| geneid | 3371 |
|---|---|
| ensemblid | ENSG00000041982.17 |
| hgncid | 5318 |
| symbol | TNC |
| name | tenascin C |
| refseq_nuc | NM_002160.4 |
| refseq_prot | NP_002151.2 |
| ensembl_nuc | ENST00000350763.9 |
| ensembl_prot | ENSP00000265131.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 115019575 |
| end | 115118157 |
| strand | - |
| ver | v1.2 |
| region | chr9:115019575-115118157 |
| region5000 | chr9:115014575-115123157 |
| regionname0 | TNC_chr9_115019575_115118157 |
| regionname5000 | TNC_chr9_115014575_115123157 |
| 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 | 2201 | 50 | 7 | 10 | 21 | 4 | 8 | 20 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002 | 0/0 | 2201 | 47 | 2 | 10 | 26 | 1 | 8 | 21 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003 | 0/0 | 2201 | 39 | 9 | 4 | 23 | 1 | 2 | 21 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004 | 0/0 | 2201 | 31 | 6 | 6 | 12 | 0 | 7 | 9 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005 | 0/0 | 2201 | 24 | 5 | 10 | 2 | 2 | 5 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0006 | 0/0 | 2201 | 18 | 3 | 8 | 7 | 0 | 0 | 5 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0007 | 0/0 | 2201 | 17 | 0 | 0 | 15 | 0 | 2 | 11 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0008 | 0/0 | 2201 | 15 | 0 | 5 | 1 | 5 | 4 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009 | 0/0 | 2201 | 15 | 2 | 5 | 5 | 0 | 3 | 2 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0010 | 0/0 | 2201 | 12 | 0 | 0 | 11 | 0 | 1 | 8 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0011 | 0/0 | 2201 | 11 | 6 | 0 | 4 | 0 | 1 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0012 | 0/0 | 2201 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0013 | 0/0 | 2201 | 5 | 4 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0014 | 0/0 | 2201 | 5 | 2 | 3 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0015 | 0/0 | 2201 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0016 | 0/0 | 2201 | 4 | 1 | 0 | 3 | 0 | 0 | 3 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0017 | 0/0 | 2201 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0018 | 0/0 | 2201 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0019 | 0/1 | 2201 | 3 | 0 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0020 | 0/0 | 2201 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0021 | 0/0 | 2201 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0022 | 0/0 | 2201 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0023 | 0/0 | 2201 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0024 | 0/0 | 2201 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0025 | 0/0 | 2201 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0026 | 0/0 | 2201 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0027 | 0/0 | 2201 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0028 | 0/0 | 2201 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0029 | 0/0 | 2201 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0030 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0031 | 0/0 | 2201 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0032 | 1/0 | 2201 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0033 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0034 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0035 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0036 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0037 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0038 | 0/0 | 2201 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0039 | 0/0 | 2201 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0040 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0041 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0042 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0043 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0044 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0045 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0046 | 0/0 | 2201 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0047 | 0/0 | 2201 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0048 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0049 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0050 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0051 | 0/0 | 2201 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0052 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0053 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0054 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0055 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0056 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| 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 | 6606 | 39 | 1 | 10 | 21 | 1 | 6 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0002 | 0/0 | 6606 | 26 | 3 | 7 | 9 | 4 | 3 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0003 | 0/0 | 6606 | 23 | 2 | 3 | 16 | 1 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0004 | 0/0 | 6606 | 19 | 0 | 3 | 11 | 0 | 5 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0005 | 0/0 | 6606 | 15 | 0 | 5 | 1 | 5 | 4 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0006 | 0/0 | 6606 | 14 | 0 | 0 | 14 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0007 | 0/0 | 6606 | 13 | 3 | 6 | 4 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0008 | 0/0 | 6606 | 12 | 0 | 0 | 11 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0009 | 0/0 | 6606 | 12 | 3 | 2 | 4 | 0 | 3 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0010 | 0/0 | 6606 | 10 | 6 | 0 | 3 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0011 | 0/0 | 6606 | 7 | 0 | 1 | 5 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0012 | 0/0 | 6606 | 7 | 7 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0013 | 0/0 | 6606 | 6 | 0 | 1 | 4 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0014 | 0/0 | 6606 | 6 | 0 | 5 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0015 | 0/0 | 6606 | 5 | 0 | 2 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0016 | 0/0 | 6606 | 5 | 2 | 3 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0017 | 0/0 | 6606 | 5 | 0 | 1 | 1 | 0 | 3 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0018 | 0/0 | 6606 | 5 | 3 | 0 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0019 | 0/0 | 6606 | 5 | 0 | 4 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0020 | 0/0 | 6606 | 5 | 0 | 0 | 5 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0021 | 0/0 | 6606 | 4 | 4 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0022 | 0/0 | 6606 | 4 | 4 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0023 | 0/0 | 6606 | 4 | 0 | 1 | 0 | 2 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0024 | 0/0 | 6606 | 4 | 1 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0025 | 0/0 | 6606 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0026 | 0/1 | 6606 | 3 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0027 | 0/0 | 6606 | 3 | 3 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0028 | 0/0 | 6606 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0029 | 0/0 | 6606 | 3 | 0 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0030 | 0/0 | 6606 | 3 | 0 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0031 | 0/0 | 6606 | 3 | 0 | 1 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0032 | 0/0 | 6606 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0033 | 0/0 | 6606 | 3 | 3 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0034 | 0/0 | 6606 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0035 | 0/0 | 6606 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0036 | 0/0 | 6606 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0037 | 0/0 | 6606 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0038 | 0/0 | 6606 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0039 | 0/0 | 6606 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0040 | 0/0 | 6606 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0041 | 0/0 | 6606 | 2 | 0 | 0 | 0 | 0 | 2 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0042 | 0/0 | 6606 | 2 | 0 | 0 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0043 | 0/0 | 6606 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0044 | 0/0 | 6606 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0045 | 0/0 | 6606 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0046 | 0/0 | 6606 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0047 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0048 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0049 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0050 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0051 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0052 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0053 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0054 | 0/0 | 6606 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0055 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0056 | 0/0 | 6606 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0057 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0058 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0059 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0060 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0061 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0062 | 0/0 | 6606 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0063 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0064 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0065 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0066 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0067 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0068 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0069 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0070 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0071 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0072 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0073 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0074 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0075 | 0/0 | 6606 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0076 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0077 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0078 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0079 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0080 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0081 | 1/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0082 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0083 | 0/0 | 6606 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0084 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0085 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0086 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0087 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0088 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0089 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0090 | 0/0 | 6606 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0091 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0092 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0093 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0094 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0095 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0096 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0097 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0098 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0099 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0100 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0101 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0102 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0103 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| c0104 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| 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 | 0/0 | 1897 | 115 | 20 | 25 | 45 | 9 | 16 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0002 | 1/0 | 1895 | 88 | 14 | 17 | 33 | 2 | 21 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0003 | 0/0 | 1897 | 25 | 1 | 0 | 24 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0004 | 0/0 | 1895 | 25 | 22 | 1 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0005 | 0/0 | 1896 | 22 | 7 | 8 | 7 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0006 | 0/1 | 1896 | 17 | 10 | 6 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0007 | 0/0 | 1895 | 13 | 0 | 0 | 12 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0008 | 0/0 | 1897 | 11 | 0 | 1 | 6 | 0 | 4 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0009 | 0/0 | 1896 | 6 | 0 | 0 | 6 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0010 | 0/0 | 1896 | 6 | 0 | 2 | 2 | 2 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0011 | 0/0 | 1894 | 5 | 0 | 4 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0012 | 0/0 | 1897 | 5 | 4 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0013 | 0/0 | 1898 | 4 | 1 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0014 | 0/0 | 1897 | 4 | 4 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0015 | 0/0 | 1898 | 3 | 3 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0016 | 0/0 | 1896 | 2 | 0 | 0 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0017 | 0/0 | 1894 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0018 | 0/0 | 1897 | 2 | 0 | 1 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0019 | 0/0 | 1896 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0020 | 0/0 | 1895 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0021 | 0/0 | 1896 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0022 | 0/0 | 1896 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0023 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0024 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0025 | 0/0 | 1895 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0026 | 0/0 | 1897 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0027 | 0/0 | 1895 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| t0028 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| 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 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 6606 | 26 | 3 | 7 | 9 | 4 | 3 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0009 | 0/0 | 6606 | 12 | 3 | 2 | 4 | 0 | 3 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0011 | 0/0 | 6606 | 7 | 0 | 1 | 5 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0024 | 0/0 | 6606 | 4 | 1 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0094 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0001 | 0/0 | 6606 | 39 | 1 | 10 | 21 | 1 | 6 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0020 | 0/0 | 6606 | 5 | 0 | 0 | 5 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0093 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0096 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0098 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0003 | 0/0 | 6606 | 23 | 2 | 3 | 16 | 1 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0013 | 0/0 | 6606 | 6 | 0 | 1 | 4 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0027 | 0/0 | 6606 | 3 | 3 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0035 | 0/0 | 6606 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0052 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0055 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0068 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0069 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0077 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0004 | 0/0 | 6606 | 19 | 0 | 3 | 11 | 0 | 5 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0018 | 0/0 | 6606 | 5 | 3 | 0 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0045 | 0/0 | 6606 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0050 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0051 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0073 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0074 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0075 | 0/0 | 6606 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0014 | 0/0 | 6606 | 6 | 0 | 5 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0017 | 0/0 | 6606 | 5 | 0 | 1 | 1 | 0 | 3 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0023 | 0/0 | 6606 | 4 | 0 | 1 | 0 | 2 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0034 | 0/0 | 6606 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0037 | 0/0 | 6606 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0061 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0062 | 0/0 | 6606 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0066 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0067 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0103 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0006c0007 | 0/0 | 6606 | 13 | 3 | 6 | 4 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0006c0015 | 0/0 | 6606 | 5 | 0 | 2 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0007c0006 | 0/0 | 6606 | 14 | 0 | 0 | 14 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0007c0041 | 0/0 | 6606 | 2 | 0 | 0 | 0 | 0 | 2 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0007c0086 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0008c0005 | 0/0 | 6606 | 15 | 0 | 5 | 1 | 5 | 4 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0019 | 0/0 | 6606 | 5 | 0 | 4 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0031 | 0/0 | 6606 | 3 | 0 | 1 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0042 | 0/0 | 6606 | 2 | 0 | 0 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0044 | 0/0 | 6606 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0092 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0099 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0100 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0010c0008 | 0/0 | 6606 | 12 | 0 | 0 | 11 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0011c0010 | 0/0 | 6606 | 10 | 6 | 0 | 3 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0011c0076 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0012c0012 | 0/0 | 6606 | 7 | 7 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0013c0021 | 0/0 | 6606 | 4 | 4 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0013c0059 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0014c0016 | 0/0 | 6606 | 5 | 2 | 3 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0015c0029 | 0/0 | 6606 | 3 | 0 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0015c0040 | 0/0 | 6606 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0016c0043 | 0/0 | 6606 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0016c0095 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0016c0101 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0017c0022 | 0/0 | 6606 | 4 | 4 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0018c0028 | 0/0 | 6606 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0019c0026 | 0/1 | 6606 | 3 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0020c0030 | 0/0 | 6606 | 3 | 0 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0021c0032 | 0/0 | 6606 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0022c0025 | 0/0 | 6606 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0023c0033 | 0/0 | 6606 | 3 | 3 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0024c0082 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0024c0083 | 0/0 | 6606 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0025c0039 | 0/0 | 6606 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0026c0036 | 0/0 | 6606 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0027c0070 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0027c0071 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0028c0038 | 0/0 | 6606 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0029c0046 | 0/0 | 6606 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0030c0047 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0031c0056 | 0/0 | 6606 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0032c0081 | 1/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0033c0058 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0034c0060 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0035c0085 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0036c0087 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0037c0084 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0038c0088 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0039c0090 | 0/0 | 6606 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0040c0091 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0041c0102 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0042c0089 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0043c0048 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0044c0065 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0045c0049 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0046c0053 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0047c0054 | 0/0 | 6606 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0048c0072 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0049c0064 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0050c0063 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0051c0097 | 0/0 | 6606 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0052c0057 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0053c0104 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0054c0080 | 0/0 | 6606 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0055c0079 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0056c0078 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 8502 | 18 | 3 | 6 | 4 | 3 | 2 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0002t0003 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0002t0008 | 0/0 | 8502 | 4 | 0 | 0 | 3 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0002t0010 | 0/0 | 8501 | 2 | 0 | 1 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0002t0013 | 0/0 | 8503 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0009t0001 | 0/0 | 8502 | 7 | 0 | 2 | 2 | 0 | 3 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0009t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0009t0010 | 0/0 | 8501 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0009t0015 | 0/0 | 8503 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0011t0001 | 0/0 | 8502 | 5 | 0 | 0 | 4 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0011t0008 | 0/0 | 8502 | 2 | 0 | 1 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0024t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0024t0003 | 0/0 | 8502 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0024t0015 | 0/0 | 8503 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0001c0094t0008 | 0/0 | 8502 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0001t0001 | 0/0 | 8502 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0001t0002 | 0/0 | 8500 | 35 | 1 | 9 | 18 | 1 | 6 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0001t0006 | 0/0 | 8501 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0001t0007 | 0/0 | 8500 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0020t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0020t0002 | 0/0 | 8500 | 3 | 0 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0020t0011 | 0/0 | 8499 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0093t0004 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0096t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0002c0098t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0003t0001 | 0/0 | 8502 | 17 | 1 | 1 | 14 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0003t0003 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0003t0004 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0003t0010 | 0/0 | 8501 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0003t0013 | 0/0 | 8503 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0003t0019 | 0/0 | 8501 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0013t0001 | 0/0 | 8502 | 4 | 0 | 1 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0013t0008 | 0/0 | 8502 | 2 | 0 | 0 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0027t0002 | 0/0 | 8500 | 3 | 3 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0035t0004 | 0/0 | 8500 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0052t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0055t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0068t0013 | 0/0 | 8503 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0069t0005 | 0/0 | 8501 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0003c0077t0004 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0004t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0004t0002 | 0/0 | 8500 | 18 | 0 | 3 | 10 | 0 | 5 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0018t0004 | 0/0 | 8500 | 5 | 3 | 0 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0045t0002 | 0/0 | 8500 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0050t0014 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0051t0004 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0073t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0074t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0004c0075t0004 | 0/0 | 8500 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0014t0001 | 0/0 | 8502 | 6 | 0 | 5 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0017t0001 | 0/0 | 8502 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0017t0002 | 0/0 | 8500 | 4 | 0 | 1 | 1 | 0 | 2 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0023t0001 | 0/0 | 8502 | 3 | 0 | 0 | 0 | 2 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0023t0018 | 0/0 | 8502 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0034t0002 | 0/0 | 8500 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0037t0004 | 0/0 | 8500 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0061t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0062t0026 | 0/0 | 8502 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0066t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0067t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0005c0103t0012 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0006c0007t0005 | 0/0 | 8501 | 10 | 2 | 5 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0006c0007t0022 | 0/0 | 8501 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0006c0007t0024 | 0/0 | 8501 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0006c0007t0027 | 0/0 | 8500 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0006c0015t0002 | 0/0 | 8500 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0006c0015t0005 | 0/0 | 8501 | 4 | 0 | 2 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0007c0006t0003 | 0/0 | 8502 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0007c0006t0007 | 0/0 | 8500 | 9 | 0 | 0 | 9 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0007c0006t0016 | 0/0 | 8501 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0007c0006t0017 | 0/0 | 8499 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0007c0041t0007 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0007c0041t0016 | 0/0 | 8501 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0007c0086t0020 | 0/0 | 8500 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0008c0005t0001 | 0/0 | 8502 | 13 | 0 | 4 | 1 | 4 | 4 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0008c0005t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0008c0005t0010 | 0/0 | 8501 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0019t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0019t0011 | 0/0 | 8499 | 4 | 0 | 4 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0031t0001 | 0/0 | 8502 | 3 | 0 | 1 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0042t0008 | 0/0 | 8502 | 2 | 0 | 0 | 1 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0044t0001 | 0/0 | 8502 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0092t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0099t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0009c0100t0005 | 0/0 | 8501 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0010c0008t0001 | 0/0 | 8502 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0010c0008t0003 | 0/0 | 8502 | 9 | 0 | 0 | 9 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0010c0008t0007 | 0/0 | 8500 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0010c0008t0021 | 0/0 | 8501 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0011c0010t0001 | 0/0 | 8502 | 9 | 5 | 0 | 3 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0011c0010t0013 | 0/0 | 8503 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0011c0076t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0012c0012t0006 | 0/0 | 8501 | 7 | 7 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0013c0021t0004 | 0/0 | 8500 | 4 | 4 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0013c0059t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0014c0016t0006 | 0/0 | 8501 | 5 | 2 | 3 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0015c0029t0003 | 0/0 | 8502 | 3 | 0 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0015c0040t0003 | 0/0 | 8502 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0016c0043t0009 | 0/0 | 8501 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0016c0095t0025 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0016c0101t0005 | 0/0 | 8501 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0017c0022t0004 | 0/0 | 8500 | 4 | 4 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0018c0028t0012 | 0/0 | 8502 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0019c0026t0006 | 0/1 | 8501 | 3 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0020c0030t0009 | 0/0 | 8501 | 3 | 0 | 0 | 3 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0021c0032t0001 | 0/0 | 8502 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0022c0025t0001 | 0/0 | 8502 | 3 | 2 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0023c0033t0001 | 0/0 | 8502 | 3 | 3 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0024c0082t0004 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0024c0083t0001 | 0/0 | 8502 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0025c0039t0003 | 0/0 | 8502 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0026c0036t0002 | 0/0 | 8500 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0027c0070t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0027c0071t0001 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0028c0038t0005 | 0/0 | 8501 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0029c0046t0004 | 0/0 | 8500 | 2 | 2 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0030c0047t0001 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0031c0056t0001 | 0/0 | 8502 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0032c0081t0002 | 1/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0033c0058t0001 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0034c0060t0014 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0035c0085t0003 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0036c0087t0003 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0037c0084t0007 | 0/0 | 8500 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0038c0088t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0039c0090t0001 | 0/0 | 8502 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0040c0091t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0041c0102t0001 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0042c0089t0009 | 0/0 | 8501 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0043c0048t0005 | 0/0 | 8501 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0044c0065t0005 | 0/0 | 8501 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0045c0049t0002 | 0/0 | 8500 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0046c0053t0018 | 0/0 | 8502 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0047c0054t0005 | 0/0 | 8501 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0048c0072t0006 | 0/0 | 8501 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0049c0064t0014 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0050c0063t0012 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0051c0097t0002 | 0/0 | 8500 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0052c0057t0014 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0053c0104t0028 | 0/0 | 8501 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0054c0080t0003 | 0/0 | 8502 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0055c0079t0023 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| a0056c0078t0001 | 0/0 | 8502 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | copy fasta | chr9 | 115014575 | 115123157 