:175143531
|
G | GTGTT | 51 | a0001c0001t0002g0122a0001c0001t0002g0163a0002c0005t0002g0019others(48): Show | 52 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.3596-853_3596-852i others(6): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143531 | |||||
| chr1:175143608
|
G | C | 1 | a0003c0002t0001g0283 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3596-779G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175143608 | ||||||
| chr1:175143622
|
T | G | 3 | a0002c0005t0002g0342a0004c0008t0002g0206a0009c0012t0002g0326 | 3 | HG02135.hp2 HG02523.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.3596-765T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175143622 | ||||||
| chr1:175143931
|
GTA | G | 160 | a0001c0001t0001g0331a0001c0042t0001g0097a0002c0005t0001g0119others(157): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.3596-454_3596-453d others(4): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175143931 | |||||
| chr1:175143982
|
T | G | 264 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.3596-405T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175143982 | ||||||
| chr1:175144048
|
T | G | 365 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(362): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.3596-339T>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175144048 | ||||||
| chr1:175144114
|
A | C | 5 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(2): Show | 5 | HG01192.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3596-273A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175144114 | ||||||
| chr1:175144228
|
TC | T | 3 | a0002c0009t0001g0041a0002c0009t0001g0043a0002c0009t0013g0048 | 3 | HG02257.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3596-156delC | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 175144228 | |||||
| chr1:175144369
|
G | A | 1 | a0005c0003t0001g0199 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3596-18G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 17/18 | chr1 | 175144369 | ||||||
| chr1:175144879
|
T | C | 35 | a0002c0005t0003g0103a0002c0005t0003g0105a0002c0005t0003g0106others(32): Show | 35 | HG01109.hp2 HG01192.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.3759+329T>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175144879 | ||||||
| chr1:175145062
|
A | T | 2 | a0007c0006t0001g0061a0022c0059t0001g0175 | 2 | HG01069.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3759+512A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145062 | ||||||
| chr1:175145156
|
G | T | 1 | a0019c0023t0001g0309 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3759+606G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145156 | ||||||
| chr1:175145337
|
G | A | 264 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.3759+787G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145337 | ||||||
| chr1:175145539
|
C | A | 263 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(260): Show | 264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.3759+989C>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145539 | ||||||
| chr1:175145552
|
C | CA | 8 | a0002c0005t0003g0149a0003c0015t0003g0267a0004c0008t0003g0246others(5): Show | 8 | HG00609.hp2 HG01109.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.3759+1025dupA | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | |||||
| chr1:175145552
|
C | CAAAAAA | 74 | a0001c0001t0001g0331a0002c0005t0001g0119a0002c0009t0001g0049others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.3759+1020_3759+102 others(10): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | |||||
| chr1:175145552
|
C | CAAAAAAA | 25 | a0001c0028t0001g0364a0001c0028t0007g0044a0001c0028t0007g0046others(22): Show | 25 | HG00438.hp2 HG00738.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.3759+1019_3759+102 others(11): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | |||||
| chr1:175145552
|
C | CAAAAAAA others(2): Show |
44 | a0002c0005t0001g0121a0002c0009t0001g0036a0003c0002t0001g0287others(41): Show | 44 | HG00323.hp2 HG01243.hp1 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.3759+1017_3759+102 others(13): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | |||||
| chr1:175145552
|
C | CAAAAAAA others(3): Show |
13 | a0001c0042t0001g0097a0005c0003t0001g0176a0005c0003t0001g0186others(10): Show | 13 | HG01243.hp2 HG01928.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.3759+1016_3759+102 others(14): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | |||||
| chr1:175145552
|
C | CAAAAAAA others(4): Show |
6 | a0014c0024t0001g0370a0016c0020t0001g0147a0017c0025t0001g0093others(3): Show | 6 | HG00642.hp2 HG03139.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3759+1015_3759+102 others(15): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | |||||
| chr1:175145552
|
C | CAAAAAAA others(5): Show |
4 | a0003c0002t0012g0277a0011c0011t0001g0197a0011c0011t0001g0238others(1): Show | 4 | HG00408.hp1 HG02698.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3759+1014_3759+102 others(16): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | |||||
| chr1:175145552
|
C | CAAAAAAA others(6): Show |
6 | a0001c0001t0001g0333a0001c0016t0001g0358a0002c0009t0001g0037others(3): Show | 6 | HG01261.hp2 HG01358.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3759+1013_3759+102 others(17): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | |||||
| chr1:175145552
|
C | CAAAAAAA others(7): Show |
34 | a0001c0001t0001g0018a0001c0001t0001g0074a0001c0001t0001g0107others(31): Show | 35 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.3759+1012_3759+102 others(18): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | |||||
| chr1:175145552
|
C | CAAAAAAA others(8): Show |
44 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0031others(41): Show | 44 | HG00544.hp1 HG00738.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.3759+1011_3759+102 others(19): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | |||||
| chr1:175145552
|
C | CAAAAAAA others(9): Show |
11 | a0001c0001t0001g0070a0001c0001t0001g0123a0001c0001t0001g0128others(8): Show | 11 | HG01081.hp2 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3759+1010_3759+102 others(20): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175145552 | |||||
| chr1:175145675
|
A | T | 3 | a0001c0001t0001g0334a0001c0042t0001g0059a0019c0023t0001g0241 | 3 | HG02486.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3759+1125A>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145675 | ||||||
| chr1:175145700
|
G | T | 1 | a0007c0006t0001g0153 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3759+1150G>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145700 | ||||||
| chr1:175145769
|
C | T | 4 | a0003c0002t0001g0300a0007c0006t0001g0117a0007c0006t0001g0118others(1): Show | 4 | NA18945.hp2 NA18999.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.3760-1162C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145769 | ||||||
| chr1:175145770
|
G | A | 61 | a0001c0001t0002g0122a0001c0001t0002g0163a0001c0016t0001g0040others(58): Show | 63 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.3760-1161G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145770 | ||||||
| chr1:175145806
|
C | T | 2 | a0007c0006t0001g0006a0007c0006t0001g0007 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3760-1125C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145806 | ||||||
| chr1:175145912
|
G | C | 365 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(362): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.3760-1019G>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175145912 | ||||||
| chr1:175146124
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0128a0001c0074t0001g0052 | 3 | HG02572.hp2 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3760-807C>T | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175146124 | ||||||
| chr1:175146233
|
CCTGAACC others(12): Show |
C | 1 | a0012c0013t0001g0101 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3760-695_3760-677d others(21): Show |
TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175146233 | |||||
| chr1:175146431
|
A | C | 259 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(256): Show | 260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3760-500A>C | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175146431 | ||||||
| chr1:175146603
|
G | A | 5 | a0001c0031t0005g0075a0001c0031t0005g0156a0001c0031t0005g0330others(2): Show | 5 | HG01884.hp1 HG02622.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.3760-328G>A | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175146603 | ||||||
| chr1:175146646
|
A | G | 1 | a0020c0022t0001g0289 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3760-285A>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175146646 | ||||||
| chr1:175146729
|
C | G | 3 | a0002c0005t0002g0019a0002c0005t0002g0022a0004c0008t0002g0208 | 3 | NA18944.hp1 NA18957.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.3760-202C>G | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | chr1 | 175146729 | ||||||
| chr1:175146910
|
C | CT | 263 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(260): Show | 264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
splice_region_variant&intron_variant | LOW | c.3760-6dupT | TNN | ENSG00000120332.17 | transcript | ENST00000239462.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 175146910 |