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0008g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0008g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0008g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0010g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0010g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0002t0013g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0009t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0009t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0009t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0009t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0009t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0009t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0009t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0009t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0009t0010g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0009t0010g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0009t0015g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0009t0015g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0011t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0011t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0011t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0011t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0011t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0011t0008g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0011t0008g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0024t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0024t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0024t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0024t0015g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0001c0094t0008g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0006g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0020t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0020t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0020t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0020t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0020t0011g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0093t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0096t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0002c0098t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0010g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0013g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0019g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0003t0019g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0013t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0013t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0013t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0013t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0013t0008g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0013t0008g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0027t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0027t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0027t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0035t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0035t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0052t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0055t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0068t0013g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0069t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0003c0077t0004g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0004t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0018t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0018t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0018t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0018t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0018t0004g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0045t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0045t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0050t0014g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0051t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0073t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0074t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0004c0075t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0014t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0014t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0014t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0014t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0014t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0017t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0017t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0017t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0017t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0017t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0023t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0023t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0023t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0023t0018g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0034t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0034t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0037t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0037t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0061t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0062t0026g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0066t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0067t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0005c0103t0012g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0007t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0007t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0007t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0007t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0007t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0007t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0007t0005g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0007t0005g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0007t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0007t0005g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0007t0022g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0007t0024g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0007t0027g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0015t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0015t0005g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0015t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0006c0015t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0006t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0006t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0006t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0006t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0006t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0006t0007g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0006t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0006t0007g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0006t0007g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0006t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0006t0016g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0006t0017g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0006t0017g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0041t0007g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0041t0016g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0007c0086t0020g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0008c0005t0010g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0019t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0019t0011g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0019t0011g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0019t0011g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0031t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0031t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0031t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0042t0008g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0042t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0044t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0044t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0092t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0099t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0009c0100t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0010c0008t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0010c0008t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0010c0008t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0010c0008t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0010c0008t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0010c0008t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0010c0008t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0010c0008t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0010c0008t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0010c0008t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0010c0008t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0010c0008t0021g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0011c0010t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0011c0010t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0011c0010t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0011c0010t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0011c0010t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0011c0010t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0011c0010t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0011c0010t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0011c0010t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0011c0010t0013g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0011c0076t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0012c0012t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0012c0012t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0012c0012t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0012c0012t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0012c0012t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0012c0012t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0012c0012t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0013c0021t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0013c0021t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0013c0021t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0013c0021t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0013c0059t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0014c0016t0006g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0014c0016t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0014c0016t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0014c0016t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0014c0016t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0015c0029t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0015c0029t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0015c0029t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0015c0040t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0015c0040t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0016c0043t0009g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0016c0043t0009g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0016c0095t0025g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0016c0101t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0017c0022t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0017c0022t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0017c0022t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0017c0022t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0018c0028t0012g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0018c0028t0012g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0018c0028t0012g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0019c0026t0006g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0019c0026t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0019c0026t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0020c0030t0009g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0020c0030t0009g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0020c0030t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0021c0032t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0021c0032t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0021c0032t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0022c0025t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0022c0025t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0022c0025t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0023c0033t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0023c0033t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0023c0033t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0024c0082t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0024c0083t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0025c0039t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0025c0039t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0026c0036t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0026c0036t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0027c0070t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0027c0071t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0028c0038t0005g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0028c0038t0005g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0029c0046t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0029c0046t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0030c0047t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0031c0056t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0032c0081t0002g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0033c0058t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0034c0060t0014g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0035c0085t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0036c0087t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0037c0084t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0038c0088t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0039c0090t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0040c0091t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0041c0102t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0042c0089t0009g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0043c0048t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0044c0065t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0045c0049t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0046c0053t0018g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0047c0054t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0048c0072t0006g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0049c0064t0014g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0050c0063t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0051c0097t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0052c0057t0014g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0053c0104t0028g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0054c0080t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0055c0079t0023g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| a0056c0078t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0005 | c0023 | t0001 | g0300 | EUR | GBR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00099 | hp2 | a0008 | c0005 | t0001 | g0115 | EUR | GBR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0290 | EUR | GBR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00140 | hp2 | a0008 | c0005 | t0001 | g0084 | EUR | GBR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00280 | hp1 | a0008 | c0005 | t0002 | g0187 | EUR | FIN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00280 | hp2 | a0001 | c0002 | t0010 | g0288 | EUR | FIN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00323 | hp1 | a0046 | c0053 | t0018 | g0245 | EUR | FIN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00323 | hp2 | a0005 | c0023 | t0001 | g0299 | EUR | FIN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00408 | hp1 | a0007 | c0086 | t0020 | g0044 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00408 | hp2 | a0007 | c0006 | t0007 | g0019 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00423 | hp1 | a0004 | c0004 | t0002 | g0310 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00423 | hp2 | a0010 | c0008 | t0003 | g0015 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00558 | hp1 | a0007 | c0006 | t0003 | g0028 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00558 | hp2 | a0007 | c0006 | t0007 | g0045 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00597 | hp1 | a0003 | c0013 | t0001 | g0285 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00597 | hp2 | a0010 | c0008 | t0003 | g0013 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00609 | hp1 | a0004 | c0004 | t0002 | g0233 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00609 | hp2 | a0010 | c0008 | t0003 | g0014 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00621 | hp1 | a0015 | c0029 | t0003 | g0010 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00621 | hp2 | a0006 | c0015 | t0005 | g0235 | EAS | CHS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00642 | hp1 | a0002 | c0001 | t0002 | g0169 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00642 | hp2 | a0019 | c0026 | t0006 | g0070 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00733 | hp1 | a0005 | c0014 | t0001 | g0005 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00733 | hp2 | a0002 | c0001 | t0002 | g0177 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00738 | hp1 | a0004 | c0075 | t0004 | g0266 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00738 | hp2 | a0008 | c0005 | t0001 | g0089 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00741 | hp1 | a0031 | c0056 | t0001 | g0232 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG00741 | hp2 | a0014 | c0016 | t0006 | g0074 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0267 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01069 | hp2 | a0008 | c0005 | t0010 | g0087 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01070 | hp1 | a0039 | c0090 | t0001 | g0116 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01070 | hp2 | a0001 | c0002 | t0010 | g0330 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0306 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01071 | hp2 | a0008 | c0005 | t0001 | g0088 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01074 | hp1 | a0006 | c0015 | t0005 | g0004 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01081 | hp1 | a0003 | c0003 | t0019 | g0360 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01081 | hp2 | a0009 | c0019 | t0011 | g0172 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01099 | hp1 | a0003 | c0013 | t0001 | g0291 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01099 | hp2 | a0009 | c0019 | t0011 | g0193 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01109 | hp1 | a0024 | c0083 | t0001 | g0056 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01109 | hp2 | a0005 | c0034 | t0002 | g0198 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01169 | hp1 | a0002 | c0001 | t0002 | g0092 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01169 | hp2 | a0002 | c0001 | t0006 | g0120 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0279 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01175 | hp2 | a0002 | c0001 | t0002 | g0179 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01192 | hp1 | a0005 | c0062 | t0026 | g0250 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01192 | hp2 | a0002 | c0001 | t0002 | g0184 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01243 | hp1 | a0022 | c0025 | t0001 | g0349 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01243 | hp2 | a0005 | c0034 | t0002 | g0197 | AMR | PUR | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01255 | hp1 | a0006 | c0007 | t0005 | g0303 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0277 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01256 | hp1 | a0005 | c0014 | t0001 | g0315 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01256 | hp2 | a0019 | c0026 | t0006 | g0075 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01257 | hp1 | a0005 | c0014 | t0001 | g0308 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01257 | hp2 | a0009 | c0019 | t0011 | g0003 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01258 | hp1 | a0009 | c0019 | t0011 | g0003 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01258 | hp2 | a0005 | c0014 | t0001 | g0005 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01261 | hp1 | a0014 | c0016 | t0006 | g0069 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01261 | hp2 | a0001 | c0009 | t0001 | g0178 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01346 | hp1 | a0014 | c0016 | t0006 | g0073 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01346 | hp2 | a0005 | c0017 | t0002 | g0076 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0305 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01358 | hp2 | a0004 | c0045 | t0002 | g0231 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01361 | hp1 | a0001 | c0011 | t0008 | g0111 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01361 | hp2 | a0006 | c0007 | t0005 | g0324 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01433 | hp1 | a0005 | c0014 | t0001 | g0304 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0268 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01496 | hp1 | a0018 | c0028 | t0012 | g0259 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01496 | hp2 | a0005 | c0023 | t0018 | g0361 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01515 | hp1 | a0008 | c0005 | t0001 | g0102 | EUR | IBS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01515 | hp2 | a0003 | c0003 | t0010 | g0328 | EUR | IBS | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01884 | hp1 | a0006 | c0007 | t0024 | g0212 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01884 | hp2 | a0023 | c0033 | t0001 | g0338 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01891 | hp1 | a0013 | c0021 | t0004 | g0129 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01891 | hp2 | a0023 | c0033 | t0001 | g0127 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01928 | hp1 | a0047 | c0054 | t0005 | g0236 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01928 | hp2 | a0004 | c0045 | t0002 | g0230 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01952 | hp1 | a0006 | c0007 | t0005 | g0270 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01952 | hp2 | a0001 | c0009 | t0001 | g0188 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01978 | hp1 | a0004 | c0004 | t0002 | g0307 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01978 | hp2 | a0008 | c0005 | t0001 | g0118 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01981 | hp1 | a0003 | c0003 | t0019 | g0273 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01981 | hp2 | a0009 | c0031 | t0001 | g0108 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01993 | hp1 | a0002 | c0001 | t0002 | g0182 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01993 | hp2 | a0006 | c0007 | t0022 | g0054 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02004 | hp1 | a0002 | c0001 | t0002 | g0112 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02004 | hp2 | a0006 | c0007 | t0005 | g0296 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02015 | hp1 | a0009 | c0042 | t0008 | g0106 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02015 | hp2 | a0011 | c0010 | t0001 | g0211 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02040 | hp1 | a0004 | c0018 | t0004 | g0292 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02040 | hp2 | a0002 | c0001 | t0002 | g0190 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02055 | hp1 | a0022 | c0025 | t0001 | g0347 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02055 | hp2 | a0004 | c0073 | t0002 | g0274 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02071 | hp2 | a0009 | c0099 | t0001 | g0146 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02080 | hp1 | a0002 | c0001 | t0002 | g0195 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02080 | hp2 | a0009 | c0044 | t0001 | g0140 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02083 | hp1 | a0002 | c0001 | t0002 | g0082 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0336 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02129 | hp1 | a0011 | c0076 | t0001 | g0206 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02129 | hp2 | a0008 | c0005 | t0001 | g0085 | EAS | KHV | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02145 | hp1 | a0053 | c0104 | t0028 | g0341 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02145 | hp2 | a0004 | c0018 | t0004 | g0224 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02148 | hp1 | a0008 | c0005 | t0001 | g0086 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02148 | hp2 | a0006 | c0007 | t0005 | g0287 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02155 | hp1 | a0011 | c0010 | t0001 | g0209 | EAS | CDX | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02155 | hp2 | a0002 | c0001 | t0002 | g0157 | EAS | CDX | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02257 | hp1 | a0049 | c0064 | t0014 | g0343 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02257 | hp2 | a0055 | c0079 | t0023 | g0194 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02258 | hp1 | a0011 | c0010 | t0001 | g0228 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02258 | hp2 | a0021 | c0032 | t0001 | g0319 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02273 | hp1 | a0004 | c0004 | t0002 | g0297 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02273 | hp2 | a0006 | c0015 | t0005 | g0004 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02280 | hp1 | a0005 | c0067 | t0002 | g0359 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02280 | hp2 | a0003 | c0003 | t0004 | g0337 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02300 | hp1 | a0004 | c0004 | t0002 | g0301 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02300 | hp2 | a0002 | c0001 | t0002 | g0098 | AMR | PEL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02572 | hp1 | a0013 | c0021 | t0004 | g0254 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02572 | hp2 | a0028 | c0038 | t0005 | g0354 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02602 | hp1 | a0002 | c0001 | t0002 | g0154 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02602 | hp2 | a0038 | c0088 | t0002 | g0097 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02615 | hp1 | a0013 | c0021 | t0004 | g0255 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02615 | hp2 | a0011 | c0010 | t0001 | g0265 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02622 | hp1 | a0004 | c0018 | t0004 | g0226 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02622 | hp2 | a0013 | c0021 | t0004 | g0256 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02630 | hp1 | a0012 | c0012 | t0006 | g0058 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02630 | hp2 | a0021 | c0032 | t0001 | g0317 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02647 | hp1 | a0017 | c0022 | t0004 | g0252 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02647 | hp2 | a0001 | c0009 | t0015 | g0124 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02698 | hp1 | a0004 | c0018 | t0004 | g0334 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02698 | hp2 | a0001 | c0002 | t0008 | g0144 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02723 | hp1 | a0048 | c0072 | t0006 | g0352 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02723 | hp2 | a0002 | c0093 | t0004 | g0122 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0327 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02735 | hp2 | a0009 | c0019 | t0002 | g0173 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02738 | hp1 | a0004 | c0074 | t0002 | g0286 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02738 | hp2 | a0013 | c0059 | t0002 | g0067 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02809 | hp1 | a0001 | c0009 | t0015 | g0350 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02809 | hp2 | a0029 | c0046 | t0004 | g0339 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02818 | hp1 | a0009 | c0100 | t0005 | g0318 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02818 | hp2 | a0050 | c0063 | t0012 | g0149 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02886 | hp1 | a0030 | c0047 | t0001 | g0358 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02886 | hp2 | a0040 | c0091 | t0002 | g0189 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02895 | hp1 | a0003 | c0027 | t0002 | g0214 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02895 | hp2 | a0005 | c0061 | t0002 | g0257 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02896 | hp1 | a0012 | c0012 | t0006 | g0062 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02896 | hp2 | a0006 | c0007 | t0005 | g0204 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02897 | hp1 | a0003 | c0027 | t0002 | g0218 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02897 | hp2 | a0012 | c0012 | t0006 | g0061 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02922 | hp1 | a0017 | c0022 | t0004 | g0130 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02922 | hp2 | a0004 | c0050 | t0014 | g0345 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02965 | hp1 | a0036 | c0087 | t0003 | g0033 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02965 | hp2 | a0022 | c0025 | t0001 | g0348 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02970 | hp1 | a0012 | c0012 | t0006 | g0059 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02976 | hp1 | a0003 | c0027 | t0002 | g0215 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02976 | hp2 | a0027 | c0071 | t0001 | g0355 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03017 | hp1 | a0005 | c0017 | t0002 | g0079 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03017 | hp2 | a0004 | c0004 | t0002 | g0333 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03041 | hp1 | a0017 | c0022 | t0004 | g0131 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03041 | hp2 | a0012 | c0012 | t0006 | g0063 | AFR | GWD | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0344 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03098 | hp2 | a0033 | c0058 | t0001 | g0248 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03130 | hp1 | a0026 | c0036 | t0002 | g0202 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03130 | hp2 | a0011 | c0010 | t0013 | g0264 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03139 | hp1 | a0016 | c0095 | t0025 | g0183 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03139 | hp2 | a0003 | c0077 | t0004 | g0356 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03195 | hp1 | a0012 | c0012 | t0006 | g0057 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03195 | hp2 | a0028 | c0038 | t0005 | g0353 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03209 | hp1 | a0023 | c0033 | t0001 | g0126 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03209 | hp2 | a0017 | c0022 | t0004 | g0261 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03225 | hp1 | a0026 | c0036 | t0002 | g0203 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03225 | hp2 | a0018 | c0028 | t0012 | g0260 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03239 | hp1 | a0011 | c0010 | t0001 | g0302 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0275 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03453 | hp1 | a0034 | c0060 | t0014 | g0253 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03453 | hp2 | a0005 | c0103 | t0012 | g0091 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03490 | hp1 | a0002 | c0098 | t0002 | g0147 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03490 | hp2 | a0008 | c0005 | t0001 | g0196 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03491 | hp1 | a0007 | c0041 | t0016 | g0031 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03491 | hp2 | a0003 | c0003 | t0001 | g0329 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03516 | hp1 | a0014 | c0016 | t0006 | g0071 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03516 | hp2 | a0009 | c0092 | t0002 | g0093 | AFR | ESN | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03579 | hp1 | a0001 | c0024 | t0015 | g0321 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03579 | hp2 | a0006 | c0007 | t0005 | g0357 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03654 | hp1 | a0009 | c0031 | t0001 | g0181 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03654 | hp2 | a0051 | c0097 | t0002 | g0186 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03669 | hp1 | a0005 | c0017 | t0002 | g0078 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03669 | hp2 | a0004 | c0004 | t0002 | g0281 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03688 | hp1 | a0001 | c0011 | t0001 | g0114 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03688 | hp2 | a0001 | c0009 | t0001 | g0101 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03704 | hp1 | a0002 | c0001 | t0002 | g0185 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03704 | hp2 | a0005 | c0017 | t0001 | g0081 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03710 | hp1 | a0001 | c0094 | t0008 | g0176 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03710 | hp2 | a0001 | c0009 | t0001 | g0123 | SAS | PJL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03834 | hp1 | a0002 | c0096 | t0002 | g0156 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03834 | hp2 | a0008 | c0005 | t0001 | g0083 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03927 | hp1 | a0010 | c0008 | t0001 | g0077 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03927 | hp2 | a0009 | c0042 | t0008 | g0105 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03942 | hp1 | a0004 | c0004 | t0002 | g0278 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03942 | hp2 | a0001 | c0009 | t0001 | g0244 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG04115 | hp1 | a0004 | c0004 | t0002 | g0325 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG04115 | hp2 | a0002 | c0001 | t0002 | g0175 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG04184 | hp1 | a0007 | c0041 | t0007 | g0030 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG04184 | hp2 | a0003 | c0013 | t0008 | g0246 | SAS | BEB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG04199 | hp1 | a0008 | c0005 | t0001 | g0121 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG04199 | hp2 | a0002 | c0001 | t0002 | g0180 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG04204 | hp1 | a0002 | c0001 | t0002 | g0103 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG04204 | hp2 | a0008 | c0005 | t0001 | g0119 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG04228 | hp1 | a0005 | c0023 | t0001 | g0314 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG04228 | hp2 | a0004 | c0004 | t0002 | g0280 | SAS | STU | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0322 | AFR | YRI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18522 | hp2 | a0003 | c0069 | t0005 | g0219 | AFR | YRI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18612 | hp1 | a0005 | c0017 | t0002 | g0080 | EAS | CHB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18612 | hp2 | a0006 | c0015 | t0002 | g0241 | EAS | CHB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18747 | hp1 | a0005 | c0014 | t0001 | g0289 | EAS | CHB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18747 | hp2 | a0002 | c0020 | t0002 | g0148 | EAS | CHB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18906 | hp1 | a0003 | c0035 | t0004 | g0151 | AFR | YRI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18906 | hp2 | a0004 | c0051 | t0004 | g0342 | AFR | YRI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18939 | hp1 | a0001 | c0009 | t0001 | g0155 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18939 | hp2 | a0002 | c0001 | t0002 | g0158 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18940 | hp1 | a0003 | c0013 | t0001 | g0282 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18940 | hp2 | a0002 | c0001 | t0002 | g0191 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18942 | hp1 | a0015 | c0029 | t0003 | g0024 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18942 | hp2 | a0007 | c0006 | t0017 | g0012 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18943 | hp1 | a0004 | c0004 | t0002 | g0205 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18943 | hp2 | a0001 | c0009 | t0010 | g0107 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18944 | hp1 | a0006 | c0007 | t0005 | g0222 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18944 | hp2 | a0004 | c0004 | t0001 | g0269 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18945 | hp1 | a0001 | c0009 | t0001 | g0160 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18945 | hp2 | a0042 | c0089 | t0009 | g0022 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18947 | hp1 | a0001 | c0011 | t0001 | g0161 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18947 | hp2 | a0007 | c0006 | t0003 | g0052 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18948 | hp1 | a0001 | c0002 | t0008 | g0139 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18948 | hp2 | a0007 | c0006 | t0007 | g0037 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18950 | hp1 | a0002 | c0020 | t0001 | g0145 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18950 | hp2 | a0025 | c0039 | t0003 | g0042 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18952 | hp1 | a0054 | c0080 | t0003 | g0047 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0217 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18953 | hp1 | a0007 | c0006 | t0007 | g0035 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18953 | hp2 | a0003 | c0003 | t0001 | g0229 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18954 | hp1 | a0035 | c0085 | t0003 | g0046 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18954 | hp2 | a0004 | c0004 | t0002 | g0220 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18956 | hp1 | a0010 | c0008 | t0003 | g0034 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18959 | hp1 | a0002 | c0001 | t0002 | g0109 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18961 | hp1 | a0015 | c0040 | t0003 | g0040 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18961 | hp2 | a0004 | c0004 | t0002 | g0223 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18963 | hp1 | a0001 | c0009 | t0010 | g0163 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18963 | hp2 | a0006 | c0007 | t0005 | g0221 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0331 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18964 | hp2 | a0007 | c0006 | t0017 | g0039 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18965 | hp1 | a0020 | c0030 | t0009 | g0029 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18965 | hp2 | a0004 | c0004 | t0002 | g0210 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18966 | hp1 | a0015 | c0040 | t0003 | g0036 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18968 | hp1 | a0003 | c0003 | t0001 | g0239 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18968 | hp2 | a0004 | c0004 | t0002 | g0284 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18971 | hp1 | a0003 | c0013 | t0001 | g0272 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18971 | hp2 | a0004 | c0004 | t0002 | g0293 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18972 | hp1 | a0010 | c0008 | t0003 | g0026 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18972 | hp2 | a0003 | c0068 | t0013 | g0316 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18975 | hp1 | a0020 | c0030 | t0009 | g0049 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18975 | hp2 | a0003 | c0003 | t0001 | g0247 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18977 | hp1 | a0009 | c0044 | t0001 | g0335 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18977 | hp2 | a0003 | c0003 | t0001 | g0332 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18981 | hp1 | a0002 | c0001 | t0002 | g0168 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18981 | hp2 | a0004 | c0004 | t0002 | g0312 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18982 | hp1 | a0002 | c0020 | t0011 | g0132 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18982 | hp2 | a0016 | c0043 | t0009 | g0016 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18983 | hp1 | a0004 | c0004 | t0002 | g0311 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18983 | hp2 | a0006 | c0015 | t0005 | g0237 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18984 | hp1 | a0002 | c0001 | t0002 | g0110 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18984 | hp2 | a0041 | c0102 | t0001 | g0143 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18990 | hp1 | a0007 | c0006 | t0007 | g0006 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18990 | hp2 | a0016 | c0043 | t0009 | g0020 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18992 | hp1 | a0002 | c0001 | t0002 | g0099 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18992 | hp2 | a0001 | c0024 | t0003 | g0008 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18993 | hp1 | a0003 | c0003 | t0001 | g0216 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18993 | hp2 | a0015 | c0029 | t0003 | g0025 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18995 | hp1 | a0016 | c0101 | t0005 | g0066 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18995 | hp2 | a0025 | c0039 | t0003 | g0041 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18999 | hp1 | a0006 | c0007 | t0027 | g0295 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA18999 | hp2 | a0001 | c0002 | t0008 | g0137 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19000 | hp1 | a0007 | c0006 | t0007 | g0051 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19000 | hp2 | a0006 | c0007 | t0005 | g0200 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19001 | hp1 | a0003 | c0003 | t0001 | g0240 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19001 | hp2 | a0002 | c0001 | t0001 | g0165 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19002 | hp1 | a0001 | c0011 | t0008 | g0153 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19002 | hp2 | a0002 | c0001 | t0002 | g0167 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19004 | hp1 | a0003 | c0003 | t0001 | g0208 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19004 | hp2 | a0007 | c0006 | t0007 | g0001 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19005 | hp1 | a0002 | c0001 | t0007 | g0018 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19005 | hp2 | a0001 | c0024 | t0003 | g0009 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19007 | hp1 | a0007 | c0006 | t0007 | g0043 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19007 | hp2 | a0003 | c0003 | t0001 | g0309 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19009 | hp1 | a0002 | c0001 | t0002 | g0100 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19009 | hp2 | a0011 | c0010 | t0001 | g0225 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19010 | hp1 | a0003 | c0013 | t0008 | g0313 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19010 | hp2 | a0010 | c0008 | t0003 | g0027 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19030 | hp1 | a0004 | c0018 | t0004 | g0213 | AFR | LWK | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19030 | hp2 | a0011 | c0010 | t0001 | g0064 | AFR | LWK | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19056 | hp1 | a0001 | c0011 | t0001 | g0162 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19056 | hp2 | a0007 | c0006 | t0007 | g0001 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19058 | hp1 | a0003 | c0055 | t0001 | g0238 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19058 | hp2 | a0037 | c0084 | t0007 | g0038 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19060 | hp1 | a0020 | c0030 | t0009 | g0048 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19060 | hp2 | a0009 | c0031 | t0001 | g0166 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19062 | hp1 | a0001 | c0002 | t0008 | g0136 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19062 | hp2 | a0010 | c0008 | t0021 | g0011 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19063 | hp2 | a0043 | c0048 | t0005 | g0243 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19064 | hp1 | a0002 | c0001 | t0002 | g0113 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19064 | hp2 | a0003 | c0003 | t0003 | g0053 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19065 | hp1 | a0002 | c0001 | t0002 | g0094 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0207 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0283 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19066 | hp2 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19067 | hp1 | a0007 | c0006 | t0016 | g0050 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19067 | hp2 | a0001 | c0011 | t0001 | g0095 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19068 | hp1 | a0010 | c0008 | t0003 | g0017 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19068 | hp2 | a0001 | c0024 | t0001 | g0133 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19074 | hp1 | a0010 | c0008 | t0003 | g0032 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19074 | hp2 | a0001 | c0011 | t0001 | g0164 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19078 | hp1 | a0002 | c0020 | t0002 | g0065 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19078 | hp2 | a0001 | c0002 | t0013 | g0135 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19080 | hp1 | a0003 | c0052 | t0001 | g0234 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19080 | hp2 | a0002 | c0020 | t0002 | g0249 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19082 | hp1 | a0010 | c0008 | t0003 | g0023 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19082 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19084 | hp1 | a0002 | c0001 | t0002 | g0170 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0199 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19087 | hp1 | a0003 | c0003 | t0013 | g0201 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19087 | hp2 | a0002 | c0001 | t0002 | g0096 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19090 | hp1 | a0010 | c0008 | t0007 | g0021 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19090 | hp2 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19240 | hp1 | a0012 | c0012 | t0006 | g0060 | AFR | YRI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA19240 | hp2 | a0014 | c0016 | t0006 | g0072 | AFR | YRI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA20129 | hp1 | a0011 | c0010 | t0001 | g0227 | AFR | ASW | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA20129 | hp2 | a0005 | c0037 | t0004 | g0152 | AFR | ASW | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA20752 | hp1 | a0008 | c0005 | t0001 | g0090 | EUR | TSI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA20752 | hp2 | a0002 | c0001 | t0002 | g0125 | EUR | TSI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0298 | EUR | TSI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0192 | EUR | TSI | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA20905 | hp1 | a0002 | c0001 | t0002 | g0174 | SAS | GIH | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA20905 | hp2 | a0005 | c0066 | t0002 | g0251 | SAS | GIH | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01123 | hp1 | a0002 | c0001 | t0002 | g0171 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG01123 | hp2 | a0021 | c0032 | t0001 | g0320 | AMR | CLM | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02109 | hp1 | a0002 | c0001 | t0002 | g0159 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02109 | hp2 | a0044 | c0065 | t0005 | g0326 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02486 | hp1 | a0024 | c0082 | t0004 | g0055 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02486 | hp2 | a0056 | c0078 | t0001 | g0294 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02559 | hp1 | a0005 | c0037 | t0004 | g0271 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG02559 | hp2 | a0003 | c0035 | t0004 | g0150 | AFR | ACB | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03471 | hp1 | a0052 | c0057 | t0014 | g0346 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG03471 | hp2 | a0029 | c0046 | t0004 | g0340 | AFR | MSL | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0323 | AFR | USA | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| HG06807 | hp2 | a0011 | c0010 | t0001 | g0263 | AFR | USA | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA20300 | hp1 | a0001 | c0009 | t0002 | g0117 | AFR | USA | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA20300 | hp2 | a0018 | c0028 | t0012 | g0258 | AFR | USA | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA21309 | hp1 | a0027 | c0070 | t0002 | g0351 | AFR | LWK | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| NA21309 | hp2 | a0045 | c0049 | t0002 | g0242 | AFR | LWK | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| homoSapiens_chm13v2 | hp1 | a0019 | c0026 | t0006 | g0068 | REF | REF | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| homoSapiens_grch38 | hp1 | a0032 | c0081 | t0002 | g0262 | REF | REF | TNC_chr9_115014575_115123157 | TNC | chr9 | 115014575 | 115123157 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:115021264
|
C | T | 1 | a0040 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.6499G>A | p.Val2167Ile | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 6811/8500 | 6499/6606 | 2167/2201 | chr9 | 115021264 | ||
| chr9:115023986
|
T | C | 1 | a0053 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.6482A>G | p.Asn2161Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/28 | 6794/8500 | 6482/6606 | 2161/2201 | chr9 | 115023986 | ||
| chr9:115024090
|
G | C | 1 | a0035 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.6378C>G | p.Asp2126Glu | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/28 | 6690/8500 | 6378/6606 | 2126/2201 | chr9 | 115024090 | ||
| chr9:115030304
|
C | G | 37 | a0001a0003a0005others(34): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
missense_variant | MODERATE | c.6022G>C | p.Glu2008Gln | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/28 | 6334/8500 | 6022/6606 | 2008/2201 | chr9 | 115030304 | ||
| chr9:115036139
|
C | G | 1 | a0021 | 3 | HG01123.hp2 HG02258.hp2 HG02630.hp2 |
missense_variant | MODERATE | c.5615G>C | p.Gly1872Ala | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/28 | 5927/8500 | 5615/6606 | 1872/2201 | chr9 | 115036139 | ||
| chr9:115038284
|
A | C | 1 | a0047 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.5489T>G | p.Val1830Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/28 | 5801/8500 | 5489/6606 | 1830/2201 | chr9 | 115038284 | ||
| chr9:115040992
|
C | T | 8 | a0006a0016a0020others(5): Show | 31 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(28): Show |
missense_variant | MODERATE | c.5341G>A | p.Ala1781Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/28 | 5653/8500 | 5341/6606 | 1781/2201 | chr9 | 115040992 | ||
| chr9:115046442
|
C | T | 1 | a0019 | 3 | HG00642.hp2 HG01256.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.5093G>A | p.Arg1698Gln | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/28 | 5405/8500 | 5093/6606 | 1698/2201 | chr9 | 115046442 | ||
| chr9:115046506
|
T | A | 36 | a0001a0003a0006others(33): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
missense_variant | MODERATE | c.5029A>T | p.Ile1677Leu | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/28 | 5341/8500 | 5029/6606 | 1677/2201 | chr9 | 115046506 | ||
| chr9:115057260
|
C | T | 1 | a0039 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.4472G>A | p.Arg1491Gln | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/28 | 4784/8500 | 4472/6606 | 1491/2201 | chr9 | 115057260 | ||
| chr9:115059808
|
C | A | 1 | a0041 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.4228G>T | p.Ala1410Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/28 | 4540/8500 | 4228/6606 | 1410/2201 | chr9 | 115059808 | ||
| chr9:115063817
|
G | T | 1 | a0045 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.3739C>A | p.Leu1247Ile | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/28 | 4051/8500 | 3739/6606 | 1247/2201 | chr9 | 115063817 | ||
| chr9:115064759
|
G | T | 1 | a0026 | 2 | HG03130.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.3375C>A | p.Ser1125Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 11/28 | 3687/8500 | 3375/6606 | 1125/2201 | chr9 | 115064759 | ||
| chr9:115064781
|
C | T | 1 | a0017 | 4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
missense_variant | MODERATE | c.3353G>A | p.Arg1118Gln | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 11/28 | 3665/8500 | 3353/6606 | 1118/2201 | chr9 | 115064781 | ||
| chr9:115073620
|
C | T | 11 | a0008a0011a0022others(8): Show | 39 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(36): Show |
missense_variant | MODERATE | c.3197G>A | p.Arg1066His | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/28 | 3509/8500 | 3197/6606 | 1066/2201 | chr9 | 115073620 | ||
| chr9:115073770
|
C | G | 1 | a0043 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.3047G>C | p.Arg1016Pro | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/28 | 3359/8500 | 3047/6606 | 1016/2201 | chr9 | 115073770 | ||
| chr9:115077997
|
T | C | 3 | a0027a0028a0048 | 5 | HG02572.hp2 HG02723.hp1 HG02976.hp2 others(2): Show |
missense_variant | MODERATE | c.2620A>G | p.Ile874Val | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2932/8500 | 2620/6606 | 874/2201 | chr9 | 115077997 | ||
| chr9:115078036
|
C | G | 1 | a0037 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.2581G>C | p.Gly861Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2893/8500 | 2581/6606 | 861/2201 | chr9 | 115078036 | ||
| chr9:115078069
|
C | G | 1 | a0042 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.2548G>C | p.Asp850His | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2860/8500 | 2548/6606 | 850/2201 | chr9 | 115078069 | ||
| chr9:115078080
|
C | T | 1 | a0038 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.2537G>A | p.Arg846His | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2849/8500 | 2537/6606 | 846/2201 | chr9 | 115078080 | ||
| chr9:115082732
|
T | C | 3 | a0017a0049a0050 | 6 | HG02257.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
missense_variant | MODERATE | c.2207A>G | p.Asp736Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/28 | 2519/8500 | 2207/6606 | 736/2201 | chr9 | 115082732 | ||
| chr9:115084301
|
T | C | 28 | a0003a0004a0005others(25): Show | 166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
missense_variant | MODERATE | c.2039A>G | p.Gln680Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/28 | 2351/8500 | 2039/6606 | 680/2201 | chr9 | 115084301 | ||
| chr9:115084460
|
T | C | 1 | a0051 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.1880A>G | p.Lys627Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/28 | 2192/8500 | 1880/6606 | 627/2201 | chr9 | 115084460 | ||
| chr9:115085918
|
C | T | 9 | a0007a0010a0015others(6): Show | 43 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(40): Show |
missense_variant | MODERATE | c.1813G>A | p.Val605Ile | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 2125/8500 | 1813/6606 | 605/2201 | chr9 | 115085918 | ||
| chr9:115086115
|
T | C | 48 | a0001a0002a0003others(45): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
missense_variant | MODERATE | c.1616A>G | p.Gln539Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1928/8500 | 1616/6606 | 539/2201 | chr9 | 115086115 | ||
| chr9:115086223
|
C | T | 2 | a0029a0053 | 3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.1508G>A | p.Arg503Lys | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1820/8500 | 1508/6606 | 503/2201 | chr9 | 115086223 | ||
| chr9:115086389
|
G | C | 1 | a0031 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1342C>G | p.Arg448Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1654/8500 | 1342/6606 | 448/2201 | chr9 | 115086389 | ||
| chr9:115086409
|
T | C | 1 | a0052 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1322A>G | p.Asn441Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1634/8500 | 1322/6606 | 441/2201 | chr9 | 115086409 | ||
| chr9:115086950
|
C | T | 1 | a0022 | 3 | HG01243.hp1 HG02055.hp1 HG02965.hp2 |
missense_variant | MODERATE | c.781G>A | p.Gly261Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1093/8500 | 781/6606 | 261/2201 | chr9 | 115086950 | ||
| chr9:115087094
|
C | T | 2 | a0029a0053 | 3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.637G>A | p.Gly213Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 949/8500 | 637/6606 | 213/2201 | chr9 | 115087094 | ||
| chr9:115090576
|
A | G | 1 | a0054 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.443T>C | p.Leu148Pro | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 755/8500 | 443/6606 | 148/2201 | chr9 | 115090576 | ||
| chr9:115090585
|
C | A | 1 | a0023 | 3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
missense_variant | MODERATE | c.434G>T | p.Gly145Val | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 746/8500 | 434/6606 | 145/2201 | chr9 | 115090585 | ||
| chr9:115090676
|
C | T | 1 | a0055 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.343G>A | p.Ala115Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 655/8500 | 343/6606 | 115/2201 | chr9 | 115090676 | ||
| chr9:115090694
|
G | A | 1 | a0056 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.325C>T | p.Arg109Trp | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 637/8500 | 325/6606 | 109/2201 | chr9 | 115090694 | ||
| chr9:115090921
|
C | T | 1 | a0030 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.98G>A | p.Arg33Gln | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 410/8500 | 98/6606 | 33/2201 | chr9 | 115090921 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:115029385
|
C | T | 5 | a0005c0014a0009c0031a0009c0044others(2): Show | 24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
synonymous_variant | LOW | c.6144G>A | p.Gly2048Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/28 | 6456/8500 | 6144/6606 | 2048/2201 | chr9 | 115029385 | ||
| chr9:115029430
|
G | A | 4 | a0005c0037a0005c0066a0013c0021others(1): Show | 9 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
synonymous_variant | LOW | c.6099C>T | p.Arg2033Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/28 | 6411/8500 | 6099/6606 | 2033/2201 | chr9 | 115029430 | ||
| chr9:115029451
|
G | A | 1 | a0001c0094 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.6078C>T | p.Phe2026Phe | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/28 | 6390/8500 | 6078/6606 | 2026/2201 | chr9 | 115029451 | ||
| chr9:115030299
|
C | G | 1 | a0005c0062 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.6027G>C | p.Ala2009Ala | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/28 | 6339/8500 | 6027/6606 | 2009/2201 | chr9 | 115030299 | ||
| chr9:115030320
|
C | T | 1 | a0017c0022 | 4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
synonymous_variant | LOW | c.6006G>A | p.Leu2002Leu | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/28 | 6318/8500 | 6006/6606 | 2002/2201 | chr9 | 115030320 | ||
| chr9:115035246
|
G | T | 2 | a0003c0027a0026c0036 | 5 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(2): Show |
synonymous_variant | LOW | c.5745C>A | p.Thr1915Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/28 | 6057/8500 | 5745/6606 | 1915/2201 | chr9 | 115035246 | ||
| chr9:115035318
|
T | C | 12 | a0001c0002a0001c0011a0001c0094others(9): Show | 56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
synonymous_variant | LOW | c.5673A>G | p.Arg1891Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/28 | 5985/8500 | 5673/6606 | 1891/2201 | chr9 | 115035318 | ||
| chr9:115038268
|
G | C | 1 | a0005c0062 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.5505C>G | p.Gly1835Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/28 | 5817/8500 | 5505/6606 | 1835/2201 | chr9 | 115038268 | ||
| chr9:115041017
|
G | A | 1 | a0003c0068 | 1 | NA18972.hp2 | synonymous_variant | LOW | c.5316C>T | p.Gly1772Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/28 | 5628/8500 | 5316/6606 | 1772/2201 | chr9 | 115041017 | ||
| chr9:115042265
|
T | C | 36 | a0002c0093a0003c0027a0003c0069others(33): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
synonymous_variant | LOW | c.5202A>G | p.Thr1734Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/28 | 5514/8500 | 5202/6606 | 1734/2201 | chr9 | 115042265 | ||
| chr9:115042274
|
C | T | 2 | a0005c0037a0013c0021 | 6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
synonymous_variant | LOW | c.5193G>A | p.Arg1731Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/28 | 5505/8500 | 5193/6606 | 1731/2201 | chr9 | 115042274 | ||
| chr9:115042292
|
C | T | 1 | a0011c0076 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.5175G>A | p.Ser1725Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/28 | 5487/8500 | 5175/6606 | 1725/2201 | chr9 | 115042292 | ||
| chr9:115048372
|
G | A | 1 | a0016c0095 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.4740C>T | p.Thr1580Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/28 | 5052/8500 | 4740/6606 | 1580/2201 | chr9 | 115048372 | ||
| chr9:115057157
|
C | T | 5 | a0005c0017a0005c0066a0009c0019others(2): Show | 13 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(10): Show |
synonymous_variant | LOW | c.4575G>A | p.Thr1525Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/28 | 4887/8500 | 4575/6606 | 1525/2201 | chr9 | 115057157 | ||
| chr9:115059854
|
C | T | 1 | a0004c0073 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.4182G>A | p.Thr1394Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/28 | 4494/8500 | 4182/6606 | 1394/2201 | chr9 | 115059854 | ||
| chr9:115073652
|
G | A | 6 | a0005c0014a0007c0041a0009c0031others(3): Show | 26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
synonymous_variant | LOW | c.3165C>T | p.Ala1055Ala | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/28 | 3477/8500 | 3165/6606 | 1055/2201 | chr9 | 115073652 | ||
| chr9:115077944
|
T | G | 1 | a0002c0096 | 1 | HG03834.hp1 | splice_region_variant&synonymous_variant | LOW | c.2673A>C | p.Thr891Thr | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2985/8500 | 2673/6606 | 891/2201 | chr9 | 115077944 | ||
| chr9:115078055
|
G | A | 3 | a0004c0073a0004c0074a0004c0075 | 3 | HG00738.hp1 HG02055.hp2 HG02738.hp1 |
synonymous_variant | LOW | c.2562C>T | p.Asp854Asp | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2874/8500 | 2562/6606 | 854/2201 | chr9 | 115078055 | ||
| chr9:115078160
|
G | A | 1 | a0003c0055 | 1 | NA19058.hp1 | synonymous_variant | LOW | c.2457C>T | p.Ala819Ala | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/28 | 2769/8500 | 2457/6606 | 819/2201 | chr9 | 115078160 | ||
| chr9:115081787
|
T | G | 7 | a0003c0035a0005c0061a0005c0062others(4): Show | 13 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
synonymous_variant | LOW | c.2389A>C | p.Arg797Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/28 | 2701/8500 | 2389/6606 | 797/2201 | chr9 | 115081787 | ||
| chr9:115081803
|
C | T | 2 | a0002c0098a0009c0099 | 2 | HG02071.hp2 HG03490.hp1 |
synonymous_variant | LOW | c.2373G>A | p.Arg791Arg | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/28 | 2685/8500 | 2373/6606 | 791/2201 | chr9 | 115081803 | ||
| chr9:115081860
|
A | T | 1 | a0038c0088 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.2316T>A | p.Gly772Gly | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/28 | 2628/8500 | 2316/6606 | 772/2201 | chr9 | 115081860 | ||
| chr9:115084291
|
C | T | 41 | a0001c0009a0001c0011a0001c0094others(38): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
synonymous_variant | LOW | c.2049G>A | p.Glu683Glu | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/28 | 2361/8500 | 2049/6606 | 683/2201 | chr9 | 115084291 | ||
| chr9:115085922
|
T | C | 10 | a0001c0002a0001c0024a0002c0020others(7): Show | 45 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(42): Show |
synonymous_variant | LOW | c.1809A>G | p.Gln603Gln | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 2121/8500 | 1809/6606 | 603/2201 | chr9 | 115085922 | ||
| chr9:115086264
|
G | A | 1 | a0011c0076 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.1467C>T | p.Asp489Asp | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1779/8500 | 1467/6606 | 489/2201 | chr9 | 115086264 | ||
| chr9:115086786
|
G | A | 1 | a0003c0077 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.945C>T | p.Cys315Cys | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1257/8500 | 945/6606 | 315/2201 | chr9 | 115086786 | ||
| chr9:115087035
|
T | C | 56 | a0003c0003a0003c0013a0003c0027others(53): Show | 166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
synonymous_variant | LOW | c.696A>G | p.Val232Val | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/28 | 1008/8500 | 696/6606 | 232/2201 | chr9 | 115087035 | ||
| chr9:115090743
|
C | T | 54 | a0003c0003a0003c0013a0003c0027others(51): Show | 163 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(160): Show |
synonymous_variant | LOW | c.276G>A | p.Val92Val | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 588/8500 | 276/6606 | 92/2201 | chr9 | 115090743 | ||
| chr9:115090824
|
C | T | 13 | a0003c0052a0003c0055a0004c0050others(10): Show | 20 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(17): Show |
synonymous_variant | LOW | c.195G>A | p.Ser65Ser | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 507/8500 | 195/6606 | 65/2201 | chr9 | 115090824 | ||
| chr9:115090863
|
G | A | 2 | a0029c0046a0053c0104 | 3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.156C>T | p.His52His | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 468/8500 | 156/6606 | 52/2201 | chr9 | 115090863 | ||
| chr9:115090932
|
G | A | 1 | a0053c0104 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.87C>T | p.Ile29Ile | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 399/8500 | 87/6606 | 29/2201 | chr9 | 115090932 | ||
| chr9:115090944
|
G | C | 1 | a0023c0033 | 3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.75C>G | p.Leu25Leu | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 387/8500 | 75/6606 | 25/2201 | chr9 | 115090944 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:115019701
|
C | T | 1 | a0005c0062t0026 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1456G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 1456 | chr9 | 115019701 | |||||
| chr9:115019916
|
C | A | 1 | a0005c0062t0026 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1241G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 1241 | chr9 | 115019916 | |||||
| chr9:115019982
|
C | T | 21 | a0003c0069t0005a0005c0062t0026a0005c0103t0012others(18): Show | 39 | HG00621.hp2 HG01074.hp1 HG01192.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1175G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 1175 | chr9 | 115019982 | |||||
| chr9:115020084
|
A | G | 5 | a0001c0002t0008a0001c0011t0008a0001c0094t0008others(2): Show | 11 | HG01361.hp1 HG02015.hp1 HG02698.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1073T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 1073 | chr9 | 115020084 | |||||
| chr9:115020179
|
G | A | 7 | a0001c0009t0015a0001c0024t0015a0004c0050t0014others(4): Show | 8 | HG02145.hp1 HG02257.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*978C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 978 | chr9 | 115020179 | |||||
| chr9:115020188
|
G | A | 2 | a0005c0023t0018a0046c0053t0018 | 2 | HG00323.hp1 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*969C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 969 | chr9 | 115020188 | |||||
| chr9:115020203
|
C | G | 106 | a0001c0002t0001a0001c0002t0003a0001c0002t0008others(103): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*954G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 954 | chr9 | 115020203 | |||||
| chr9:115020212
|
A | AT | 67 | a0001c0002t0001a0001c0002t0003a0001c0002t0008others(64): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*944dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 944 | chr9 | 115020212 | |||||
| chr9:115020212
|
A | ATT | 6 | a0001c0002t0013a0001c0009t0015a0001c0024t0015others(3): Show | 7 | HG02647.hp2 HG02809.hp1 HG03130.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*943_*944dupAA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 944 | chr9 | 115020212 | |||||
| chr9:115020212
|
AT | A | 4 | a0002c0020t0011a0006c0007t0027a0007c0006t0017others(1): Show | 8 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*944delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 944 | chr9 | 115020212 | |||||
| chr9:115020557
|
T | A | 1 | a0003c0003t0019 | 2 | HG01081.hp1 HG01981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*600A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 600 | chr9 | 115020557 | |||||
| chr9:115020557
|
T | TA | 86 | a0001c0002t0001a0001c0002t0003a0001c0002t0008others(83): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*599dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 599 | chr9 | 115020557 | |||||
| chr9:115020612
|
T | C | 2 | a0001c0009t0015a0001c0024t0015 | 3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*545A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 545 | chr9 | 115020612 | |||||
| chr9:115020809
|
C | T | 1 | a0006c0007t0024 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*348G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 348 | chr9 | 115020809 | |||||
| chr9:115021017
|
C | T | 1 | a0055c0079t0023 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*140G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 28/28 | 140 | chr9 | 115021017 | |||||
| chr9:115091051
|
G | A | 1 | a0053c0104t0028 | 1 | HG02145.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/28 | 33 | chr9 | 115091051 | |||||
| chr9:115118057
|
C | T | 1 | a0006c0007t0022 | 1 | HG01993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-212G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/28 | 27039 | chr9 | 115118057 | |||||
| chr9:115118070
|
T | C | 24 | a0001c0002t0003a0001c0024t0003a0002c0001t0007others(21): Show | 50 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
5_prime_UTR_variant | MODIFIER | c.-225A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/28 | 27052 | chr9 | 115118070 | |||||
| chr9:115118078
|
A | C | 24 | a0001c0002t0003a0001c0024t0003a0002c0001t0007others(21): Show | 50 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
5_prime_UTR_variant | MODIFIER | c.-233T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/28 | 27060 | chr9 | 115118078 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:115021272
|
TA | T | 58 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(55): Show |
splice_region_variant&intron_variant | LOW | c.6496-6delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115021272 | ||||||
| chr9:115021283
|
A | AG | 3 | a0021c0032t0001g0317a0021c0032t0001g0319a0021c0032t0001g0320 | 3 | HG01123.hp2 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.6496-17_6496-16ins others(1): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115021283 | ||||||
| chr9:115021333
|
C | T | 1 | a0001c0011t0001g0161 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.6496-66G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115021333 | ||||||
| chr9:115021705
|
G | T | 60 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.6496-438C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115021705 | ||||||
| chr9:115021911
|
G | C | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6496-644C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115021911 | ||||||
| chr9:115022137
|
T | C | 15 | a0002c0001t0002g0094a0002c0001t0002g0096a0002c0001t0002g0099others(12): Show | 15 | HG00408.hp2 HG01358.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.6496-870A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022137 | ||||||
| chr9:115022194
|
G | T | 1 | a0002c0001t0002g0094 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.6496-927C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022194 | ||||||
| chr9:115022195
|
C | G | 1 | a0013c0021t0004g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.6496-928G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022195 | ||||||
| chr9:115022306
|
T | C | 8 | a0005c0037t0004g0152a0005c0037t0004g0271a0013c0021t0004g0129others(5): Show | 8 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.6496-1039A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022306 | ||||||
| chr9:115022442
|
A | C | 35 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(32): Show | 36 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.6496-1175T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022442 | ||||||
| chr9:115022752
|
G | T | 3 | a0003c0035t0004g0150a0003c0035t0004g0151a0003c0077t0004g0356 | 3 | HG02559.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6495+1221C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022752 | ||||||
| chr9:115022769
|
C | G | 2 | a0034c0060t0014g0253a0049c0064t0014g0343 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.6495+1204G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022769 | ||||||
| chr9:115022769
|
C | T | 60 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.6495+1204G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022769 | ||||||
| chr9:115022776
|
C | T | 13 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(10): Show | 13 | HG00408.hp1 HG00738.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.6495+1197G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022776 | ||||||
| chr9:115022874
|
G | A | 35 | a0008c0005t0001g0083a0008c0005t0001g0084a0008c0005t0001g0085others(32): Show | 35 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.6495+1099C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022874 | ||||||
| chr9:115022901
|
A | G | 1 | a0053c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6495+1072T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115022901 | ||||||
| chr9:115023005
|
C | G | 4 | a0003c0069t0005g0219a0006c0007t0005g0357a0028c0038t0005g0353others(1): Show | 4 | HG02572.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.6495+968G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023005 | ||||||
| chr9:115023037
|
C | CA | 127 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(124): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.6495+935dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023037 | ||||||
| chr9:115023037
|
C | CAA | 12 | a0001c0009t0015g0124a0001c0024t0015g0321a0002c0020t0002g0065others(9): Show | 12 | HG00597.hp2 HG02572.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.6495+934_6495+935d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023037 | ||||||
| chr9:115023037
|
CA | C | 8 | a0001c0009t0001g0101a0003c0003t0019g0273a0004c0004t0002g0223others(5): Show | 8 | HG01192.hp1 HG01981.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6495+935delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023037 | ||||||
| chr9:115023054
|
T | A | 1 | a0025c0039t0003g0042 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.6495+919A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023054 | ||||||
| chr9:115023138
|
A | G | 24 | a0001c0009t0002g0117a0003c0027t0002g0214a0003c0027t0002g0215others(21): Show | 25 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.6495+835T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023138 | ||||||
| chr9:115023144
|
C | T | 23 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(20): Show | 24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6495+829G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023144 | ||||||
| chr9:115023345
|
G | A | 1 | a0004c0004t0002g0312 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.6495+628C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023345 | ||||||
| chr9:115023378
|
G | A | 2 | a0044c0065t0005g0326a0055c0079t0023g0194 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.6495+595C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023378 | ||||||
| chr9:115023476
|
G | A | 33 | a0001c0009t0002g0117a0003c0027t0002g0214a0003c0027t0002g0215others(30): Show | 34 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.6495+497C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023476 | ||||||
| chr9:115023655
|
A | T | 1 | a0012c0012t0006g0058 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6495+318T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023655 | ||||||
| chr9:115023703
|
G | C | 1 | a0012c0012t0006g0058 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6495+270C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023703 | ||||||
| chr9:115023729
|
G | A | 1 | a0005c0034t0002g0197 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6495+244C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023729 | ||||||
| chr9:115023837
|
T | C | 1 | a0002c0001t0002g0184 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.6495+136A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 27/27 | chr9 | 115023837 | ||||||
| chr9:115024229
|
G | A | 17 | a0002c0001t0006g0120a0012c0012t0006g0057a0012c0012t0006g0058others(14): Show | 17 | HG00642.hp2 HG00741.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.6332-93C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024229 | ||||||
| chr9:115024462
|
T | C | 21 | a0002c0001t0006g0120a0009c0100t0005g0318a0012c0012t0006g0057others(18): Show | 21 | HG00642.hp2 HG00741.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.6332-326A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024462 | ||||||
| chr9:115024472
|
C | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6332-336G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024472 | ||||||
| chr9:115024481
|
T | G | 8 | a0005c0037t0004g0152a0005c0037t0004g0271a0013c0021t0004g0129others(5): Show | 8 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.6332-345A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024481 | ||||||
| chr9:115024485
|
T | A | 1 | a0002c0001t0002g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6332-349A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024485 | ||||||
| chr9:115024671
|
T | C | 1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6332-535A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024671 | ||||||
| chr9:115024767
|
G | A | 25 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(22): Show | 26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.6332-631C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024767 | ||||||
| chr9:115024855
|
A | T | 6 | a0005c0037t0004g0152a0005c0037t0004g0271a0013c0021t0004g0129others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.6332-719T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024855 | ||||||
| chr9:115024894
|
A | C | 225 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.6332-758T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024894 | ||||||
| chr9:115024995
|
C | T | 3 | a0004c0051t0004g0342a0034c0060t0014g0253a0049c0064t0014g0343 | 3 | HG02257.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6332-859G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115024995 | ||||||
| chr9:115025055
|
G | A | 26 | a0001c0009t0002g0117a0003c0027t0002g0214a0003c0027t0002g0215others(23): Show | 27 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.6332-919C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025055 | ||||||
| chr9:115025101
|
G | A | 4 | a0018c0028t0012g0258a0018c0028t0012g0259a0018c0028t0012g0260others(1): Show | 4 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.6332-965C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025101 | ||||||
| chr9:115025168
|
G | T | 2 | a0030c0047t0001g0358a0033c0058t0001g0248 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6332-1032C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025168 | ||||||
| chr9:115025387
|
C | CT | 128 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(125): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.6331+1146dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025387 | ||||||
| chr9:115025459
|
C | T | 2 | a0002c0001t0002g0157a0002c0001t0002g0170 | 2 | HG02155.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.6331+1075G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025459 | ||||||
| chr9:115025572
|
T | C | 360 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(357): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.6331+962A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025572 | ||||||
| chr9:115025680
|
T | C | 1 | a0008c0005t0001g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.6331+854A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025680 | ||||||
| chr9:115025739
|
G | A | 23 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(20): Show | 24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6331+795C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025739 | ||||||
| chr9:115025753
|
A | G | 2 | a0012c0012t0006g0060a0014c0016t0006g0071 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.6331+781T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025753 | ||||||
| chr9:115025890
|
G | C | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6331+644C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025890 | ||||||
| chr9:115025993
|
A | G | 1 | a0046c0053t0018g0245 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.6331+541T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115025993 | ||||||
| chr9:115026135
|
G | A | 3 | a0009c0100t0005g0318a0044c0065t0005g0326a0055c0079t0023g0194 | 3 | HG02109.hp2 HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.6331+399C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115026135 | ||||||
| chr9:115026149
|
C | G | 4 | a0005c0034t0002g0197a0005c0034t0002g0198a0005c0067t0002g0359others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.6331+385G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115026149 | ||||||
| chr9:115026172
|
A | T | 1 | a0003c0003t0013g0201 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.6331+362T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115026172 | ||||||
| chr9:115026260
|
G | C | 1 | a0009c0019t0011g0003 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.6331+274C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115026260 | ||||||
| chr9:115026376
|
G | A | 23 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(20): Show | 24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6331+158C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 26/27 | chr9 | 115026376 | ||||||
| chr9:115026706
|
C | T | 2 | a0002c0020t0002g0065a0002c0020t0002g0249 | 2 | NA19078.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.6170-11G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115026706 | ||||||
| chr9:115026723
|
G | A | 11 | a0001c0002t0008g0136a0001c0002t0008g0137a0001c0002t0008g0139others(8): Show | 11 | HG01361.hp1 HG02015.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.6170-28C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115026723 | ||||||
| chr9:115026770
|
C | T | 23 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(20): Show | 24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6170-75G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115026770 | ||||||
| chr9:115026860
|
A | G | 1 | a0043c0048t0005g0243 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.6170-165T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115026860 | ||||||
| chr9:115027006
|
G | A | 2 | a0002c0020t0001g0145a0004c0004t0001g0269 | 2 | NA18944.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.6170-311C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027006 | ||||||
| chr9:115027024
|
G | A | 1 | a0001c0002t0001g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6170-329C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027024 | ||||||
| chr9:115027024
|
G | T | 4 | a0002c0001t0002g0171a0002c0001t0002g0177a0002c0001t0002g0179others(1): Show | 4 | HG00733.hp2 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.6170-329C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027024 | ||||||
| chr9:115027118
|
A | AAAG | 33 | a0001c0009t0002g0117a0003c0027t0002g0214a0003c0027t0002g0215others(30): Show | 34 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.6170-424_6170-423i others(5): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027118 | ||||||
| chr9:115027119
|
A | AAG | 323 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.6170-425_6170-424i others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027119 | ||||||
| chr9:115027120
|
A | AG | 3 | a0003c0035t0004g0150a0003c0035t0004g0151a0003c0077t0004g0356 | 3 | HG02559.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6170-426_6170-425i others(3): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027120 | ||||||
| chr9:115027293
|
C | G | 14 | a0001c0002t0001g0138a0001c0002t0001g0141a0001c0002t0001g0142others(11): Show | 14 | HG00597.hp1 NA18940.hp1 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.6170-598G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027293 | ||||||
| chr9:115027311
|
C | T | 3 | a0003c0035t0004g0150a0003c0035t0004g0151a0003c0077t0004g0356 | 3 | HG02559.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6170-616G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027311 | ||||||
| chr9:115027319
|
G | GTGGC | 23 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(20): Show | 24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6170-628_6170-625d others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027319 | ||||||
| chr9:115027344
|
C | T | 2 | a0005c0017t0002g0079a0005c0066t0002g0251 | 2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.6170-649G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027344 | ||||||
| chr9:115027365
|
G | A | 2 | a0005c0017t0002g0080a0055c0079t0023g0194 | 2 | HG02257.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.6170-670C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027365 | ||||||
| chr9:115027421
|
C | G | 4 | a0017c0022t0004g0130a0017c0022t0004g0131a0017c0022t0004g0252others(1): Show | 4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.6170-726G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027421 | ||||||
| chr9:115027475
|
A | G | 23 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(20): Show | 24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6170-780T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027475 | ||||||
| chr9:115027525
|
G | A | 1 | a0027c0070t0002g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6170-830C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027525 | ||||||
| chr9:115027704
|
G | T | 1 | a0034c0060t0014g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6170-1009C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115027704 | ||||||
| chr9:115028139
|
T | C | 6 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.6169+1221A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028139 | ||||||
| chr9:115028323
|
C | T | 29 | a0001c0009t0002g0117a0003c0027t0002g0214a0003c0027t0002g0215others(26): Show | 30 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.6169+1037G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028323 | ||||||
| chr9:115028396
|
G | A | 4 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(1): Show | 4 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.6169+964C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028396 | ||||||
| chr9:115028423
|
A | G | 1 | a0002c0001t0002g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.6169+937T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028423 | ||||||
| chr9:115028463
|
G | T | 1 | a0050c0063t0012g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6169+897C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028463 | ||||||
| chr9:115028623
|
C | T | 2 | a0005c0017t0002g0076a0045c0049t0002g0242 | 2 | HG01346.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.6169+737G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028623 | ||||||
| chr9:115028646
|
A | C | 52 | a0002c0001t0001g0165a0002c0001t0002g0002a0002c0001t0002g0082others(49): Show | 54 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.6169+714T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028646 | ||||||
| chr9:115028650
|
C | T | 2 | a0001c0002t0001g0306a0001c0002t0010g0330 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.6169+710G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028650 | ||||||
| chr9:115028771
|
T | C | 1 | a0007c0006t0007g0035 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.6169+589A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028771 | ||||||
| chr9:115028874
|
C | T | 23 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(20): Show | 24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.6169+486G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028874 | ||||||
| chr9:115028890
|
C | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6169+470G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028890 | ||||||
| chr9:115028924
|
G | GA | 25 | a0002c0001t0002g0094a0002c0001t0002g0103a0002c0001t0002g0157others(22): Show | 26 | HG00609.hp1 HG00733.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.6169+435dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028924
|
G | GAA | 13 | a0002c0001t0002g0082a0002c0001t0002g0179a0002c0001t0002g0190others(10): Show | 13 | HG01175.hp2 HG01978.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.6169+434_6169+435d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028924
|
GA | G | 18 | a0002c0001t0001g0104a0002c0001t0002g0099a0002c0001t0002g0109others(15): Show | 18 | HG00738.hp1 HG01192.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.6169+435delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028924
|
GAAAAAAA others(3): Show |
G | 7 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(4): Show | 7 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.6169+426_6169+435d others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028924
|
GAAAAAAA others(4): Show |
G | 70 | a0001c0009t0001g0101a0001c0009t0001g0155a0001c0009t0001g0160others(67): Show | 70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.6169+425_6169+435d others(13): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028924
|
GAAAAAAA others(5): Show |
G | 7 | a0001c0002t0001g0142a0003c0003t0001g0247a0003c0003t0001g0331others(4): Show | 7 | HG00741.hp1 HG01069.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6169+424_6169+435d others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028924
|
GAAAAAAA others(6): Show |
G | 37 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(34): Show | 37 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.6169+423_6169+435d others(15): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028924
|
GAAAAAAA others(7): Show |
G | 38 | a0001c0002t0001g0277a0002c0093t0004g0122a0003c0069t0005g0219others(35): Show | 39 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.6169+422_6169+435d others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028924
|
GAAAAAAA others(8): Show |
G | 22 | a0004c0050t0014g0345a0005c0014t0001g0005a0005c0014t0001g0289others(19): Show | 23 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.6169+421_6169+435d others(17): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028924
|
GAAAAAAA others(9): Show |
G | 12 | a0002c0001t0006g0120a0005c0014t0001g0308a0005c0014t0001g0315others(9): Show | 12 | HG00642.hp2 HG00741.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.6169+420_6169+435d others(18): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028924
|
GAAAAAAA others(10): Show |
G | 4 | a0017c0022t0004g0130a0017c0022t0004g0131a0017c0022t0004g0252others(1): Show | 4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.6169+419_6169+435d others(19): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028924
|
GAAAAAAA others(13): Show |
G | 13 | a0004c0073t0002g0274a0004c0074t0002g0286a0005c0037t0004g0152others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.6169+416_6169+435d others(22): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028924
|
GAAAAAAA others(14): Show |
G | 42 | a0001c0002t0008g0136a0001c0002t0008g0137a0001c0002t0008g0139others(39): Show | 44 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.6169+415_6169+435d others(23): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028924
|
GAAAAAAA others(15): Show |
G | 2 | a0007c0006t0003g0052a0026c0036t0002g0203 | 2 | HG03225.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.6169+414_6169+435d others(24): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028924 | ||||||
| chr9:115028959
|
A | G | 3 | a0002c0001t0002g0100a0002c0020t0002g0148a0004c0004t0002g0301 | 3 | HG02300.hp1 NA18747.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.6169+401T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028959 | ||||||
| chr9:115028994
|
C | CT | 121 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(118): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.6169+365dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115028994 | ||||||
| chr9:115029035
|
G | GA | 100 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.6169+324dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029035 | ||||||
| chr9:115029035
|
G | GAA | 11 | a0001c0002t0008g0137a0001c0011t0001g0095a0002c0001t0002g0096others(8): Show | 11 | HG00597.hp2 HG00741.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.6169+323_6169+324d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029035 | ||||||
| chr9:115029035
|
GA | G | 46 | a0001c0009t0002g0117a0002c0001t0001g0165a0002c0001t0002g0082others(43): Show | 47 | HG00741.hp2 HG01081.hp2 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.6169+324delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029035 | ||||||
| chr9:115029038
|
A | G | 1 | a0053c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6169+322T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029038 | ||||||
| chr9:115029039
|
A | C | 4 | a0003c0069t0005g0219a0006c0007t0005g0357a0028c0038t0005g0353others(1): Show | 4 | HG02572.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.6169+321T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029039 | ||||||
| chr9:115029116
|
C | T | 1 | a0010c0008t0007g0021 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.6169+244G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029116 | ||||||
| chr9:115029117
|
G | A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6169+243C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029117 | ||||||
| chr9:115029127
|
T | A | 4 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(1): Show | 4 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.6169+233A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029127 | ||||||
| chr9:115029145
|
G | A | 1 | a0025c0039t0003g0042 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.6169+215C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029145 | ||||||
| chr9:115029233
|
G | C | 2 | a0001c0002t0001g0275a0001c0002t0001g0277 | 2 | HG01255.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.6169+127C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029233 | ||||||
| chr9:115029338
|
T | C | 57 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(54): Show | 57 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.6169+22A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 25/27 | chr9 | 115029338 | ||||||
| chr9:115029469
|
C | T | 1 | a0002c0001t0002g0158 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.6073-13G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115029469 | ||||||
| chr9:115029553
|
C | T | 1 | a0009c0092t0002g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6073-97G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115029553 | ||||||
| chr9:115029603
|
C | T | 1 | a0001c0002t0001g0277 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.6073-147G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115029603 | ||||||
| chr9:115029881
|
C | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6072+373G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115029881 | ||||||
| chr9:115029981
|
AT | A | 13 | a0001c0009t0002g0117a0005c0017t0001g0081a0005c0017t0002g0076others(10): Show | 14 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.6072+272delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115029981 | ||||||
| chr9:115029995
|
G | C | 56 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.6072+259C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115029995 | ||||||
| chr9:115030064
|
G | A | 3 | a0002c0001t0002g0098a0004c0004t0002g0297a0004c0004t0002g0307 | 3 | HG01978.hp1 HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.6072+190C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115030064 | ||||||
| chr9:115030117
|
C | T | 1 | a0004c0073t0002g0274 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6072+137G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115030117 | ||||||
| chr9:115030147
|
G | T | 118 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.6072+107C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115030147 | ||||||
| chr9:115030164
|
C | T | 5 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(2): Show | 5 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.6072+90G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115030164 | ||||||
| chr9:115030195
|
C | G | 1 | a0004c0018t0004g0334 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6072+59G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 24/27 | chr9 | 115030195 | ||||||
| chr9:115030477
|
C | G | 1 | a0003c0003t0019g0360 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5921-72G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030477 | ||||||
| chr9:115030597
|
A | T | 28 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(25): Show | 29 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.5921-192T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030597 | ||||||
| chr9:115030683
|
A | C | 1 | a0002c0001t0007g0018 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5921-278T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030683 | ||||||
| chr9:115030826
|
G | T | 2 | a0001c0024t0003g0008a0001c0024t0003g0009 | 2 | NA18992.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.5921-421C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030826 | ||||||
| chr9:115030831
|
C | T | 1 | a0009c0092t0002g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5921-426G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030831 | ||||||
| chr9:115030916
|
G | A | 1 | a0001c0002t0010g0288 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5921-511C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030916 | ||||||
| chr9:115030946
|
C | T | 1 | a0009c0019t0002g0173 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5921-541G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115030946 | ||||||
| chr9:115031079
|
T | G | 9 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(6): Show | 9 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5920+474A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031079 | ||||||
| chr9:115031134
|
G | T | 25 | a0008c0005t0001g0083a0008c0005t0001g0084a0008c0005t0001g0085others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.5920+419C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031134 | ||||||
| chr9:115031152
|
C | A | 2 | a0001c0002t0001g0306a0001c0002t0010g0330 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.5920+401G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031152 | ||||||
| chr9:115031179
|
G | T | 1 | a0001c0002t0008g0137 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.5920+374C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031179 | ||||||
| chr9:115031269
|
T | C | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5920+284A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031269 | ||||||
| chr9:115031356
|
G | A | 1 | a0004c0004t0002g0297 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.5920+197C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031356 | ||||||
| chr9:115031378
|
C | T | 32 | a0003c0069t0005g0219a0006c0007t0005g0200a0006c0007t0005g0204others(29): Show | 33 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.5920+175G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031378 | ||||||
| chr9:115031383
|
T | G | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5920+170A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031383 | ||||||
| chr9:115031387
|
C | T | 1 | a0003c0003t0019g0360 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5920+166G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031387 | ||||||
| chr9:115031453
|
G | A | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5920+100C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031453 | ||||||
| chr9:115031514
|
T | G | 2 | a0001c0009t0001g0188a0003c0003t0010g0328 | 2 | HG01515.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.5920+39A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 23/27 | chr9 | 115031514 | ||||||
| chr9:115031875
|
G | A | 56 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.5788-190C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115031875 | ||||||
| chr9:115032121
|
G | T | 1 | a0002c0001t0002g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5788-436C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115032121 | ||||||
| chr9:115032122
|
G | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5788-437C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115032122 | ||||||
| chr9:115032321
|
C | T | 1 | a0008c0005t0001g0118 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.5788-636G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115032321 | ||||||
| chr9:115032403
|
G | A | 3 | a0004c0051t0004g0342a0034c0060t0014g0253a0049c0064t0014g0343 | 3 | HG02257.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5788-718C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115032403 | ||||||
| chr9:115032614
|
TG | T | 11 | a0001c0002t0008g0136a0001c0002t0008g0137a0001c0002t0008g0139others(8): Show | 11 | HG01361.hp1 HG02015.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.5788-930delC | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115032614 | ||||||
| chr9:115033009
|
C | A | 56 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.5788-1324G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115033009 | ||||||
| chr9:115033153
|
C | G | 1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5788-1468G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115033153 | ||||||
| chr9:115033285
|
C | T | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5788-1600G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115033285 | ||||||
| chr9:115033320
|
C | G | 2 | a0029c0046t0004g0339a0029c0046t0004g0340 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5788-1635G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115033320 | ||||||
| chr9:115033864
|
T | G | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5787+1340A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115033864 | ||||||
| chr9:115034062
|
C | T | 17 | a0002c0001t0006g0120a0012c0012t0006g0057a0012c0012t0006g0058others(14): Show | 17 | HG00642.hp2 HG00741.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.5787+1142G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034062 | ||||||
| chr9:115034106
|
A | T | 2 | a0004c0018t0004g0292a0007c0086t0020g0044 | 2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.5787+1098T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034106 | ||||||
| chr9:115034118
|
G | A | 1 | a0001c0009t0001g0160 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.5787+1086C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034118 | ||||||
| chr9:115034132
|
A | G | 4 | a0002c0001t0006g0120a0012c0012t0006g0060a0014c0016t0006g0071others(1): Show | 4 | HG01169.hp2 HG01346.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.5787+1072T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034132 | ||||||
| chr9:115034136
|
G | A | 1 | a0053c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5787+1068C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034136 | ||||||
| chr9:115034187
|
G | A | 1 | a0053c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5787+1017C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034187 | ||||||
| chr9:115034218
|
A | G | 1 | a0002c0001t0002g0002 | 2 | NA19066.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.5787+986T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034218 | ||||||
| chr9:115034530
|
G | A | 4 | a0002c0001t0002g0168a0002c0020t0011g0132a0004c0004t0002g0220others(1): Show | 4 | NA18954.hp2 NA18961.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.5787+674C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034530 | ||||||
| chr9:115034683
|
G | A | 1 | a0006c0007t0027g0295 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.5787+521C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034683 | ||||||
| chr9:115034706
|
T | C | 1 | a0001c0009t0001g0160 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.5787+498A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034706 | ||||||
| chr9:115034707
|
T | C | 242 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(239): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.5787+497A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034707 | ||||||
| chr9:115034758
|
G | C | 3 | a0002c0001t0002g0100a0002c0020t0002g0148a0007c0006t0003g0028 | 3 | HG00558.hp1 NA18747.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.5787+446C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034758 | ||||||
| chr9:115034966
|
C | A | 1 | a0002c0001t0002g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5787+238G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115034966 | ||||||
| chr9:115035075
|
T | C | 1 | a0008c0005t0002g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.5787+129A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115035075 | ||||||
| chr9:115035080
|
A | AT | 272 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(269): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.5787+123dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115035080 | ||||||
| chr9:115035115
|
G | A | 27 | a0001c0009t0002g0117a0003c0027t0002g0214a0003c0027t0002g0215others(24): Show | 28 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.5787+89C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115035115 | ||||||
| chr9:115035128
|
A | G | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5787+76T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 22/27 | chr9 | 115035128 | ||||||
| chr9:115035439
|
G | T | 4 | a0002c0001t0006g0120a0012c0012t0006g0060a0014c0016t0006g0071others(1): Show | 4 | HG01169.hp2 HG01346.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.5657-105C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/27 | chr9 | 115035439 | ||||||
| chr9:115035610
|
C | T | 1 | a0044c0065t0005g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5657-276G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/27 | chr9 | 115035610 | ||||||
| chr9:115035882
|
C | T | 1 | a0003c0013t0008g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.5656+216G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/27 | chr9 | 115035882 | ||||||
| chr9:115035883
|
G | A | 23 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(20): Show | 24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.5656+215C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/27 | chr9 | 115035883 | ||||||
| chr9:115035968
|
G | A | 1 | a0001c0009t0001g0123 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5656+130C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/27 | chr9 | 115035968 | ||||||
| chr9:115035994
|
C | T | 1 | a0002c0001t0002g0100 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.5656+104G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 21/27 | chr9 | 115035994 | ||||||
| chr9:115036284
|
T | C | 1 | a0002c0001t0002g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5513-43A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036284 | ||||||
| chr9:115036336
|
G | A | 1 | a0002c0001t0002g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5513-95C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036336 | ||||||
| chr9:115036346
|
G | A | 3 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321 | 3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5513-105C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036346 | ||||||
| chr9:115036532
|
T | A | 3 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321 | 3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5513-291A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036532 | ||||||
| chr9:115036553
|
G | C | 35 | a0001c0009t0002g0117a0003c0027t0002g0214a0003c0027t0002g0215others(32): Show | 36 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.5513-312C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036553 | ||||||
| chr9:115036558
|
C | T | 56 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.5513-317G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036558 | ||||||
| chr9:115036559
|
G | A | 1 | a0002c0001t0001g0165 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.5513-318C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036559 | ||||||
| chr9:115036733
|
T | C | 1 | a0002c0001t0002g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.5513-492A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036733 | ||||||
| chr9:115036833
|
T | C | 1 | a0056c0078t0001g0294 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5513-592A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036833 | ||||||
| chr9:115036853
|
C | T | 1 | a0018c0028t0012g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5513-612G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115036853 | ||||||
| chr9:115037056
|
C | T | 23 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(20): Show | 24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.5513-815G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037056 | ||||||
| chr9:115037202
|
A | G | 1 | a0018c0028t0012g0258 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5513-961T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037202 | ||||||
| chr9:115037422
|
T | G | 3 | a0007c0006t0007g0001a0007c0006t0007g0051a0007c0006t0016g0050 | 4 | NA19000.hp1 NA19004.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.5512+839A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037422 | ||||||
| chr9:115037475
|
G | A | 9 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(6): Show | 9 | HG00323.hp1 HG00408.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.5512+786C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037475 | ||||||
| chr9:115037521
|
A | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5512+740T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037521 | ||||||
| chr9:115037525
|
A | T | 1 | a0002c0001t0002g0182 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.5512+736T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037525 | ||||||
| chr9:115037589
|
G | C | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5512+672C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037589 | ||||||
| chr9:115037778
|
C | T | 274 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(271): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.5512+483G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037778 | ||||||
| chr9:115037788
|
A | G | 37 | a0001c0009t0002g0117a0003c0027t0002g0214a0003c0027t0002g0215others(34): Show | 38 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.5512+473T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037788 | ||||||
| chr9:115037826
|
T | C | 251 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(248): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.5512+435A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037826 | ||||||
| chr9:115037855
|
G | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5512+406C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037855 | ||||||
| chr9:115037933
|
A | G | 1 | a0017c0022t0004g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5512+328T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115037933 | ||||||
| chr9:115038138
|
T | A | 41 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(38): Show | 41 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.5512+123A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115038138 | ||||||
| chr9:115038193
|
C | T | 2 | a0003c0003t0001g0329a0056c0078t0001g0294 | 2 | HG02486.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.5512+68G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 20/27 | chr9 | 115038193 | ||||||
| chr9:115038415
|
T | C | 6 | a0002c0020t0001g0145a0004c0004t0001g0269a0007c0006t0007g0006others(3): Show | 6 | NA18944.hp2 NA18948.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.5393-35A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115038415 | ||||||
| chr9:115038667
|
G | C | 1 | a0001c0002t0008g0136 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.5393-287C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115038667 | ||||||
| chr9:115038792
|
C | CCTTTTCT others(10): Show |
3 | a0001c0002t0001g0134a0001c0002t0013g0135a0001c0011t0001g0095 | 3 | HG02071.hp1 NA19067.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.5393-429_5393-413d others(19): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115038792 | ||||||
| chr9:115038897
|
G | A | 56 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.5393-517C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115038897 | ||||||
| chr9:115038909
|
C | G | 3 | a0003c0003t0004g0337a0024c0082t0004g0055a0027c0070t0002g0351 | 3 | HG02280.hp2 HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.5393-529G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115038909 | ||||||
| chr9:115038998
|
T | C | 3 | a0021c0032t0001g0317a0021c0032t0001g0319a0021c0032t0001g0320 | 3 | HG01123.hp2 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.5393-618A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115038998 | ||||||
| chr9:115039015
|
A | G | 1 | a0026c0036t0002g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5393-635T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039015 | ||||||
| chr9:115039131
|
C | G | 3 | a0004c0051t0004g0342a0034c0060t0014g0253a0049c0064t0014g0343 | 3 | HG02257.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5393-751G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039131 | ||||||
| chr9:115039191
|
C | T | 23 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(20): Show | 24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.5393-811G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039191 | ||||||
| chr9:115039215
|
C | T | 4 | a0025c0039t0003g0041a0025c0039t0003g0042a0035c0085t0003g0046others(1): Show | 4 | NA18950.hp2 NA18952.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.5393-835G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039215 | ||||||
| chr9:115039337
|
A | G | 1 | a0040c0091t0002g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.5393-957T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039337 | ||||||
| chr9:115039679
|
C | G | 1 | a0052c0057t0014g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5392+1262G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039679 | ||||||
| chr9:115039715
|
G | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5392+1226C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039715 | ||||||
| chr9:115039759
|
A | G | 1 | a0027c0071t0001g0355 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5392+1182T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039759 | ||||||
| chr9:115039817
|
A | G | 9 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(6): Show | 9 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5392+1124T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039817 | ||||||
| chr9:115039968
|
T | A | 17 | a0002c0001t0006g0120a0012c0012t0006g0057a0012c0012t0006g0058others(14): Show | 17 | HG00642.hp2 HG00741.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.5392+973A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115039968 | ||||||
| chr9:115040102
|
C | A | 1 | a0002c0001t0002g0195 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.5392+839G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040102 | ||||||
| chr9:115040196
|
T | A | 3 | a0001c0009t0001g0178a0003c0003t0019g0273a0003c0003t0019g0360 | 3 | HG01081.hp1 HG01261.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.5392+745A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040196 | ||||||
| chr9:115040211
|
T | G | 2 | a0005c0023t0001g0299a0005c0023t0001g0300 | 2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.5392+730A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040211 | ||||||
| chr9:115040281
|
C | T | 1 | a0005c0017t0002g0076 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5392+660G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040281 | ||||||
| chr9:115040344
|
C | T | 3 | a0006c0007t0005g0357a0028c0038t0005g0353a0028c0038t0005g0354 | 3 | HG02572.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.5392+597G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040344 | ||||||
| chr9:115040346
|
G | A | 2 | a0029c0046t0004g0339a0029c0046t0004g0340 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5392+595C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040346 | ||||||
| chr9:115040418
|
T | C | 9 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(6): Show | 9 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5392+523A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040418 | ||||||
| chr9:115040515
|
A | G | 1 | a0025c0039t0003g0041 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.5392+426T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040515 | ||||||
| chr9:115040706
|
G | T | 22 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(19): Show | 22 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.5392+235C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040706 | ||||||
| chr9:115040775
|
C | G | 1 | a0001c0009t0001g0178 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5392+166G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040775 | ||||||
| chr9:115040906
|
A | AACAC | 222 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.5392+31_5392+34dup others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040906 | ||||||
| chr9:115040906
|
A | AACACAC | 4 | a0004c0050t0014g0345a0005c0062t0026g0250a0009c0100t0005g0318others(1): Show | 4 | HG01192.hp1 HG02257.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.5392+29_5392+34dup others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 19/27 | chr9 | 115040906 | ||||||
| chr9:115041101
|
G | C | 10 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(7): Show | 10 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.5249-17C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041101 | ||||||
| chr9:115041232
|
C | T | 1 | a0006c0007t0005g0303 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5249-148G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041232 | ||||||
| chr9:115041250
|
G | T | 1 | a0005c0067t0002g0359 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5249-166C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041250 | ||||||
| chr9:115041300
|
C | CG | 3 | a0003c0052t0001g0234a0006c0007t0005g0221a0009c0100t0005g0318 | 3 | HG02818.hp1 NA18963.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.5249-217_5249-216i others(3): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041300 | ||||||
| chr9:115041300
|
CA | C | 47 | a0001c0009t0001g0155a0001c0009t0001g0160a0001c0009t0002g0117others(44): Show | 47 | HG01081.hp1 HG01109.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.5249-217delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041300 | ||||||
| chr9:115041300
|
CAG | C | 34 | a0001c0009t0001g0123a0001c0009t0015g0124a0001c0024t0003g0008others(31): Show | 35 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.5249-218_5249-217d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041300 | ||||||
| chr9:115041300
|
CAGG | C | 12 | a0001c0009t0015g0350a0001c0024t0015g0321a0003c0003t0004g0337others(9): Show | 12 | HG01361.hp2 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.5249-219_5249-217d others(5): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041300 | ||||||
| chr9:115041301
|
A | G | 37 | a0001c0002t0001g0298a0001c0002t0001g0305a0001c0009t0001g0101others(34): Show | 37 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.5249-217T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041301 | ||||||
| chr9:115041303
|
G | C | 1 | a0004c0018t0004g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5249-219C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041303 | ||||||
| chr9:115041304
|
A | AGCGGG | 13 | a0001c0002t0001g0138a0001c0002t0001g0141a0001c0002t0001g0142others(10): Show | 13 | HG03688.hp1 NA18942.hp1 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.5249-221_5249-220i others(7): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041304 | ||||||
| chr9:115041304
|
A | AGCGGGG | 21 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(18): Show | 21 | HG00597.hp1 HG00621.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.5249-221_5249-220i others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041304 | ||||||
| chr9:115041304
|
A | AGCGGGGG | 14 | a0001c0002t0001g0134a0001c0002t0001g0192a0001c0002t0001g0276others(11): Show | 14 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.5249-221_5249-220i others(9): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041304 | ||||||
| chr9:115041304
|
A | C | 14 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0226others(11): Show | 14 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(11): Show |
intron_variant | MODIFIER | c.5249-220T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041304 | ||||||
| chr9:115041304
|
A | G | 116 | a0001c0002t0001g0298a0001c0002t0001g0305a0001c0009t0001g0101others(113): Show | 117 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(114): Show |
intron_variant | MODIFIER | c.5249-220T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041304 | ||||||
| chr9:115041305
|
G | C | 10 | a0001c0002t0001g0298a0001c0002t0001g0305a0012c0012t0006g0060others(7): Show | 10 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.5249-221C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041305 | ||||||
| chr9:115041307
|
G | GC | 35 | a0008c0005t0001g0083a0008c0005t0001g0084a0008c0005t0001g0085others(32): Show | 35 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.5249-224_5249-223i others(3): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041307 | ||||||
| chr9:115041307
|
G | T | 2 | a0029c0046t0004g0339a0029c0046t0004g0340 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5249-223C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041307 | ||||||
| chr9:115041308
|
GC | G | 3 | a0004c0051t0004g0342a0034c0060t0014g0253a0049c0064t0014g0343 | 3 | HG02257.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5249-225delG | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041308 | ||||||
| chr9:115041309
|
C | G | 268 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(265): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.5249-225G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041309 | ||||||
| chr9:115041309
|
C | T | 1 | a0052c0057t0014g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5249-225G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041309 | ||||||
| chr9:115041311
|
G | C | 23 | a0003c0003t0001g0344a0005c0017t0001g0081a0005c0017t0002g0076others(20): Show | 24 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.5249-227C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041311 | ||||||
| chr9:115041312
|
G | C | 6 | a0001c0011t0008g0153a0005c0034t0002g0197a0005c0034t0002g0198others(3): Show | 6 | HG01109.hp2 HG01243.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.5249-228C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041312 | ||||||
| chr9:115041313
|
GGAA | G | 17 | a0001c0002t0001g0298a0001c0002t0001g0305a0012c0012t0006g0057others(14): Show | 17 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.5249-232_5249-230d others(5): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041313 | ||||||
| chr9:115041314
|
G | A | 54 | a0004c0050t0014g0345a0005c0014t0001g0005a0005c0014t0001g0289others(51): Show | 56 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.5249-230C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041314 | ||||||
| chr9:115041315
|
A | G | 182 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.5249-231T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041315 | ||||||
| chr9:115041316
|
A | G | 5 | a0003c0013t0001g0291a0012c0012t0006g0059a0021c0032t0001g0317others(2): Show | 5 | HG01099.hp1 HG01123.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.5249-232T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041316 | ||||||
| chr9:115041332
|
C | T | 1 | a0002c0093t0004g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5249-248G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041332 | ||||||
| chr9:115041441
|
G | A | 183 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.5249-357C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041441 | ||||||
| chr9:115041553
|
A | G | 54 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(51): Show | 55 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.5249-469T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041553 | ||||||
| chr9:115041603
|
A | G | 273 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.5249-519T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041603 | ||||||
| chr9:115041748
|
C | T | 52 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.5248+471G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115041748 | ||||||
| chr9:115042051
|
C | T | 1 | a0044c0065t0005g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5248+168G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115042051 | ||||||
| chr9:115042121
|
A | C | 10 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(7): Show | 10 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.5248+98T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 18/27 | chr9 | 115042121 | ||||||
| chr9:115042377
|
A | T | 1 | a0001c0024t0015g0321 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5126-36T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042377 | ||||||
| chr9:115042388
|
T | C | 17 | a0008c0005t0001g0083a0008c0005t0001g0084a0008c0005t0001g0085others(14): Show | 17 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(14): Show |
intron_variant | MODIFIER | c.5126-47A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042388 | ||||||
| chr9:115042589
|
C | T | 3 | a0005c0017t0001g0081a0005c0017t0002g0076a0045c0049t0002g0242 | 3 | HG01346.hp2 HG03704.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.5126-248G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042589 | ||||||
| chr9:115042652
|
C | G | 1 | a0009c0092t0002g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5126-311G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042652 | ||||||
| chr9:115042670
|
T | G | 6 | a0005c0037t0004g0152a0005c0037t0004g0271a0013c0021t0004g0129others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5126-329A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042670 | ||||||
| chr9:115042795
|
G | A | 4 | a0017c0022t0004g0130a0017c0022t0004g0131a0017c0022t0004g0252others(1): Show | 4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.5126-454C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042795 | ||||||
| chr9:115042889
|
C | T | 1 | a0053c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5126-548G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042889 | ||||||
| chr9:115042922
|
C | G | 37 | a0008c0005t0001g0083a0008c0005t0001g0084a0008c0005t0001g0085others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.5126-581G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115042922 | ||||||
| chr9:115043015
|
G | A | 273 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.5126-674C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043015 | ||||||
| chr9:115043067
|
A | G | 1 | a0005c0014t0001g0289 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.5126-726T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043067 | ||||||
| chr9:115043150
|
A | G | 2 | a0004c0050t0014g0345a0005c0062t0026g0250 | 2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5126-809T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043150 | ||||||
| chr9:115043280
|
T | C | 50 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.5126-939A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043280 | ||||||
| chr9:115043396
|
A | T | 1 | a0001c0002t0001g0323 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5126-1055T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043396 | ||||||
| chr9:115043440
|
C | A | 218 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.5126-1099G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043440 | ||||||
| chr9:115043485
|
C | T | 52 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.5126-1144G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043485 | ||||||
| chr9:115043547
|
A | G | 2 | a0004c0050t0014g0345a0005c0062t0026g0250 | 2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5126-1206T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043547 | ||||||
| chr9:115043639
|
T | A | 1 | a0026c0036t0002g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5126-1298A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043639 | ||||||
| chr9:115043736
|
A | AAAAC | 222 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.5126-1399_5126-139 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043736 | ||||||
| chr9:115043740
|
C | A | 6 | a0009c0031t0001g0166a0010c0008t0003g0013a0010c0008t0003g0014others(3): Show | 6 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.5126-1399G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043740 | ||||||
| chr9:115043798
|
C | T | 1 | a0009c0042t0008g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5126-1457G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043798 | ||||||
| chr9:115043966
|
C | T | 1 | a0018c0028t0012g0258 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5126-1625G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115043966 | ||||||
| chr9:115044088
|
A | G | 2 | a0034c0060t0014g0253a0049c0064t0014g0343 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.5126-1747T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044088 | ||||||
| chr9:115044200
|
A | G | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5126-1859T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044200 | ||||||
| chr9:115044262
|
T | TA | 55 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.5126-1922dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044262 | ||||||
| chr9:115044262
|
TA | T | 86 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.5126-1922delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044262 | ||||||
| chr9:115044274
|
AC | A | 4 | a0018c0028t0012g0258a0018c0028t0012g0259a0018c0028t0012g0260others(1): Show | 4 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.5126-1934delG | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044274 | ||||||
| chr9:115044384
|
G | GAC | 89 | a0001c0002t0008g0139a0001c0011t0001g0114a0002c0001t0001g0104others(86): Show | 90 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.5125+2024_5125+202 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | ||||||
| chr9:115044384
|
G | GACAC | 13 | a0002c0001t0002g0182a0002c0001t0007g0018a0003c0013t0008g0246others(10): Show | 14 | HG01993.hp1 HG02572.hp2 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.5125+2022_5125+202 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | ||||||
| chr9:115044384
|
G | GACACACA others(1): Show |
20 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(17): Show | 21 | HG00423.hp2 HG00609.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.5125+2018_5125+202 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | ||||||
| chr9:115044384
|
G | GACACACA others(3): Show |
1 | a0010c0008t0003g0026 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.5125+2016_5125+202 others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | ||||||
| chr9:115044384
|
GAC | G | 35 | a0004c0051t0004g0342a0006c0007t0005g0200a0006c0007t0005g0204others(32): Show | 36 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.5125+2024_5125+202 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | ||||||
| chr9:115044384
|
GACAC | G | 54 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0001g0133others(51): Show | 54 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(51): Show |
intron_variant | MODIFIER | c.5125+2022_5125+202 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | ||||||
| chr9:115044384
|
GACACAC | G | 83 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(80): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.5125+2020_5125+202 others(10): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044384 | ||||||
| chr9:115044429
|
G | A | 2 | a0002c0001t0002g0094a0002c0001t0002g0159 | 2 | HG02109.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.5125+1981C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044429 | ||||||
| chr9:115044503
|
G | A | 4 | a0005c0034t0002g0197a0005c0034t0002g0198a0005c0067t0002g0359others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.5125+1907C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044503 | ||||||
| chr9:115044527
|
T | G | 1 | a0018c0028t0012g0258 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5125+1883A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044527 | ||||||
| chr9:115044608
|
A | C | 2 | a0002c0001t0002g0092a0002c0001t0002g0112 | 2 | HG01169.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.5125+1802T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044608 | ||||||
| chr9:115044707
|
G | A | 5 | a0005c0103t0012g0091a0018c0028t0012g0258a0018c0028t0012g0259others(2): Show | 5 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.5125+1703C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044707 | ||||||
| chr9:115044781
|
C | T | 1 | a0002c0001t0002g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5125+1629G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044781 | ||||||
| chr9:115044785
|
G | A | 2 | a0004c0050t0014g0345a0005c0062t0026g0250 | 2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5125+1625C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115044785 | ||||||
| chr9:115045229
|
C | T | 23 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(20): Show | 23 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.5125+1181G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045229 | ||||||
| chr9:115045325
|
T | C | 1 | a0055c0079t0023g0194 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5125+1085A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045325 | ||||||
| chr9:115045429
|
C | T | 27 | a0006c0007t0005g0200a0006c0007t0005g0204a0006c0007t0005g0221others(24): Show | 28 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.5125+981G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045429 | ||||||
| chr9:115045541
|
A | AT | 72 | a0001c0002t0001g0268a0001c0009t0001g0101a0001c0009t0015g0124others(69): Show | 73 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.5125+868dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045541 | ||||||
| chr9:115045541
|
A | ATT | 24 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(21): Show | 25 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.5125+867_5125+868d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045541 | ||||||
| chr9:115045541
|
AT | A | 11 | a0001c0002t0001g0277a0001c0002t0010g0330a0001c0009t0001g0123others(8): Show | 11 | HG01070.hp2 HG01255.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.5125+868delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045541 | ||||||
| chr9:115045564
|
C | T | 360 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(357): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.5125+846G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045564 | ||||||
| chr9:115045801
|
G | A | 22 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(19): Show | 22 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.5125+609C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045801 | ||||||
| chr9:115045841
|
G | C | 77 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.5125+569C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045841 | ||||||
| chr9:115045848
|
C | T | 4 | a0002c0001t0002g0171a0002c0001t0002g0177a0002c0001t0002g0179others(1): Show | 4 | HG00733.hp2 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.5125+562G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115045848 | ||||||
| chr9:115046051
|
A | G | 3 | a0006c0007t0005g0357a0028c0038t0005g0353a0028c0038t0005g0354 | 3 | HG02572.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.5125+359T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115046051 | ||||||
| chr9:115046070
|
G | GT | 8 | a0004c0018t0004g0292a0004c0018t0004g0334a0004c0075t0004g0266others(5): Show | 8 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(5): Show |
intron_variant | MODIFIER | c.5125+339dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115046070 | ||||||
| chr9:115046071
|
TA | T | 21 | a0002c0020t0001g0145a0004c0004t0001g0269a0007c0006t0007g0006others(18): Show | 21 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.5125+338delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115046071 | ||||||
| chr9:115046168
|
G | A | 1 | a0016c0095t0025g0183 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5125+242C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115046168 | ||||||
| chr9:115046184
|
G | A | 25 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(22): Show | 26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.5125+226C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115046184 | ||||||
| chr9:115046209
|
C | T | 29 | a0006c0007t0005g0200a0006c0007t0005g0204a0006c0007t0005g0221others(26): Show | 30 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.5125+201G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 17/27 | chr9 | 115046209 | ||||||
| chr9:115047211
|
G | T | 1 | a0002c0001t0002g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4853-529C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047211 | ||||||
| chr9:115047240
|
C | CT | 87 | a0001c0002t0001g0128a0001c0002t0001g0141a0001c0002t0001g0142others(84): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.4853-559dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047240 | ||||||
| chr9:115047240
|
C | CTT | 88 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0192others(85): Show | 89 | HG00597.hp1 HG00621.hp1 HG01081.hp1 others(86): Show |
intron_variant | MODIFIER | c.4853-560_4853-559d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047240 | ||||||
| chr9:115047240
|
C | CTTT | 7 | a0001c0009t0001g0178a0003c0003t0001g0207a0003c0003t0001g0208others(4): Show | 7 | HG01261.hp2 HG03471.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.4853-561_4853-559d others(5): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047240 | ||||||
| chr9:115047361
|
T | C | 1 | a0001c0002t0001g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4853-679A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047361 | ||||||
| chr9:115047362
|
G | T | 1 | a0051c0097t0002g0186 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4853-680C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047362 | ||||||
| chr9:115047403
|
T | C | 5 | a0009c0100t0005g0318a0017c0022t0004g0130a0017c0022t0004g0131others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.4853-721A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047403 | ||||||
| chr9:115047631
|
T | C | 1 | a0002c0001t0002g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4852+629A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047631 | ||||||
| chr9:115047692
|
G | A | 1 | a0007c0041t0007g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4852+568C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047692 | ||||||
| chr9:115047757
|
C | T | 56 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.4852+503G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047757 | ||||||
| chr9:115047838
|
T | A | 26 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(23): Show | 26 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(23): Show |
intron_variant | MODIFIER | c.4852+422A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047838 | ||||||
| chr9:115047879
|
A | G | 218 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.4852+381T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047879 | ||||||
| chr9:115047962
|
A | T | 12 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(9): Show | 13 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.4852+298T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047962 | ||||||
| chr9:115047971
|
G | T | 52 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4852+289C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115047971 | ||||||
| chr9:115048016
|
G | A | 12 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(9): Show | 12 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(9): Show |
intron_variant | MODIFIER | c.4852+244C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115048016 | ||||||
| chr9:115048208
|
A | T | 1 | a0002c0001t0002g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4852+52T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 16/27 | chr9 | 115048208 | ||||||
| chr9:115048612
|
A | G | 2 | a0009c0042t0008g0105a0009c0042t0008g0106 | 2 | HG02015.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.4580-80T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048612 | ||||||
| chr9:115048681
|
T | G | 3 | a0002c0001t0002g0098a0004c0004t0002g0297a0004c0004t0002g0307 | 3 | HG01978.hp1 HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.4580-149A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048681 | ||||||
| chr9:115048730
|
G | A | 3 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321 | 3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4580-198C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048730 | ||||||
| chr9:115048879
|
G | C | 4 | a0003c0003t0004g0337a0024c0082t0004g0055a0027c0070t0002g0351others(1): Show | 4 | HG02280.hp2 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4580-347C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048879 | ||||||
| chr9:115048906
|
G | A | 5 | a0004c0004t0001g0269a0005c0034t0002g0197a0005c0034t0002g0198others(2): Show | 5 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.4580-374C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048906 | ||||||
| chr9:115048926
|
T | C | 12 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(9): Show | 12 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(9): Show |
intron_variant | MODIFIER | c.4580-394A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048926 | ||||||
| chr9:115048987
|
C | T | 1 | a0006c0007t0027g0295 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4580-455G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115048987 | ||||||
| chr9:115049036
|
G | C | 273 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.4580-504C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049036 | ||||||
| chr9:115049072
|
G | GT | 222 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.4580-541dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049072 | ||||||
| chr9:115049429
|
C | T | 1 | a0002c0001t0002g0184 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4580-897G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049429 | ||||||
| chr9:115049499
|
C | T | 4 | a0017c0022t0004g0130a0017c0022t0004g0131a0017c0022t0004g0252others(1): Show | 4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.4580-967G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049499 | ||||||
| chr9:115049517
|
T | C | 224 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.4580-985A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049517 | ||||||
| chr9:115049592
|
G | C | 1 | a0003c0003t0001g0336 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4580-1060C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049592 | ||||||
| chr9:115049656
|
T | A | 4 | a0002c0001t0002g0157a0002c0001t0002g0170a0002c0001t0002g0190others(1): Show | 4 | HG02040.hp2 HG02155.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.4580-1124A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049656 | ||||||
| chr9:115049677
|
AT | A | 217 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.4580-1146delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049677 | ||||||
| chr9:115049743
|
C | T | 1 | a0047c0054t0005g0236 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4580-1211G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049743 | ||||||
| chr9:115049790
|
G | C | 1 | a0003c0003t0001g0216 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4580-1258C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049790 | ||||||
| chr9:115049833
|
A | T | 22 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(19): Show | 22 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.4580-1301T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049833 | ||||||
| chr9:115049888
|
T | C | 2 | a0004c0050t0014g0345a0005c0062t0026g0250 | 2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.4580-1356A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049888 | ||||||
| chr9:115049965
|
G | A | 1 | a0005c0023t0001g0300 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4580-1433C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115049965 | ||||||
| chr9:115050021
|
A | G | 2 | a0009c0042t0008g0105a0009c0042t0008g0106 | 2 | HG02015.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.4580-1489T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050021 | ||||||
| chr9:115050066
|
A | G | 218 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.4580-1534T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050066 | ||||||
| chr9:115050121
|
A | G | 242 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(239): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.4580-1589T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050121 | ||||||
| chr9:115050252
|
T | C | 27 | a0003c0035t0004g0150a0003c0035t0004g0151a0003c0077t0004g0356others(24): Show | 28 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.4580-1720A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050252 | ||||||
| chr9:115050278
|
A | G | 4 | a0018c0028t0012g0258a0018c0028t0012g0259a0018c0028t0012g0260others(1): Show | 4 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4580-1746T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050278 | ||||||
| chr9:115050347
|
G | A | 6 | a0005c0037t0004g0152a0005c0037t0004g0271a0013c0021t0004g0129others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.4580-1815C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050347 | ||||||
| chr9:115050462
|
C | T | 4 | a0017c0022t0004g0130a0017c0022t0004g0131a0017c0022t0004g0252others(1): Show | 4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.4580-1930G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050462 | ||||||
| chr9:115050498
|
T | C | 31 | a0006c0007t0005g0200a0006c0007t0005g0204a0006c0007t0005g0221others(28): Show | 32 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.4580-1966A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050498 | ||||||
| chr9:115050512
|
A | G | 12 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(9): Show | 12 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(9): Show |
intron_variant | MODIFIER | c.4580-1980T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050512 | ||||||
| chr9:115050612
|
C | A | 27 | a0003c0035t0004g0150a0003c0035t0004g0151a0003c0077t0004g0356others(24): Show | 28 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.4580-2080G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050612 | ||||||
| chr9:115050903
|
AC | A | 4 | a0011c0010t0001g0064a0011c0010t0001g0227a0011c0010t0001g0228others(1): Show | 4 | HG02258.hp1 HG02615.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.4580-2372delG | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115050903 | ||||||
| chr9:115051056
|
G | A | 214 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.4580-2524C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051056 | ||||||
| chr9:115051085
|
G | A | 52 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4580-2553C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051085 | ||||||
| chr9:115051148
|
G | A | 1 | a0009c0019t0002g0173 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4580-2616C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051148 | ||||||
| chr9:115051176
|
C | T | 214 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.4580-2644G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051176 | ||||||
| chr9:115051312
|
G | T | 214 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.4580-2780C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051312 | ||||||
| chr9:115051404
|
G | A | 1 | a0004c0004t0002g0325 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4580-2872C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051404 | ||||||
| chr9:115051511
|
G | T | 1 | a0002c0093t0004g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4580-2979C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051511 | ||||||
| chr9:115051537
|
CT | C | 215 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.4580-3006delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051537 | ||||||
| chr9:115051588
|
A | G | 214 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.4580-3056T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051588 | ||||||
| chr9:115051641
|
G | A | 25 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(22): Show | 26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4580-3109C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051641 | ||||||
| chr9:115051648
|
G | A | 1 | a0046c0053t0018g0245 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4580-3116C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051648 | ||||||
| chr9:115051695
|
T | G | 215 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.4580-3163A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051695 | ||||||
| chr9:115051711
|
C | T | 214 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.4580-3179G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051711 | ||||||
| chr9:115051822
|
G | T | 3 | a0023c0033t0001g0126a0023c0033t0001g0127a0023c0033t0001g0338 | 3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4580-3290C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051822 | ||||||
| chr9:115051874
|
T | C | 5 | a0005c0103t0012g0091a0018c0028t0012g0258a0018c0028t0012g0259others(2): Show | 5 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.4580-3342A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115051874 | ||||||
| chr9:115052023
|
T | TATAG | 242 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(239): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.4580-3495_4580-349 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052023 | ||||||
| chr9:115052079
|
C | CATATATA others(19): Show |
1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4580-3548_4580-354 others(30): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052079 | ||||||
| chr9:115052079
|
CAT | C | 53 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(50): Show | 55 | HG00621.hp2 HG01074.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.4580-3549_4580-354 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052079 | ||||||
| chr9:115052154
|
T | G | 1 | a0002c0001t0002g0190 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4580-3622A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052154 | ||||||
| chr9:115052475
|
C | CAATA | 44 | a0001c0002t0001g0267a0001c0002t0001g0327a0001c0009t0001g0244others(41): Show | 44 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.4580-3947_4580-394 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052475 | ||||||
| chr9:115052475
|
C | CAATAAAT others(1): Show |
29 | a0003c0003t0004g0337a0004c0018t0004g0292a0005c0023t0001g0299others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.4580-3951_4580-394 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052475 | ||||||
| chr9:115052475
|
CAATA | C | 5 | a0001c0002t0001g0128a0001c0002t0001g0192a0001c0002t0001g0322others(2): Show | 5 | HG00323.hp1 HG02970.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.4580-3947_4580-394 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052475 | ||||||
| chr9:115052475
|
CAATAAAT others(1): Show |
C | 57 | a0003c0035t0004g0150a0003c0035t0004g0151a0003c0077t0004g0356others(54): Show | 59 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.4580-3951_4580-394 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052475 | ||||||
| chr9:115052732
|
T | C | 25 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(22): Show | 26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4580-4200A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052732 | ||||||
| chr9:115052757
|
G | A | 24 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(21): Show | 25 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.4580-4225C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052757 | ||||||
| chr9:115052807
|
G | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4580-4275C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052807 | ||||||
| chr9:115052945
|
G | C | 1 | a0001c0002t0001g0298 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4579+4208C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052945 | ||||||
| chr9:115052994
|
G | A | 77 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.4579+4159C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115052994 | ||||||
| chr9:115053027
|
A | G | 3 | a0004c0051t0004g0342a0034c0060t0014g0253a0049c0064t0014g0343 | 3 | HG02257.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4579+4126T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053027 | ||||||
| chr9:115053143
|
G | A | 1 | a0004c0004t0002g0325 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4579+4010C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053143 | ||||||
| chr9:115053147
|
G | A | 2 | a0002c0001t0002g0103a0002c0001t0006g0120 | 2 | HG01169.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.4579+4006C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053147 | ||||||
| chr9:115053234
|
T | C | 52 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4579+3919A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053234 | ||||||
| chr9:115053268
|
C | T | 1 | a0022c0025t0001g0349 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4579+3885G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053268 | ||||||
| chr9:115053334
|
C | T | 273 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.4579+3819G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053334 | ||||||
| chr9:115053807
|
C | A | 214 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.4579+3346G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053807 | ||||||
| chr9:115053881
|
A | C | 27 | a0003c0035t0004g0150a0003c0035t0004g0151a0003c0077t0004g0356others(24): Show | 28 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.4579+3272T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053881 | ||||||
| chr9:115053937
|
T | C | 3 | a0012c0012t0006g0060a0014c0016t0006g0071a0014c0016t0006g0073 | 3 | HG01346.hp1 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4579+3216A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053937 | ||||||
| chr9:115053951
|
C | T | 2 | a0002c0001t0002g0169a0002c0001t0002g0185 | 2 | HG00642.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.4579+3202G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115053951 | ||||||
| chr9:115054003
|
T | C | 25 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(22): Show | 26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4579+3150A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054003 | ||||||
| chr9:115054009
|
T | C | 1 | a0018c0028t0012g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4579+3144A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054009 | ||||||
| chr9:115054091
|
G | A | 52 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4579+3062C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054091 | ||||||
| chr9:115054092
|
C | A | 52 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4579+3061G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054092 | ||||||
| chr9:115054148
|
C | T | 1 | a0005c0037t0004g0152 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4579+3005G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054148 | ||||||
| chr9:115054257
|
C | T | 1 | a0029c0046t0004g0339 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4579+2896G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054257 | ||||||
| chr9:115054328
|
G | A | 1 | a0026c0036t0002g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4579+2825C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054328 | ||||||
| chr9:115054385
|
T | C | 1 | a0004c0045t0002g0230 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4579+2768A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054385 | ||||||
| chr9:115054494
|
T | C | 1 | a0019c0026t0006g0068 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4579+2659A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054494 | ||||||
| chr9:115054595
|
C | T | 1 | a0023c0033t0001g0338 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4579+2558G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054595 | ||||||
| chr9:115054745
|
C | G | 1 | a0004c0074t0002g0286 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4579+2408G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054745 | ||||||
| chr9:115054776
|
A | C | 4 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(1): Show | 4 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.4579+2377T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054776 | ||||||
| chr9:115054882
|
T | G | 1 | a0001c0011t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4579+2271A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054882 | ||||||
| chr9:115054904
|
A | G | 1 | a0004c0075t0004g0266 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4579+2249T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054904 | ||||||
| chr9:115054995
|
T | G | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4579+2158A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115054995 | ||||||
| chr9:115055017
|
T | C | 4 | a0005c0034t0002g0197a0005c0034t0002g0198a0005c0067t0002g0359others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.4579+2136A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055017 | ||||||
| chr9:115055038
|
A | G | 24 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(21): Show | 25 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.4579+2115T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055038 | ||||||
| chr9:115055047
|
A | G | 269 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(266): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.4579+2106T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055047 | ||||||
| chr9:115055072
|
T | G | 52 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4579+2081A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055072 | ||||||
| chr9:115055075
|
C | T | 24 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(21): Show | 25 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.4579+2078G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055075 | ||||||
| chr9:115055126
|
T | G | 52 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4579+2027A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055126 | ||||||
| chr9:115055317
|
G | C | 14 | a0002c0001t0002g0092a0002c0001t0002g0098a0002c0001t0002g0110others(11): Show | 14 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.4579+1836C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055317 | ||||||
| chr9:115055404
|
G | A | 87 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.4579+1749C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055404 | ||||||
| chr9:115055428
|
A | C | 1 | a0002c0001t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4579+1725T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055428 | ||||||
| chr9:115055429
|
T | C | 1 | a0002c0001t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4579+1724A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055429 | ||||||
| chr9:115055497
|
G | A | 16 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(13): Show | 17 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4579+1656C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055497 | ||||||
| chr9:115055522
|
C | CA | 166 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.4579+1630dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055522 | ||||||
| chr9:115055843
|
T | G | 52 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4579+1310A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055843 | ||||||
| chr9:115055900
|
T | G | 220 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.4579+1253A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115055900 | ||||||
| chr9:115056203
|
A | AT | 56 | a0001c0002t0010g0288a0003c0027t0002g0214a0003c0027t0002g0215others(53): Show | 57 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.4579+949dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056203 | ||||||
| chr9:115056203
|
AT | A | 16 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(13): Show | 17 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4579+949delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056203 | ||||||
| chr9:115056264
|
C | A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4579+889G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056264 | ||||||
| chr9:115056289
|
C | T | 1 | a0015c0029t0003g0010 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4579+864G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056289 | ||||||
| chr9:115056539
|
C | A | 1 | a0002c0098t0002g0147 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4579+614G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056539 | ||||||
| chr9:115056557
|
C | T | 1 | a0019c0026t0006g0075 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.4579+596G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056557 | ||||||
| chr9:115056584
|
G | C | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4579+569C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056584 | ||||||
| chr9:115056696
|
C | T | 1 | a0002c0001t0002g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4579+457G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056696 | ||||||
| chr9:115056724
|
A | C | 28 | a0006c0007t0005g0200a0006c0007t0005g0204a0006c0007t0005g0221others(25): Show | 29 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.4579+429T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056724 | ||||||
| chr9:115056738
|
C | T | 3 | a0007c0006t0007g0001a0007c0006t0007g0051a0007c0006t0016g0050 | 4 | NA19000.hp1 NA19004.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.4579+415G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115056738 | ||||||
| chr9:115057005
|
A | T | 1 | a0018c0028t0012g0259 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4579+148T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115057005 | ||||||
| chr9:115057046
|
T | C | 1 | a0001c0002t0001g0141 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4579+107A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115057046 | ||||||
| chr9:115057079
|
G | A | 1 | a0007c0006t0007g0006 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4579+74C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115057079 | ||||||
| chr9:115057110
|
A | T | 50 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.4579+43T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115057110 | ||||||
| chr9:115057150
|
T | C | 1 | a0015c0040t0003g0040 | 1 | NA18961.hp1 | splice_region_variant&intron_variant | LOW | c.4579+3A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 15/27 | chr9 | 115057150 | ||||||
| chr9:115057469
|
GTTAA | G | 52 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.4307-48_4307-45del others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115057469 | ||||||
| chr9:115057762
|
G | T | 4 | a0017c0022t0004g0130a0017c0022t0004g0131a0017c0022t0004g0252others(1): Show | 4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.4307-337C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115057762 | ||||||
| chr9:115057926
|
C | A | 2 | a0001c0002t0001g0134a0001c0011t0001g0095 | 2 | HG02071.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.4307-501G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115057926 | ||||||
| chr9:115057946
|
C | T | 7 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.4307-521G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115057946 | ||||||
| chr9:115058241
|
G | A | 4 | a0013c0021t0004g0129a0013c0021t0004g0254a0013c0021t0004g0255others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.4307-816C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058241 | ||||||
| chr9:115058270
|
G | C | 27 | a0003c0035t0004g0150a0003c0035t0004g0151a0003c0077t0004g0356others(24): Show | 28 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.4307-845C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058270 | ||||||
| chr9:115058303
|
T | C | 1 | a0028c0038t0005g0354 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4307-878A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058303 | ||||||
| chr9:115058360
|
T | C | 1 | a0003c0069t0005g0219 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4307-935A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058360 | ||||||
| chr9:115058363
|
C | A | 16 | a0012c0012t0006g0057a0012c0012t0006g0058a0012c0012t0006g0059others(13): Show | 16 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.4307-938G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058363 | ||||||
| chr9:115058385
|
C | A | 1 | a0001c0094t0008g0176 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4307-960G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058385 | ||||||
| chr9:115058408
|
A | G | 2 | a0030c0047t0001g0358a0033c0058t0001g0248 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4307-983T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058408 | ||||||
| chr9:115058551
|
A | C | 2 | a0009c0100t0005g0318a0055c0079t0023g0194 | 2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4307-1126T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058551 | ||||||
| chr9:115058747
|
A | G | 163 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.4306+983T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058747 | ||||||
| chr9:115058810
|
T | A | 2 | a0030c0047t0001g0358a0033c0058t0001g0248 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4306+920A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058810 | ||||||
| chr9:115058864
|
C | T | 4 | a0002c0001t0002g0157a0002c0001t0002g0170a0002c0001t0002g0190others(1): Show | 4 | HG02040.hp2 HG02155.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.4306+866G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115058864 | ||||||
| chr9:115059123
|
CT | C | 77 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.4306+606delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115059123 | ||||||
| chr9:115059163
|
G | A | 4 | a0003c0003t0004g0337a0024c0082t0004g0055a0027c0070t0002g0351others(1): Show | 4 | HG02280.hp2 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4306+567C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115059163 | ||||||
| chr9:115059339
|
A | C | 163 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.4306+391T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115059339 | ||||||
| chr9:115059380
|
G | T | 1 | a0003c0003t0004g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4306+350C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115059380 | ||||||
| chr9:115059467
|
A | C | 40 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(37): Show | 40 | HG01081.hp1 HG01175.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.4306+263T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115059467 | ||||||
| chr9:115059611
|
G | A | 7 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(4): Show | 7 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.4306+119C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 14/27 | chr9 | 115059611 | ||||||
| chr9:115060073
|
C | T | 2 | a0001c0011t0001g0114a0046c0053t0018g0245 | 2 | HG00323.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.4034-71G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060073 | ||||||
| chr9:115060335
|
A | G | 23 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(20): Show | 23 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.4034-333T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060335 | ||||||
| chr9:115060522
|
A | T | 3 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321 | 3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4034-520T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060522 | ||||||
| chr9:115060731
|
T | C | 77 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.4034-729A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060731 | ||||||
| chr9:115060744
|
G | A | 6 | a0011c0010t0001g0064a0011c0010t0001g0227a0011c0010t0001g0228others(3): Show | 6 | HG02258.hp1 HG02615.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.4034-742C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060744 | ||||||
| chr9:115060835
|
C | T | 161 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.4034-833G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060835 | ||||||
| chr9:115060902
|
C | T | 16 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(13): Show | 17 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4034-900G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115060902 | ||||||
| chr9:115061496
|
A | G | 244 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.4033+1421T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115061496 | ||||||
| chr9:115061622
|
T | C | 84 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.4033+1295A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115061622 | ||||||
| chr9:115061794
|
T | C | 273 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.4033+1123A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115061794 | ||||||
| chr9:115061830
|
C | T | 2 | a0001c0011t0001g0114a0046c0053t0018g0245 | 2 | HG00323.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.4033+1087G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115061830 | ||||||
| chr9:115061939
|
T | C | 4 | a0003c0003t0004g0337a0024c0082t0004g0055a0027c0070t0002g0351others(1): Show | 4 | HG02280.hp2 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4033+978A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115061939 | ||||||
| chr9:115062029
|
G | T | 273 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.4033+888C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062029 | ||||||
| chr9:115062053
|
G | A | 162 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.4033+864C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062053 | ||||||
| chr9:115062086
|
T | C | 1 | a0039c0090t0001g0116 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.4033+831A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062086 | ||||||
| chr9:115062147
|
G | A | 1 | a0028c0038t0005g0354 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4033+770C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062147 | ||||||
| chr9:115062196
|
G | A | 25 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(22): Show | 26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4033+721C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062196 | ||||||
| chr9:115062367
|
G | A | 1 | a0055c0079t0023g0194 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4033+550C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062367 | ||||||
| chr9:115062428
|
G | A | 1 | a0008c0005t0001g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4033+489C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062428 | ||||||
| chr9:115062449
|
A | G | 1 | a0003c0052t0001g0234 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.4033+468T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062449 | ||||||
| chr9:115062479
|
C | T | 1 | a0014c0016t0006g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4033+438G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062479 | ||||||
| chr9:115062567
|
C | T | 25 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(22): Show | 26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4033+350G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062567 | ||||||
| chr9:115062608
|
CA | C | 143 | a0001c0002t0008g0136a0001c0009t0001g0123a0001c0009t0001g0188others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.4033+308delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062608 | ||||||
| chr9:115062652
|
T | C | 4 | a0005c0061t0002g0257a0023c0033t0001g0126a0023c0033t0001g0127others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.4033+265A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062652 | ||||||
| chr9:115062661
|
A | G | 25 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(22): Show | 26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4033+256T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062661 | ||||||
| chr9:115062701
|
T | G | 1 | a0004c0018t0004g0213 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4033+216A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062701 | ||||||
| chr9:115062742
|
T | A | 1 | a0004c0004t0002g0312 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4033+175A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062742 | ||||||
| chr9:115062761
|
G | A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4033+156C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062761 | ||||||
| chr9:115062806
|
G | A | 16 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(13): Show | 17 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4033+111C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 13/27 | chr9 | 115062806 | ||||||
| chr9:115063286
|
T | C | 1 | a0050c0063t0012g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3761-97A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063286 | ||||||
| chr9:115063310
|
C | T | 1 | a0001c0009t0001g0188 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3761-121G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063310 | ||||||
| chr9:115063312
|
T | A | 1 | a0003c0003t0001g0208 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3761-123A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063312 | ||||||
| chr9:115063325
|
G | A | 12 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(9): Show | 12 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(9): Show |
intron_variant | MODIFIER | c.3761-136C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063325 | ||||||
| chr9:115063646
|
G | T | 1 | a0055c0079t0023g0194 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3760+150C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063646 | ||||||
| chr9:115063667
|
C | T | 2 | a0005c0023t0001g0299a0005c0023t0001g0300 | 2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.3760+129G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063667 | ||||||
| chr9:115063723
|
C | T | 1 | a0053c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3760+73G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063723 | ||||||
| chr9:115063729
|
A | G | 2 | a0009c0100t0005g0318a0055c0079t0023g0194 | 2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3760+67T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 12/27 | chr9 | 115063729 | ||||||
| chr9:115064514
|
C | T | 1 | a0003c0003t0001g0239 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3487+133G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 11/27 | chr9 | 115064514 | ||||||
| chr9:115064515
|
G | T | 5 | a0014c0016t0006g0069a0014c0016t0006g0074a0019c0026t0006g0068others(2): Show | 5 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.3487+132C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 11/27 | chr9 | 115064515 | ||||||
| chr9:115064555
|
C | T | 4 | a0005c0034t0002g0197a0005c0034t0002g0198a0005c0067t0002g0359others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.3487+92G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 11/27 | chr9 | 115064555 | ||||||
| chr9:115065166
|
T | A | 2 | a0002c0001t0002g0169a0002c0001t0002g0185 | 2 | HG00642.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.3215-247A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065166 | ||||||
| chr9:115065310
|
C | T | 15 | a0008c0005t0001g0083a0008c0005t0001g0084a0008c0005t0001g0085others(12): Show | 15 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.3215-391G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065310 | ||||||
| chr9:115065373
|
G | A | 51 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(48): Show | 51 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.3215-454C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065373 | ||||||
| chr9:115065561
|
T | C | 1 | a0004c0004t0001g0269 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3215-642A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065561 | ||||||
| chr9:115065563
|
A | G | 11 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(8): Show | 12 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3215-644T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065563 | ||||||
| chr9:115065700
|
A | G | 1 | a0001c0009t0001g0244 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3215-781T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065700 | ||||||
| chr9:115065901
|
C | CA | 43 | a0001c0024t0015g0321a0001c0094t0008g0176a0002c0001t0001g0165others(40): Show | 43 | HG00423.hp1 HG00609.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.3215-983dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065901 | ||||||
| chr9:115065901
|
CA | C | 39 | a0001c0002t0001g0277a0001c0009t0001g0155a0001c0011t0001g0114others(36): Show | 40 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.3215-983delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115065901 | ||||||
| chr9:115066154
|
T | A | 1 | a0021c0032t0001g0320 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3215-1235A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066154 | ||||||
| chr9:115066195
|
C | T | 1 | a0002c0020t0002g0148 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3215-1276G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066195 | ||||||
| chr9:115066214
|
G | A | 1 | a0027c0070t0002g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3215-1295C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066214 | ||||||
| chr9:115066309
|
C | A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3215-1390G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066309 | ||||||
| chr9:115066338
|
G | A | 1 | a0004c0004t0002g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3215-1419C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066338 | ||||||
| chr9:115066394
|
T | A | 22 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(19): Show | 22 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.3215-1475A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066394 | ||||||
| chr9:115066560
|
T | A | 11 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(8): Show | 12 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3215-1641A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066560 | ||||||
| chr9:115066651
|
T | A | 10 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(7): Show | 10 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.3215-1732A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066651 | ||||||
| chr9:115066740
|
T | C | 1 | a0015c0029t0003g0010 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3215-1821A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066740 | ||||||
| chr9:115066778
|
A | G | 1 | a0001c0002t0001g0298 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3215-1859T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066778 | ||||||
| chr9:115066910
|
C | A | 1 | a0003c0003t0001g0208 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3215-1991G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115066910 | ||||||
| chr9:115067196
|
G | A | 3 | a0004c0004t0002g0301a0004c0045t0002g0230a0004c0045t0002g0231 | 3 | HG01358.hp2 HG01928.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.3215-2277C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115067196 | ||||||
| chr9:115067239
|
T | G | 1 | a0001c0009t0001g0123 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3215-2320A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115067239 | ||||||
| chr9:115067346
|
TTTTG | T | 57 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(54): Show | 58 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.3215-2431_3215-242 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115067346 | ||||||
| chr9:115067435
|
C | T | 6 | a0005c0037t0004g0152a0005c0037t0004g0271a0013c0021t0004g0129others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3215-2516G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115067435 | ||||||
| chr9:115067546
|
G | T | 1 | a0012c0012t0006g0063 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3215-2627C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115067546 | ||||||
| chr9:115067708
|
C | A | 141 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.3215-2789G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115067708 | ||||||
| chr9:115068509
|
C | A | 6 | a0005c0037t0004g0152a0005c0037t0004g0271a0013c0021t0004g0129others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3215-3590G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068509 | ||||||
| chr9:115068533
|
G | A | 57 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(54): Show | 58 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.3215-3614C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068533 | ||||||
| chr9:115068759
|
A | T | 1 | a0017c0022t0004g0130 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3215-3840T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068759 | ||||||
| chr9:115068793
|
T | A | 5 | a0005c0103t0012g0091a0018c0028t0012g0258a0018c0028t0012g0259others(2): Show | 5 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3215-3874A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068793 | ||||||
| chr9:115068843
|
C | T | 5 | a0009c0100t0005g0318a0017c0022t0004g0130a0017c0022t0004g0131others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3215-3924G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068843 | ||||||
| chr9:115068866
|
G | A | 360 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(357): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.3215-3947C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068866 | ||||||
| chr9:115068914
|
T | C | 30 | a0006c0007t0005g0200a0006c0007t0005g0204a0006c0007t0005g0221others(27): Show | 31 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.3215-3995A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068914 | ||||||
| chr9:115068987
|
C | T | 1 | a0019c0026t0006g0068 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3215-4068G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115068987 | ||||||
| chr9:115069041
|
T | C | 1 | a0002c0001t0002g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3215-4122A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069041 | ||||||
| chr9:115069042
|
A | G | 4 | a0005c0034t0002g0197a0005c0034t0002g0198a0005c0067t0002g0359others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.3215-4123T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069042 | ||||||
| chr9:115069161
|
T | A | 1 | a0001c0002t0001g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3215-4242A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069161 | ||||||
| chr9:115069225
|
G | A | 3 | a0003c0027t0002g0215a0026c0036t0002g0202a0026c0036t0002g0203 | 3 | HG02976.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3215-4306C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069225 | ||||||
| chr9:115069438
|
A | G | 56 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(53): Show | 57 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.3214+4165T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069438 | ||||||
| chr9:115069520
|
C | A | 23 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(20): Show | 23 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.3214+4083G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069520 | ||||||
| chr9:115069558
|
G | T | 4 | a0017c0022t0004g0130a0017c0022t0004g0131a0017c0022t0004g0252others(1): Show | 4 | HG02647.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3214+4045C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069558 | ||||||
| chr9:115069572
|
TTCCCTCC others(53): Show |
T | 1 | a0010c0008t0001g0077 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3214+3971_3214+403 others(64): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069572 | ||||||
| chr9:115069597
|
T | C | 1 | a0006c0007t0005g0200 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3214+4006A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069597 | ||||||
| chr9:115069602
|
C | T | 55 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(52): Show | 56 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.3214+4001G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069602 | ||||||
| chr9:115069602
|
CCCTCCCT others(33): Show |
C | 1 | a0030c0047t0001g0358 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3214+3961_3214+400 others(44): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069602 | ||||||
| chr9:115069606
|
CCCTCCCT others(121): Show |
C | 1 | a0018c0028t0012g0259 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3214+3869_3214+399 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069606 | ||||||
| chr9:115069607
|
CCTCCCTC others(5): Show |
C | 59 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(56): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.3214+3984_3214+399 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069607 | ||||||
| chr9:115069610
|
C | T | 7 | a0008c0005t0001g0083a0008c0005t0001g0115a0008c0005t0001g0121others(4): Show | 7 | HG00099.hp2 HG01070.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.3214+3993G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069610 | ||||||
| chr9:115069611
|
CCTCCCTC others(1): Show |
C | 14 | a0003c0003t0019g0360a0005c0037t0004g0152a0005c0037t0004g0271others(11): Show | 14 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.3214+3984_3214+399 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069611 | ||||||
| chr9:115069614
|
CCCTCTCT others(105): Show |
C | 2 | a0018c0028t0012g0258a0018c0028t0012g0260 | 2 | HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3214+3877_3214+398 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069614 | ||||||
| chr9:115069615
|
CCTCT | C | 36 | a0001c0009t0001g0155a0001c0009t0001g0160a0001c0009t0001g0188others(33): Show | 36 | HG00099.hp1 HG00323.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.3214+3984_3214+398 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069615 | ||||||
| chr9:115069618
|
CTCTCCCT others(109): Show |
C | 1 | a0050c0063t0012g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3214+3869_3214+398 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069618 | ||||||
| chr9:115069619
|
T | C | 118 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(115): Show | 120 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.3214+3984A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069619 | ||||||
| chr9:115069622
|
C | T | 18 | a0008c0005t0001g0084a0008c0005t0001g0085a0008c0005t0001g0086others(15): Show | 18 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.3214+3981G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069622 | ||||||
| chr9:115069626
|
C | G | 1 | a0004c0004t0002g0325 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3214+3977G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069626 | ||||||
| chr9:115069626
|
C | T | 1 | a0015c0029t0003g0010 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3214+3977G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069626 | ||||||
| chr9:115069626
|
CCCTCCCT others(93): Show |
C | 3 | a0003c0035t0004g0150a0003c0035t0004g0151a0003c0077t0004g0356 | 3 | HG02559.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3214+3877_3214+397 others(104): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069626 | ||||||
| chr9:115069630
|
C | T | 48 | a0001c0002t0001g0138a0001c0002t0001g0141a0001c0002t0001g0142others(45): Show | 48 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.3214+3973G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069630 | ||||||
| chr9:115069630
|
CCCTCCCT others(85): Show |
C | 10 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(7): Show | 11 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3214+3881_3214+397 others(96): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069630 | ||||||
| chr9:115069634
|
C | T | 31 | a0001c0009t0001g0155a0001c0009t0001g0160a0001c0009t0001g0188others(28): Show | 31 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.3214+3969G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069634 | ||||||
| chr9:115069634
|
CCCTCCCT others(85): Show |
C | 1 | a0004c0018t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3214+3877_3214+396 others(96): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069634 | ||||||
| chr9:115069638
|
C | T | 1 | a0008c0005t0001g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3214+3965G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069638 | ||||||
| chr9:115069638
|
CCCTTCCT others(89): Show |
C | 1 | a0005c0017t0002g0079 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3214+3869_3214+396 others(100): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069638 | ||||||
| chr9:115069642
|
T | C | 99 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.3214+3961A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069642 | ||||||
| chr9:115069642
|
T | TCCTCCCT others(5): Show |
1 | a0002c0001t0002g0002 | 2 | NA19066.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.3214+3949_3214+396 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069642 | ||||||
| chr9:115069642
|
T | TCCTCCCT others(9): Show |
7 | a0002c0001t0002g0169a0002c0001t0002g0185a0004c0004t0002g0293others(4): Show | 7 | HG00642.hp1 HG03704.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.3214+3945_3214+396 others(20): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069642 | ||||||
| chr9:115069646
|
C | T | 1 | a0036c0087t0003g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3214+3957G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069646 | ||||||
| chr9:115069647
|
C | T | 1 | a0010c0008t0001g0077 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3214+3956G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069647 | ||||||
| chr9:115069650
|
C | T | 1 | a0053c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3214+3953G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069650 | ||||||
| chr9:115069654
|
C | CCCTCCCT others(25): Show |
24 | a0002c0001t0002g0100a0002c0001t0002g0157a0002c0001t0002g0168others(21): Show | 24 | HG00558.hp1 HG00733.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.3214+3948_3214+394 others(36): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | ||||||
| chr9:115069654
|
C | CCCTCCCT others(21): Show |
4 | a0002c0001t0002g0154a0002c0001t0007g0018a0007c0006t0007g0035others(1): Show | 4 | HG02602.hp1 HG02886.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.3214+3948_3214+394 others(32): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | ||||||
| chr9:115069654
|
C | CCCTCCCT others(17): Show |
1 | a0002c0001t0001g0165 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3214+3948_3214+394 others(28): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | ||||||
| chr9:115069654
|
C | CCCTCCCT others(5): Show |
16 | a0002c0001t0002g0082a0002c0001t0002g0094a0002c0001t0002g0096others(13): Show | 16 | HG00408.hp2 HG01358.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.3214+3948_3214+394 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | ||||||
| chr9:115069654
|
C | T | 3 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321 | 3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3214+3949G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | ||||||
| chr9:115069654
|
CCCTCCCT others(65): Show |
C | 6 | a0001c0002t0008g0136a0001c0002t0008g0139a0001c0011t0008g0111others(3): Show | 6 | HG01361.hp1 HG04184.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.3214+3877_3214+394 others(76): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | ||||||
| chr9:115069654
|
CCCTCCCT others(73): Show |
C | 11 | a0001c0002t0001g0134a0001c0011t0001g0114a0002c0093t0004g0122others(8): Show | 11 | HG00621.hp1 HG01891.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.3214+3869_3214+394 others(84): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069654 | ||||||
| chr9:115069658
|
C | T | 8 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(5): Show | 8 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3214+3945G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069658 | ||||||
| chr9:115069658
|
CCCTCCCT others(69): Show |
C | 10 | a0001c0002t0001g0138a0001c0002t0001g0141a0001c0002t0001g0142others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.3214+3869_3214+394 others(80): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069658 | ||||||
| chr9:115069662
|
C | CCCTCCCT others(73): Show |
1 | a0009c0100t0005g0318 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3214+3940_3214+394 others(84): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069662 | ||||||
| chr9:115069662
|
C | T | 73 | a0002c0001t0002g0092a0002c0001t0002g0098a0002c0001t0002g0110others(70): Show | 74 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.3214+3941G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069662 | ||||||
| chr9:115069662
|
CCCTCCCT others(1): Show |
C | 29 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(26): Show | 29 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.3214+3933_3214+394 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069662 | ||||||
| chr9:115069662
|
CCCTCCCT others(57): Show |
C | 1 | a0053c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3214+3877_3214+394 others(68): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069662 | ||||||
| chr9:115069662
|
CCCTCCCT others(65): Show |
C | 2 | a0023c0033t0001g0126a0023c0033t0001g0127 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3214+3869_3214+394 others(76): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069662 | ||||||
| chr9:115069666
|
C | T | 78 | a0001c0009t0001g0101a0001c0009t0001g0178a0001c0009t0001g0244others(75): Show | 79 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.3214+3937G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069666 | ||||||
| chr9:115069666
|
CCCTT | C | 19 | a0001c0002t0001g0305a0001c0002t0008g0144a0001c0011t0001g0095others(16): Show | 19 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.3214+3933_3214+393 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069666 | ||||||
| chr9:115069666
|
CCCTTCCT others(49): Show |
C | 1 | a0007c0041t0007g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3214+3881_3214+393 others(60): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069666 | ||||||
| chr9:115069666
|
CCCTTCCT others(53): Show |
C | 22 | a0005c0014t0001g0005a0005c0014t0001g0304a0005c0014t0001g0308others(19): Show | 23 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.3214+3877_3214+393 others(64): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069666 | ||||||
| chr9:115069666
|
CCCTTCCT others(61): Show |
C | 1 | a0023c0033t0001g0338 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3214+3869_3214+393 others(72): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069666 | ||||||
| chr9:115069670
|
T | C | 77 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0178others(74): Show | 78 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.3214+3933A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069670 | ||||||
| chr9:115069670
|
TCCTC | T | 3 | a0003c0003t0001g0309a0003c0055t0001g0238a0015c0040t0003g0040 | 3 | NA18961.hp1 NA19007.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.3214+3929_3214+393 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069670 | ||||||
| chr9:115069670
|
TCCTCCCT others(25): Show |
T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3214+3901_3214+393 others(36): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069670 | ||||||
| chr9:115069670
|
TCCTCCCT others(29): Show |
T | 1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3214+3897_3214+393 others(40): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069670 | ||||||
| chr9:115069670
|
TCCTCCCT others(73): Show |
T | 1 | a0046c0053t0018g0245 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3214+3853_3214+393 others(84): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069670 | ||||||
| chr9:115069674
|
C | T | 70 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(67): Show | 71 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.3214+3929G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069674 | ||||||
| chr9:115069678
|
C | T | 29 | a0002c0001t0002g0092a0002c0001t0002g0098a0002c0001t0002g0110others(26): Show | 29 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.3214+3925G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069678 | ||||||
| chr9:115069678
|
CCCTCCCT others(49): Show |
C | 2 | a0005c0014t0001g0289a0005c0034t0002g0198 | 2 | HG01109.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.3214+3869_3214+392 others(60): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069678 | ||||||
| chr9:115069679
|
C | CCTCCCTT others(1): Show |
3 | a0003c0003t0004g0337a0027c0070t0002g0351a0052c0057t0014g0346 | 3 | HG02280.hp2 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3214+3923_3214+392 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069679 | ||||||
| chr9:115069679
|
C | CCTTG | 3 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321 | 3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3214+3923_3214+392 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069679 | ||||||
| chr9:115069682
|
C | T | 24 | a0001c0002t0001g0305a0001c0002t0008g0144a0001c0094t0008g0176others(21): Show | 24 | HG00099.hp2 HG01070.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.3214+3921G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069682 | ||||||
| chr9:115069682
|
CCCTCCCT others(45): Show |
C | 3 | a0005c0023t0001g0299a0005c0023t0001g0300a0005c0023t0018g0361 | 3 | HG00099.hp1 HG00323.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.3214+3869_3214+392 others(56): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069682 | ||||||
| chr9:115069686
|
C | T | 68 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(65): Show | 70 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.3214+3917G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069686 | ||||||
| chr9:115069686
|
CCCTCCCT others(33): Show |
C | 1 | a0003c0003t0019g0360 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3214+3877_3214+391 others(44): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069686 | ||||||
| chr9:115069686
|
CCCTCCCT others(41): Show |
C | 2 | a0004c0051t0004g0342a0005c0023t0001g0314 | 2 | HG04228.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3214+3869_3214+391 others(52): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069686 | ||||||
| chr9:115069690
|
C | T | 16 | a0001c0009t0001g0123a0001c0009t0001g0244a0002c0001t0002g0179others(13): Show | 16 | HG01070.hp1 HG01175.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.3214+3913G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069690 | ||||||
| chr9:115069690
|
CCCTCCCT others(37): Show |
C | 4 | a0004c0075t0004g0266a0034c0060t0014g0253a0049c0064t0014g0343others(1): Show | 4 | HG00738.hp1 HG02257.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3214+3869_3214+391 others(48): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069690 | ||||||
| chr9:115069694
|
C | T | 70 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0178others(67): Show | 70 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.3214+3909G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069694 | ||||||
| chr9:115069694
|
CCCTCCCT others(33): Show |
C | 2 | a0004c0018t0004g0334a0006c0007t0005g0204 | 2 | HG02698.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3214+3869_3214+390 others(44): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069694 | ||||||
| chr9:115069695
|
C | T | 51 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(48): Show | 52 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.3214+3908G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069695 | ||||||
| chr9:115069698
|
C | CCCTTCCT others(29): Show |
3 | a0007c0006t0007g0001a0007c0006t0007g0051a0007c0006t0016g0050 | 4 | NA19000.hp1 NA19004.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.3214+3904_3214+390 others(40): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069698 | ||||||
| chr9:115069698
|
C | T | 81 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(78): Show | 81 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.3214+3905G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069698 | ||||||
| chr9:115069699
|
C | T | 1 | a0036c0087t0003g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3214+3904G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069699 | ||||||
| chr9:115069702
|
C | CCCTCCCT others(69): Show |
1 | a0002c0001t0002g0195 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3214+3900_3214+390 others(80): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069702 | ||||||
| chr9:115069702
|
C | CCCTCCCT others(9): Show |
2 | a0002c0001t0002g0191a0051c0097t0002g0186 | 2 | HG03654.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.3214+3885_3214+390 others(20): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069702 | ||||||
| chr9:115069702
|
C | CCCTTCCT others(29): Show |
4 | a0002c0001t0002g0179a0002c0001t0002g0180a0002c0001t0002g0184others(1): Show | 4 | HG01175.hp2 HG01192.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.3214+3900_3214+390 others(40): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069702 | ||||||
| chr9:115069702
|
C | T | 114 | a0001c0009t0001g0101a0001c0009t0001g0155a0001c0009t0001g0160others(111): Show | 114 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.3214+3901G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069702 | ||||||
| chr9:115069702
|
CCCTCCCT others(25): Show |
C | 24 | a0006c0007t0005g0221a0006c0007t0005g0222a0006c0007t0005g0270others(21): Show | 25 | HG00621.hp2 HG01074.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.3214+3869_3214+390 others(36): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069702 | ||||||
| chr9:115069706
|
C | T | 60 | a0001c0002t0008g0144a0001c0009t0001g0155a0001c0009t0001g0160others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.3214+3897G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069706 | ||||||
| chr9:115069706
|
CCCTTCCT others(21): Show |
C | 28 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(25): Show | 28 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.3214+3869_3214+389 others(32): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069706 | ||||||
| chr9:115069710
|
T | C | 39 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(36): Show | 39 | HG01070.hp1 HG01175.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.3214+3893A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069710 | ||||||
| chr9:115069710
|
TCCTTCCT others(37): Show |
T | 3 | a0005c0034t0002g0197a0005c0067t0002g0359a0009c0092t0002g0093 | 3 | HG01243.hp2 HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3214+3849_3214+389 others(48): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069710 | ||||||
| chr9:115069714
|
T | C | 54 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(51): Show | 54 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.3214+3889A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069714 | ||||||
| chr9:115069714
|
T | TCCTC | 3 | a0002c0001t0001g0104a0004c0004t0002g0210a0004c0045t0002g0230 | 3 | HG01928.hp2 NA18965.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.3214+3888_3214+388 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069714 | ||||||
| chr9:115069714
|
T | TCCTTCCT others(1): Show |
10 | a0002c0001t0002g0002a0002c0001t0002g0159a0002c0001t0002g0169others(7): Show | 11 | HG00642.hp1 HG02109.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.3214+3888_3214+388 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069714 | ||||||
| chr9:115069714
|
T | TCCTTCCT others(61): Show |
2 | a0017c0022t0004g0252a0017c0022t0004g0261 | 2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3214+3888_3214+388 others(72): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069714 | ||||||
| chr9:115069718
|
T | C | 56 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(53): Show | 56 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.3214+3885A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069718 | ||||||
| chr9:115069718
|
TCCTTCCT others(25): Show |
T | 2 | a0008c0005t0001g0115a0011c0010t0001g0302 | 2 | HG00099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.3214+3853_3214+388 others(36): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069718 | ||||||
| chr9:115069718
|
TCCTTCCT others(49): Show |
T | 2 | a0001c0002t0001g0305a0004c0018t0004g0213 | 2 | HG01358.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3214+3829_3214+388 others(60): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069718 | ||||||
| chr9:115069722
|
T | C | 45 | a0001c0009t0001g0155a0001c0009t0001g0160a0001c0009t0001g0188others(42): Show | 45 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.3214+3881A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069722 | ||||||
| chr9:115069722
|
TCCTTCCT others(13): Show |
T | 1 | a0029c0046t0004g0340 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3214+3861_3214+388 others(24): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069722 | ||||||
| chr9:115069722
|
TCCTTCCT others(17): Show |
T | 1 | a0029c0046t0004g0339 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3214+3857_3214+388 others(28): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069722 | ||||||
| chr9:115069722
|
TCCTTCCT others(21): Show |
T | 7 | a0011c0010t0001g0064a0011c0010t0001g0227a0011c0010t0001g0228others(4): Show | 7 | HG02258.hp1 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.3214+3853_3214+388 others(32): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069722 | ||||||
| chr9:115069722
|
TCCTTCCT others(45): Show |
T | 27 | a0001c0002t0001g0267a0001c0002t0001g0268a0001c0002t0001g0275others(24): Show | 27 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.3214+3829_3214+388 others(56): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069722 | ||||||
| chr9:115069726
|
T | C | 39 | a0001c0009t0001g0160a0001c0024t0003g0008a0001c0024t0003g0009others(36): Show | 40 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.3214+3877A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069726 | ||||||
| chr9:115069726
|
TCCTCCCT others(13): Show |
T | 3 | a0008c0005t0001g0121a0039c0090t0001g0116a0044c0065t0005g0326 | 3 | HG01070.hp1 HG02109.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3214+3857_3214+387 others(24): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069726 | ||||||
| chr9:115069726
|
TCCTCCCT others(17): Show |
T | 5 | a0011c0010t0001g0209a0011c0076t0001g0206a0022c0025t0001g0347others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.3214+3853_3214+387 others(28): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069726 | ||||||
| chr9:115069726
|
TCCTCCCT others(41): Show |
T | 6 | a0001c0002t0001g0128a0001c0002t0001g0322a0001c0002t0001g0323others(3): Show | 6 | HG01099.hp1 HG02698.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3214+3829_3214+387 others(52): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069726 | ||||||
| chr9:115069730
|
C | T | 74 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(71): Show | 76 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.3214+3873G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069730 | ||||||
| chr9:115069734
|
T | C | 27 | a0003c0055t0001g0238a0004c0018t0004g0226a0004c0050t0014g0345others(24): Show | 29 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.3214+3869A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069734 | ||||||
| chr9:115069734
|
T | TCCTC | 3 | a0002c0096t0002g0156a0004c0004t0001g0269a0007c0006t0007g0043 | 3 | HG03834.hp1 NA18944.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.3214+3865_3214+386 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069734 | ||||||
| chr9:115069734
|
TCCTCCCT others(1): Show |
T | 13 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0178others(10): Show | 13 | HG01261.hp2 HG01981.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.3214+3861_3214+386 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069734 | ||||||
| chr9:115069734
|
TCCTCCCT others(33): Show |
T | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3214+3829_3214+386 others(44): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069734 | ||||||
| chr9:115069735
|
C | T | 1 | a0006c0007t0005g0204 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3214+3868G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069735 | ||||||
| chr9:115069738
|
C | CCCTT | 24 | a0002c0001t0001g0104a0002c0001t0002g0002a0002c0001t0002g0092others(21): Show | 25 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.3214+3864_3214+386 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069738 | ||||||
| chr9:115069738
|
C | CCCTTCCT others(57): Show |
1 | a0017c0022t0004g0130 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3214+3864_3214+386 others(68): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069738 | ||||||
| chr9:115069738
|
C | T | 57 | a0001c0002t0001g0138a0001c0002t0001g0141a0001c0002t0001g0142others(54): Show | 57 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.3214+3865G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069738 | ||||||
| chr9:115069739
|
C | T | 1 | a0055c0079t0023g0194 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3214+3864G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069739 | ||||||
| chr9:115069742
|
C | T | 48 | a0001c0002t0001g0306a0001c0002t0010g0330a0001c0009t0001g0155others(45): Show | 48 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.3214+3861G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069742 | ||||||
| chr9:115069746
|
C | CCCTCCCT others(57): Show |
1 | a0017c0022t0004g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3214+3856_3214+385 others(68): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069746 | ||||||
| chr9:115069746
|
C | T | 40 | a0001c0009t0001g0101a0001c0009t0010g0107a0001c0011t0001g0114others(37): Show | 40 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.3214+3857G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069746 | ||||||
| chr9:115069750
|
C | CCCTTCCT others(21): Show |
6 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3214+3852_3214+385 others(32): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069750 | ||||||
| chr9:115069750
|
C | T | 50 | a0004c0051t0004g0342a0005c0014t0001g0005a0005c0014t0001g0304others(47): Show | 51 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.3214+3853G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069750 | ||||||
| chr9:115069754
|
C | T | 65 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(62): Show | 66 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.3214+3849G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069754 | ||||||
| chr9:115069758
|
C | T | 23 | a0001c0002t0008g0136a0001c0002t0008g0139a0001c0011t0008g0111others(20): Show | 24 | HG01081.hp2 HG01099.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.3214+3845G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069758 | ||||||
| chr9:115069762
|
C | T | 46 | a0001c0002t0001g0138a0001c0002t0001g0141a0001c0002t0001g0142others(43): Show | 46 | HG00621.hp1 HG01175.hp1 HG01261.hp2 others(43): Show |
intron_variant | MODIFIER | c.3214+3841G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069762 | ||||||
| chr9:115069766
|
C | T | 73 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(70): Show | 73 | HG00621.hp1 HG00738.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.3214+3837G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069766 | ||||||
| chr9:115069770
|
C | T | 115 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.3214+3833G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069770 | ||||||
| chr9:115069774
|
C | CCCTTCCT others(25): Show |
1 | a0052c0057t0014g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3214+3828_3214+382 others(36): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069774 | ||||||
| chr9:115069774
|
C | T | 164 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.3214+3829G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069774 | ||||||
| chr9:115069778
|
T | C | 3 | a0002c0001t0002g0002a0005c0017t0002g0079a0053c0104t0028g0341 | 4 | HG02145.hp1 HG03017.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.3214+3825A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069778 | ||||||
| chr9:115069798
|
T | C | 5 | a0020c0030t0009g0048a0020c0030t0009g0049a0029c0046t0004g0340others(2): Show | 5 | HG02886.hp1 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.3214+3805A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069798 | ||||||
| chr9:115069802
|
C | T | 3 | a0020c0030t0009g0048a0020c0030t0009g0049a0029c0046t0004g0340 | 3 | HG03471.hp2 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3214+3801G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069802 | ||||||
| chr9:115069806
|
T | C | 3 | a0020c0030t0009g0048a0020c0030t0009g0049a0029c0046t0004g0340 | 3 | HG03471.hp2 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3214+3797A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069806 | ||||||
| chr9:115069884
|
G | A | 1 | a0005c0014t0001g0289 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3214+3719C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069884 | ||||||
| chr9:115069897
|
T | C | 1 | a0014c0016t0006g0073 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3214+3706A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069897 | ||||||
| chr9:115069943
|
G | A | 1 | a0001c0094t0008g0176 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3214+3660C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115069943 | ||||||
| chr9:115070012
|
C | T | 4 | a0002c0001t0002g0168a0002c0020t0011g0132a0004c0004t0002g0220others(1): Show | 4 | NA18954.hp2 NA18961.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.3214+3591G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070012 | ||||||
| chr9:115070046
|
G | A | 1 | a0036c0087t0003g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3214+3557C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070046 | ||||||
| chr9:115070073
|
C | T | 7 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3214+3530G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070073 | ||||||
| chr9:115070087
|
A | G | 110 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(107): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.3214+3516T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070087 | ||||||
| chr9:115070137
|
T | C | 110 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(107): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.3214+3466A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070137 | ||||||
| chr9:115070158
|
A | G | 1 | a0005c0037t0004g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3214+3445T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070158 | ||||||
| chr9:115070332
|
C | A | 1 | a0053c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3214+3271G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070332 | ||||||
| chr9:115070339
|
G | C | 117 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.3214+3264C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070339 | ||||||
| chr9:115070384
|
A | C | 270 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(267): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.3214+3219T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070384 | ||||||
| chr9:115070491
|
G | A | 1 | a0007c0006t0017g0012 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.3214+3112C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070491 | ||||||
| chr9:115070522
|
C | T | 4 | a0004c0004t0002g0325a0022c0025t0001g0347a0022c0025t0001g0348others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3214+3081G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070522 | ||||||
| chr9:115070553
|
T | C | 1 | a0011c0010t0001g0302 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3214+3050A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070553 | ||||||
| chr9:115070696
|
G | A | 37 | a0008c0005t0001g0083a0008c0005t0001g0084a0008c0005t0001g0085others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.3214+2907C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070696 | ||||||
| chr9:115070696
|
G | T | 53 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(50): Show | 53 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.3214+2907C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070696 | ||||||
| chr9:115070824
|
C | A | 2 | a0001c0002t0001g0306a0001c0002t0010g0330 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3214+2779G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070824 | ||||||
| chr9:115070827
|
G | A | 270 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(267): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.3214+2776C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070827 | ||||||
| chr9:115070945
|
G | A | 2 | a0001c0011t0001g0114a0046c0053t0018g0245 | 2 | HG00323.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.3214+2658C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070945 | ||||||
| chr9:115070997
|
C | T | 1 | a0003c0003t0019g0273 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3214+2606G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115070997 | ||||||
| chr9:115071212
|
G | A | 117 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.3214+2391C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071212 | ||||||
| chr9:115071214
|
G | A | 1 | a0009c0100t0005g0318 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3214+2389C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071214 | ||||||
| chr9:115071239
|
A | G | 117 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.3214+2364T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071239 | ||||||
| chr9:115071266
|
T | C | 1 | a0008c0005t0001g0102 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3214+2337A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071266 | ||||||
| chr9:115071352
|
C | T | 117 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.3214+2251G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071352 | ||||||
| chr9:115071356
|
A | G | 2 | a0023c0033t0001g0127a0023c0033t0001g0338 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.3214+2247T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071356 | ||||||
| chr9:115071400
|
T | G | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3214+2203A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071400 | ||||||
| chr9:115071428
|
T | C | 117 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.3214+2175A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071428 | ||||||
| chr9:115071524
|
T | G | 1 | a0013c0059t0002g0067 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3214+2079A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071524 | ||||||
| chr9:115071564
|
A | C | 117 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.3214+2039T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071564 | ||||||
| chr9:115071574
|
T | C | 117 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.3214+2029A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071574 | ||||||
| chr9:115071691
|
A | G | 117 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.3214+1912T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071691 | ||||||
| chr9:115071711
|
G | A | 22 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(19): Show | 22 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.3214+1892C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071711 | ||||||
| chr9:115071747
|
A | G | 15 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(12): Show | 16 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.3214+1856T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071747 | ||||||
| chr9:115071767
|
A | G | 1 | a0010c0008t0003g0013 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3214+1836T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071767 | ||||||
| chr9:115071783
|
C | T | 53 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(50): Show | 53 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.3214+1820G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071783 | ||||||
| chr9:115071786
|
T | G | 3 | a0005c0034t0002g0197a0005c0034t0002g0198a0005c0067t0002g0359 | 3 | HG01109.hp2 HG01243.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3214+1817A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071786 | ||||||
| chr9:115071791
|
C | T | 270 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(267): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.3214+1812G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071791 | ||||||
| chr9:115071854
|
T | C | 7 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3214+1749A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115071854 | ||||||
| chr9:115072112
|
C | T | 5 | a0005c0034t0002g0197a0005c0034t0002g0198a0005c0067t0002g0359others(2): Show | 5 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.3214+1491G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072112 | ||||||
| chr9:115072214
|
G | A | 22 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(19): Show | 22 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.3214+1389C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072214 | ||||||
| chr9:115072561
|
C | T | 117 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.3214+1042G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072561 | ||||||
| chr9:115072651
|
C | T | 5 | a0009c0100t0005g0318a0017c0022t0004g0130a0017c0022t0004g0131others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3214+952G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072651 | ||||||
| chr9:115072652
|
G | A | 53 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(50): Show | 53 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.3214+951C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072652 | ||||||
| chr9:115072674
|
A | G | 24 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(21): Show | 24 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.3214+929T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072674 | ||||||
| chr9:115072817
|
A | T | 15 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(12): Show | 16 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.3214+786T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072817 | ||||||
| chr9:115072902
|
C | T | 2 | a0004c0050t0014g0345a0005c0062t0026g0250 | 2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3214+701G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072902 | ||||||
| chr9:115072935
|
C | G | 240 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.3214+668G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072935 | ||||||
| chr9:115072943
|
T | G | 240 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.3214+660A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072943 | ||||||
| chr9:115072975
|
A | G | 51 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(48): Show | 51 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.3214+628T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072975 | ||||||
| chr9:115072997
|
A | G | 270 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(267): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.3214+606T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115072997 | ||||||
| chr9:115073019
|
G | A | 3 | a0007c0006t0007g0001a0007c0006t0007g0051a0007c0006t0016g0050 | 4 | NA19000.hp1 NA19004.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.3214+584C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115073019 | ||||||
| chr9:115073150
|
A | G | 1 | a0002c0001t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3214+453T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115073150 | ||||||
| chr9:115073322
|
A | G | 3 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321 | 3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3214+281T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115073322 | ||||||
| chr9:115073428
|
A | G | 5 | a0009c0100t0005g0318a0017c0022t0004g0130a0017c0022t0004g0131others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3214+175T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115073428 | ||||||
| chr9:115073525
|
G | C | 1 | a0004c0004t0002g0297 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3214+78C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 10/27 | chr9 | 115073525 | ||||||
| chr9:115073909
|
A | G | 270 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(267): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2951-43T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115073909 | ||||||
| chr9:115074121
|
G | A | 117 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2951-255C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074121 | ||||||
| chr9:115074166
|
A | G | 1 | a0002c0096t0002g0156 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2951-300T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074166 | ||||||
| chr9:115074180
|
A | C | 1 | a0053c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2951-314T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074180 | ||||||
| chr9:115074294
|
C | G | 1 | a0046c0053t0018g0245 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2951-428G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074294 | ||||||
| chr9:115074297
|
A | G | 6 | a0005c0037t0004g0152a0005c0037t0004g0271a0013c0021t0004g0129others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2951-431T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074297 | ||||||
| chr9:115074533
|
AG | A | 4 | a0018c0028t0012g0258a0018c0028t0012g0259a0018c0028t0012g0260others(1): Show | 4 | HG01496.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2951-668delC | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074533 | ||||||
| chr9:115074768
|
CAT | C | 15 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(12): Show | 16 | HG01081.hp2 HG01099.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.2951-904_2951-903d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074768 | ||||||
| chr9:115074805
|
C | T | 23 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(20): Show | 23 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.2951-939G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074805 | ||||||
| chr9:115074863
|
C | T | 5 | a0009c0100t0005g0318a0017c0022t0004g0130a0017c0022t0004g0131others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2951-997G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074863 | ||||||
| chr9:115074918
|
C | T | 2 | a0004c0050t0014g0345a0005c0062t0026g0250 | 2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2951-1052G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074918 | ||||||
| chr9:115074969
|
C | A | 1 | a0011c0010t0001g0265 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2950+1063G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074969 | ||||||
| chr9:115074973
|
A | G | 101 | a0001c0009t0001g0123a0001c0009t0001g0155a0001c0009t0001g0160others(98): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.2950+1059T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115074973 | ||||||
| chr9:115075042
|
G | A | 3 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321 | 3 | HG02647.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2950+990C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075042 | ||||||
| chr9:115075111
|
T | G | 2 | a0001c0009t0001g0188a0003c0003t0010g0328 | 2 | HG01515.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2950+921A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075111 | ||||||
| chr9:115075240
|
A | G | 1 | a0053c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2950+792T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075240 | ||||||
| chr9:115075432
|
A | C | 1 | a0011c0010t0001g0265 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2950+600T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075432 | ||||||
| chr9:115075552
|
C | G | 1 | a0002c0001t0002g0100 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2950+480G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075552 | ||||||
| chr9:115075561
|
C | T | 7 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2950+471G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075561 | ||||||
| chr9:115075579
|
G | A | 1 | a0034c0060t0014g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2950+453C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075579 | ||||||
| chr9:115075678
|
G | A | 2 | a0004c0050t0014g0345a0005c0062t0026g0250 | 2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2950+354C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075678 | ||||||
| chr9:115075717
|
G | A | 25 | a0005c0014t0001g0005a0005c0014t0001g0289a0005c0014t0001g0304others(22): Show | 26 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2950+315C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075717 | ||||||
| chr9:115075814
|
C | T | 117 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2950+218G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075814 | ||||||
| chr9:115075894
|
T | C | 3 | a0004c0018t0004g0224a0024c0083t0001g0056a0027c0071t0001g0355 | 3 | HG01109.hp1 HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2950+138A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075894 | ||||||
| chr9:115075987
|
G | C | 1 | a0004c0004t0002g0325 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2950+45C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075987 | ||||||
| chr9:115075995
|
C | G | 5 | a0009c0100t0005g0318a0017c0022t0004g0130a0017c0022t0004g0131others(2): Show | 5 | HG02647.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2950+37G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 9/27 | chr9 | 115075995 | ||||||
| chr9:115076345
|
C | G | 53 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(50): Show | 53 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.2860+45G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 8/27 | chr9 | 115076345 | ||||||
| chr9:115076661
|
G | A | 7 | a0001c0009t0015g0124a0001c0009t0015g0350a0001c0024t0015g0321others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2675-86C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076661 | ||||||
| chr9:115076724
|
T | C | 2 | a0002c0001t0002g0100a0002c0020t0002g0148 | 2 | NA18747.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2675-149A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076724 | ||||||
| chr9:115076736
|
C | A | 2 | a0004c0050t0014g0345a0005c0062t0026g0250 | 2 | HG01192.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2675-161G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076736 | ||||||
| chr9:115076779
|
C | T | 7 | a0002c0093t0004g0122a0004c0018t0004g0213a0004c0018t0004g0224others(4): Show | 7 | HG02145.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2675-204G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076779 | ||||||
| chr9:115076780
|
G | A | 1 | a0009c0100t0005g0318 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2675-205C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076780 | ||||||
| chr9:115076823
|
G | T | 1 | a0002c0001t0002g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2675-248C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076823 | ||||||
| chr9:115076948
|
A | G | 5 | a0005c0034t0002g0197a0005c0034t0002g0198a0005c0067t0002g0359others(2): Show | 5 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2675-373T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115076948 | ||||||
| chr9:115077110
|
A | C | 2 | a0029c0046t0004g0339a0029c0046t0004g0340 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2675-535T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077110 | ||||||
| chr9:115077111
|
A | G | 1 | a0002c0020t0001g0145 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2675-536T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077111 | ||||||
| chr9:115077152
|
T | C | 1 | a0007c0006t0007g0006 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2675-577A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077152 | ||||||
| chr9:115077194
|
A | T | 1 | a0009c0092t0002g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2675-619T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077194 | ||||||
| chr9:115077257
|
T | C | 1 | a0011c0010t0001g0225 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2675-682A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077257 | ||||||
| chr9:115077269
|
A | G | 90 | a0001c0009t0001g0101a0002c0001t0002g0092a0002c0001t0002g0110others(87): Show | 91 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.2674+674T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077269 | ||||||
| chr9:115077278
|
A | G | 1 | a0004c0004t0002g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2674+665T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077278 | ||||||
| chr9:115077297
|
T | C | 26 | a0001c0009t0001g0188a0001c0009t0002g0117a0002c0001t0002g0169others(23): Show | 27 | HG00280.hp1 HG00642.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.2674+646A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077297 | ||||||
| chr9:115077299
|
G | A | 1 | a0045c0049t0002g0242 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2674+644C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077299 | ||||||
| chr9:115077299
|
GC | G | 17 | a0008c0005t0001g0083a0008c0005t0001g0084a0008c0005t0001g0085others(14): Show | 17 | HG00140.hp2 HG00642.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.2674+643delG | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077299 | ||||||
| chr9:115077303
|
G | A | 1 | a0008c0005t0001g0196 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2674+640C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077303 | ||||||
| chr9:115077336
|
G | A | 1 | a0001c0011t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2674+607C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077336 | ||||||
| chr9:115077338
|
G | C | 98 | a0001c0002t0001g0276a0001c0009t0001g0101a0001c0009t0001g0123others(95): Show | 99 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.2674+605C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077338 | ||||||
| chr9:115077479
|
C | T | 38 | a0002c0098t0002g0147a0004c0004t0001g0269a0004c0051t0004g0342others(35): Show | 39 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.2674+464G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077479 | ||||||
| chr9:115077482
|
G | T | 16 | a0001c0009t0001g0188a0005c0017t0001g0081a0005c0017t0002g0076others(13): Show | 17 | HG01081.hp2 HG01257.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2674+461C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077482 | ||||||
| chr9:115077483
|
C | T | 1 | a0006c0007t0005g0324 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2674+460G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077483 | ||||||
| chr9:115077518
|
A | G | 31 | a0004c0004t0001g0269a0007c0006t0003g0028a0007c0006t0003g0052others(28): Show | 32 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.2674+425T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077518 | ||||||
| chr9:115077589
|
G | A | 33 | a0002c0098t0002g0147a0004c0004t0001g0269a0004c0051t0004g0342others(30): Show | 33 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.2674+354C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077589 | ||||||
| chr9:115077606
|
G | A | 1 | a0008c0005t0001g0196 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2674+337C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077606 | ||||||
| chr9:115077782
|
A | G | 105 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2674+161T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 7/27 | chr9 | 115077782 | ||||||
| chr9:115078422
|
T | C | 13 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(10): Show | 13 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2405-210A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115078422 | ||||||
| chr9:115078463
|
G | C | 150 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(147): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2405-251C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115078463 | ||||||
| chr9:115078482
|
G | T | 1 | a0054c0080t0003g0047 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2405-270C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115078482 | ||||||
| chr9:115078496
|
A | C | 1 | a0019c0026t0006g0068 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2405-284T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115078496 | ||||||
| chr9:115078505
|
G | A | 1 | a0003c0003t0001g0332 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2405-293C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115078505 | ||||||
| chr9:115078558
|
A | T | 152 | a0001c0002t0001g0192a0001c0009t0001g0101a0001c0009t0001g0123others(149): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2405-346T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115078558 | ||||||
| chr9:115078643
|
A | G | 124 | a0001c0002t0001g0192a0001c0009t0001g0101a0001c0009t0001g0123others(121): Show | 127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.2405-431T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115078643 | ||||||
| chr9:115079049
|
G | GA | 3 | a0001c0002t0001g0134a0001c0002t0013g0135a0002c0020t0002g0148 | 3 | HG02071.hp1 NA18747.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.2405-838dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079049 | ||||||
| chr9:115079137
|
T | C | 34 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(31): Show | 34 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.2405-925A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079137 | ||||||
| chr9:115079291
|
G | T | 355 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(352): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.2405-1079C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079291 | ||||||
| chr9:115079623
|
G | C | 355 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(352): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.2405-1411C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079623 | ||||||
| chr9:115079635
|
T | C | 1 | a0005c0066t0002g0251 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2405-1423A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079635 | ||||||
| chr9:115079659
|
C | T | 43 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(40): Show | 43 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.2405-1447G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079659 | ||||||
| chr9:115079694
|
C | T | 19 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(16): Show | 19 | HG02015.hp2 HG02129.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.2405-1482G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079694 | ||||||
| chr9:115079994
|
C | T | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2404+1778G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115079994 | ||||||
| chr9:115080006
|
A | T | 9 | a0009c0092t0002g0093a0012c0012t0006g0057a0012c0012t0006g0058others(6): Show | 9 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.2404+1766T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080006 | ||||||
| chr9:115080028
|
A | G | 216 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(213): Show | 218 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.2404+1744T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080028 | ||||||
| chr9:115080114
|
A | G | 6 | a0008c0005t0001g0083a0008c0005t0001g0084a0008c0005t0001g0085others(3): Show | 6 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2404+1658T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080114 | ||||||
| chr9:115080190
|
A | G | 3 | a0005c0067t0002g0359a0006c0007t0005g0357a0030c0047t0001g0358 | 3 | HG02280.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2404+1582T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080190 | ||||||
| chr9:115080259
|
C | G | 3 | a0029c0046t0004g0339a0029c0046t0004g0340a0053c0104t0028g0341 | 3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2404+1513G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080259 | ||||||
| chr9:115080260
|
A | T | 3 | a0029c0046t0004g0339a0029c0046t0004g0340a0053c0104t0028g0341 | 3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2404+1512T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080260 | ||||||
| chr9:115080320
|
T | TG | 215 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(212): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.2404+1451dupC | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080320 | ||||||
| chr9:115080322
|
A | T | 1 | a0022c0025t0001g0347 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2404+1450T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080322 | ||||||
| chr9:115080327
|
T | C | 1 | a0001c0002t0010g0288 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2404+1445A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080327 | ||||||
| chr9:115080367
|
G | A | 1 | a0004c0018t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2404+1405C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080367 | ||||||
| chr9:115080442
|
T | C | 3 | a0002c0020t0002g0065a0002c0020t0002g0249a0016c0101t0005g0066 | 3 | NA18995.hp1 NA19078.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2404+1330A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080442 | ||||||
| chr9:115080545
|
C | T | 1 | a0044c0065t0005g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2404+1227G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080545 | ||||||
| chr9:115080648
|
C | T | 3 | a0004c0073t0002g0274a0004c0074t0002g0286a0004c0075t0004g0266 | 3 | HG00738.hp1 HG02055.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2404+1124G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080648 | ||||||
| chr9:115080658
|
C | T | 3 | a0005c0037t0004g0152a0005c0037t0004g0271a0044c0065t0005g0326 | 3 | HG02109.hp2 HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2404+1114G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080658 | ||||||
| chr9:115080848
|
A | G | 360 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(357): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.2404+924T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080848 | ||||||
| chr9:115080895
|
G | GA | 52 | a0001c0002t0013g0135a0002c0001t0002g0154a0002c0001t0002g0175others(49): Show | 53 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.2404+876dupT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080895 | ||||||
| chr9:115080895
|
GA | G | 121 | a0001c0002t0010g0330a0001c0009t0001g0188a0001c0009t0002g0117others(118): Show | 122 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.2404+876delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115080895 | ||||||
| chr9:115081143
|
C | T | 1 | a0010c0008t0003g0013 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2404+629G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115081143 | ||||||
| chr9:115081385
|
G | A | 1 | a0003c0003t0001g0332 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2404+387C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115081385 | ||||||
| chr9:115081442
|
G | A | 1 | a0002c0001t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2404+330C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115081442 | ||||||
| chr9:115081635
|
C | T | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2404+137G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115081635 | ||||||
| chr9:115081653
|
A | T | 8 | a0012c0012t0006g0057a0012c0012t0006g0058a0012c0012t0006g0059others(5): Show | 8 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.2404+119T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115081653 | ||||||
| chr9:115081741
|
T | C | 3 | a0005c0067t0002g0359a0006c0007t0005g0357a0030c0047t0001g0358 | 3 | HG02280.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2404+31A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 6/27 | chr9 | 115081741 | ||||||
| chr9:115081960
|
G | A | 170 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(167): Show | 172 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.2248-32C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115081960 | ||||||
| chr9:115081965
|
G | T | 1 | a0002c0001t0002g0110 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2248-37C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115081965 | ||||||
| chr9:115082236
|
C | G | 1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2248-308G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082236 | ||||||
| chr9:115082247
|
G | A | 2 | a0001c0002t0001g0306a0001c0002t0010g0330 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2248-319C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082247 | ||||||
| chr9:115082372
|
C | A | 1 | a0002c0001t0002g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2247+320G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082372 | ||||||
| chr9:115082492
|
G | C | 204 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(201): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2247+200C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082492 | ||||||
| chr9:115082532
|
A | G | 6 | a0005c0034t0002g0197a0005c0034t0002g0198a0023c0033t0001g0126others(3): Show | 6 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.2247+160T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082532 | ||||||
| chr9:115082568
|
C | T | 1 | a0002c0001t0002g0100 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2247+124G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082568 | ||||||
| chr9:115082578
|
C | A | 1 | a0005c0037t0004g0152 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2247+114G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082578 | ||||||
| chr9:115082584
|
C | T | 1 | a0006c0015t0005g0235 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2247+108G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082584 | ||||||
| chr9:115082654
|
C | T | 11 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2247+38G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 5/27 | chr9 | 115082654 | ||||||
| chr9:115082866
|
C | T | 1 | a0001c0002t0008g0144 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2132-59G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115082866 | ||||||
| chr9:115082887
|
A | G | 1 | a0009c0031t0001g0166 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2132-80T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115082887 | ||||||
| chr9:115083046
|
C | T | 45 | a0002c0001t0007g0018a0007c0006t0003g0028a0007c0006t0003g0052others(42): Show | 46 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.2132-239G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083046 | ||||||
| chr9:115083047
|
G | A | 1 | a0052c0057t0014g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2132-240C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083047 | ||||||
| chr9:115083054
|
T | G | 201 | a0001c0002t0001g0128a0001c0002t0001g0138a0001c0002t0001g0141others(198): Show | 203 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2132-247A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083054 | ||||||
| chr9:115083068
|
A | G | 15 | a0013c0021t0004g0129a0013c0021t0004g0254a0013c0021t0004g0255others(12): Show | 15 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.2132-261T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083068 | ||||||
| chr9:115083124
|
G | A | 205 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(202): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.2132-317C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083124 | ||||||
| chr9:115083162
|
G | A | 163 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(160): Show | 165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2132-355C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083162 | ||||||
| chr9:115083170
|
G | A | 163 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(160): Show | 165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2132-363C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083170 | ||||||
| chr9:115083183
|
GA | G | 15 | a0013c0021t0004g0129a0013c0021t0004g0254a0013c0021t0004g0255others(12): Show | 15 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.2132-377delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083183 | ||||||
| chr9:115083310
|
C | T | 1 | a0053c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2132-503G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083310 | ||||||
| chr9:115083332
|
A | G | 43 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(40): Show | 43 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.2132-525T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083332 | ||||||
| chr9:115083380
|
C | T | 163 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(160): Show | 165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2132-573G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083380 | ||||||
| chr9:115083507
|
G | A | 1 | a0005c0066t0002g0251 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2132-700C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083507 | ||||||
| chr9:115083602
|
C | CT | 59 | a0001c0002t0013g0135a0001c0009t0001g0101a0002c0001t0007g0018others(56): Show | 60 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.2131+606dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083602 | ||||||
| chr9:115083602
|
CT | C | 150 | a0001c0002t0010g0330a0001c0024t0003g0008a0002c0020t0011g0132others(147): Show | 152 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.2131+606delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083602 | ||||||
| chr9:115083602
|
CTT | C | 17 | a0003c0035t0004g0150a0003c0035t0004g0151a0003c0055t0001g0238others(14): Show | 17 | HG01192.hp1 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2131+605_2131+606d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083602 | ||||||
| chr9:115083638
|
A | C | 163 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(160): Show | 165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2131+571T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083638 | ||||||
| chr9:115083801
|
C | T | 135 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(132): Show | 137 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.2131+408G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083801 | ||||||
| chr9:115083837
|
C | T | 163 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(160): Show | 165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2131+372G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115083837 | ||||||
| chr9:115084140
|
C | T | 1 | a0001c0011t0001g0161 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2131+69G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115084140 | ||||||
| chr9:115084171
|
A | G | 208 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(205): Show | 210 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.2131+38T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 4/27 | chr9 | 115084171 | ||||||
| chr9:115084577
|
G | A | 1 | a0006c0015t0002g0241 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1868-105C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115084577 | ||||||
| chr9:115084701
|
C | G | 164 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(161): Show | 166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1868-229G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115084701 | ||||||
| chr9:115084706
|
G | T | 164 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(161): Show | 166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1868-234C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115084706 | ||||||
| chr9:115084771
|
A | T | 3 | a0023c0033t0001g0126a0023c0033t0001g0127a0023c0033t0001g0338 | 3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1868-299T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115084771 | ||||||
| chr9:115084874
|
A | T | 355 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(352): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1868-402T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115084874 | ||||||
| chr9:115084900
|
C | A | 355 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(352): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1868-428G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115084900 | ||||||
| chr9:115085054
|
A | G | 1 | a0003c0027t0002g0215 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1868-582T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085054 | ||||||
| chr9:115085241
|
C | G | 1 | a0028c0038t0005g0354 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1867+623G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085241 | ||||||
| chr9:115085334
|
C | G | 164 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(161): Show | 166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1867+530G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085334 | ||||||
| chr9:115085429
|
G | A | 2 | a0003c0003t0001g0199a0006c0007t0005g0200 | 2 | NA19000.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1867+435C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085429 | ||||||
| chr9:115085590
|
T | C | 355 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(352): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1867+274A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085590 | ||||||
| chr9:115085676
|
C | T | 1 | a0019c0026t0006g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1867+188G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085676 | ||||||
| chr9:115085688
|
G | A | 2 | a0004c0004t0002g0280a0004c0004t0002g0281 | 2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1867+176C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085688 | ||||||
| chr9:115085790
|
C | T | 1 | a0006c0015t0002g0241 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1867+74G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085790 | ||||||
| chr9:115085833
|
A | T | 113 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(110): Show | 114 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1867+31T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085833 | ||||||
| chr9:115085850
|
G | T | 1 | a0015c0040t0003g0040 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1867+14C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 3/27 | chr9 | 115085850 | ||||||
| chr9:115087362
|
T | G | 151 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(148): Show | 153 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.458-89A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087362 | ||||||
| chr9:115087387
|
C | G | 44 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.458-114G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087387 | ||||||
| chr9:115087401
|
A | G | 4 | a0001c0002t0013g0135a0002c0020t0002g0065a0002c0020t0002g0249others(1): Show | 4 | NA18995.hp1 NA19078.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-128T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087401 | ||||||
| chr9:115087412
|
G | A | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.458-139C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087412 | ||||||
| chr9:115087443
|
C | G | 42 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(39): Show | 42 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.458-170G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087443 | ||||||
| chr9:115087471
|
T | C | 12 | a0009c0092t0002g0093a0012c0012t0006g0057a0012c0012t0006g0058others(9): Show | 12 | HG02145.hp1 HG02630.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.458-198A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087471 | ||||||
| chr9:115087507
|
A | T | 1 | a0002c0001t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.458-234T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087507 | ||||||
| chr9:115087527
|
G | GATGTGT | 5 | a0001c0002t0001g0128a0009c0100t0005g0318a0021c0032t0001g0317others(2): Show | 5 | HG01123.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-255_458-254ins others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | ||||||
| chr9:115087527
|
G | GGTGT | 8 | a0001c0002t0001g0306a0001c0002t0008g0137a0001c0002t0008g0144others(5): Show | 8 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-258_458-255dup others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | ||||||
| chr9:115087527
|
G | GGTGTGT | 36 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(33): Show | 36 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.458-260_458-255dup others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | ||||||
| chr9:115087527
|
G | GGTGTGTG others(1): Show |
36 | a0001c0002t0001g0298a0001c0002t0013g0135a0001c0024t0001g0133others(33): Show | 37 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.458-262_458-255dup others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | ||||||
| chr9:115087527
|
G | GGTGTGTG others(3): Show |
3 | a0007c0041t0016g0031a0010c0008t0001g0077a0010c0008t0003g0013 | 3 | HG00597.hp2 HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.458-264_458-255dup others(10): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | ||||||
| chr9:115087527
|
G | GGTGTGTG others(5): Show |
4 | a0007c0006t0007g0019a0007c0041t0007g0030a0016c0043t0009g0016others(1): Show | 4 | HG00408.hp2 HG04184.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-266_458-255dup others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | ||||||
| chr9:115087527
|
G | GGTGTGTG others(7): Show |
1 | a0002c0001t0007g0018 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.458-268_458-255dup others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | ||||||
| chr9:115087527
|
G | GTGTGTGT others(6): Show |
1 | a0007c0006t0007g0006 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.458-255_458-254ins others(13): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | ||||||
| chr9:115087527
|
GGT | G | 4 | a0002c0001t0002g0099a0002c0001t0002g0109a0002c0001t0002g0170others(1): Show | 4 | HG02071.hp2 NA18959.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-256_458-255del others(2): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | ||||||
| chr9:115087527
|
GGTGT | G | 25 | a0001c0009t0001g0155a0001c0009t0001g0160a0001c0009t0001g0178others(22): Show | 26 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.458-258_458-255del others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | ||||||
| chr9:115087527
|
GGTGTGT | G | 64 | a0001c0002t0001g0192a0001c0009t0001g0101a0001c0009t0001g0123others(61): Show | 65 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.458-260_458-255del others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | ||||||
| chr9:115087527
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0002t0001g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.458-264_458-255del others(10): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | ||||||
| chr9:115087527
|
GGTGTGTG others(17): Show |
G | 162 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(159): Show | 164 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.458-278_458-255del others(24): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087527 | ||||||
| chr9:115087528
|
G | A | 2 | a0001c0002t0001g0322a0001c0002t0001g0323 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.458-255C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087528 | ||||||
| chr9:115087581
|
G | A | 1 | a0007c0086t0020g0044 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.458-308C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087581 | ||||||
| chr9:115087583
|
G | A | 2 | a0005c0034t0002g0197a0005c0034t0002g0198 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.458-310C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087583 | ||||||
| chr9:115087698
|
C | CT | 54 | a0001c0002t0001g0192a0001c0009t0001g0155a0001c0009t0001g0160others(51): Show | 55 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.458-426dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087698 | ||||||
| chr9:115087698
|
CT | C | 49 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(46): Show | 49 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.458-426delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087698 | ||||||
| chr9:115087698
|
CTT | C | 153 | a0001c0002t0001g0142a0001c0002t0001g0305a0001c0002t0010g0330others(150): Show | 155 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.458-427_458-426del others(2): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087698 | ||||||
| chr9:115087702
|
T | TC | 43 | a0002c0001t0007g0018a0007c0006t0003g0028a0007c0006t0003g0052others(40): Show | 44 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.458-430_458-429ins others(1): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087702 | ||||||
| chr9:115087703
|
T | C | 1 | a0004c0004t0002g0220 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.458-430A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087703 | ||||||
| chr9:115087703
|
T | TC | 45 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0244others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.458-431_458-430ins others(1): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087703 | ||||||
| chr9:115087704
|
T | C | 2 | a0003c0003t0001g0279a0005c0062t0026g0250 | 2 | HG01175.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.458-431A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087704 | ||||||
| chr9:115087705
|
T | C | 125 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(122): Show | 127 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.458-432A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087705 | ||||||
| chr9:115087842
|
C | T | 1 | a0014c0016t0006g0069 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.458-569G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087842 | ||||||
| chr9:115087846
|
C | T | 1 | a0001c0009t0001g0101 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.458-573G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087846 | ||||||
| chr9:115087862
|
C | T | 9 | a0013c0059t0002g0067a0014c0016t0006g0069a0014c0016t0006g0071others(6): Show | 9 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-589G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087862 | ||||||
| chr9:115087925
|
A | C | 1 | a0002c0001t0002g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.458-652T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115087925 | ||||||
| chr9:115088005
|
T | C | 3 | a0029c0046t0004g0339a0029c0046t0004g0340a0053c0104t0028g0341 | 3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.458-732A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088005 | ||||||
| chr9:115088024
|
T | C | 1 | a0011c0076t0001g0206 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.458-751A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088024 | ||||||
| chr9:115088205
|
T | C | 1 | a0002c0001t0002g0099 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.458-932A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088205 | ||||||
| chr9:115088283
|
G | T | 44 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.458-1010C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088283 | ||||||
| chr9:115088303
|
G | A | 3 | a0029c0046t0004g0339a0029c0046t0004g0340a0053c0104t0028g0341 | 3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.458-1030C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088303 | ||||||
| chr9:115088322
|
A | G | 1 | a0007c0006t0007g0045 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.458-1049T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088322 | ||||||
| chr9:115088427
|
T | C | 1 | a0005c0017t0002g0078 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.458-1154A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088427 | ||||||
| chr9:115088442
|
C | T | 1 | a0005c0034t0002g0198 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.458-1169G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088442 | ||||||
| chr9:115088612
|
A | G | 1 | a0039c0090t0001g0116 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.458-1339T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088612 | ||||||
| chr9:115088625
|
T | A | 1 | a0028c0038t0005g0354 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.458-1352A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088625 | ||||||
| chr9:115088702
|
A | T | 1 | a0003c0003t0001g0199 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.458-1429T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088702 | ||||||
| chr9:115088751
|
T | C | 3 | a0029c0046t0004g0339a0029c0046t0004g0340a0053c0104t0028g0341 | 3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.458-1478A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115088751 | ||||||
| chr9:115089018
|
T | C | 5 | a0017c0022t0004g0130a0017c0022t0004g0131a0017c0022t0004g0252others(2): Show | 5 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.457+1544A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089018 | ||||||
| chr9:115089159
|
G | T | 1 | a0049c0064t0014g0343 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.457+1403C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089159 | ||||||
| chr9:115089185
|
A | G | 2 | a0003c0035t0004g0150a0003c0035t0004g0151 | 2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.457+1377T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089185 | ||||||
| chr9:115089210
|
C | T | 46 | a0002c0001t0007g0018a0007c0006t0003g0028a0007c0006t0003g0052others(43): Show | 47 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.457+1352G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089210 | ||||||
| chr9:115089393
|
T | C | 163 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(160): Show | 165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.457+1169A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089393 | ||||||
| chr9:115089478
|
A | ATC | 11 | a0001c0002t0003g0007a0001c0011t0001g0095a0002c0001t0001g0104others(8): Show | 12 | HG02015.hp1 HG02071.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.457+1082_457+1083d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089478 | ||||||
| chr9:115089478
|
ATC | A | 82 | a0003c0003t0001g0229a0003c0003t0001g0239a0003c0003t0001g0240others(79): Show | 83 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.457+1082_457+1083d others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089478 | ||||||
| chr9:115089478
|
ATCTC | A | 79 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(76): Show | 80 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.457+1080_457+1083d others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089478 | ||||||
| chr9:115089484
|
C | A | 3 | a0022c0025t0001g0347a0022c0025t0001g0348a0022c0025t0001g0349 | 3 | HG01243.hp1 HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.457+1078G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089484 | ||||||
| chr9:115089593
|
C | T | 1 | a0009c0092t0002g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.457+969G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089593 | ||||||
| chr9:115089891
|
T | C | 43 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(40): Show | 43 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.457+671A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089891 | ||||||
| chr9:115089960
|
C | A | 9 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(6): Show | 9 | HG02257.hp1 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.457+602G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115089960 | ||||||
| chr9:115090190
|
C | T | 1 | a0001c0002t0010g0288 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.457+372G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115090190 | ||||||
| chr9:115090209
|
T | A | 1 | a0003c0003t0004g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.457+353A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115090209 | ||||||
| chr9:115090235
|
A | G | 1 | a0019c0026t0006g0068 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.457+327T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115090235 | ||||||
| chr9:115090243
|
T | C | 113 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(110): Show | 114 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.457+319A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115090243 | ||||||
| chr9:115090325
|
G | T | 1 | a0001c0002t0001g0267 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.457+237C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115090325 | ||||||
| chr9:115090398
|
C | T | 2 | a0001c0024t0001g0133a0002c0020t0011g0132 | 2 | NA18982.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.457+164G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 2/27 | chr9 | 115090398 | ||||||
| chr9:115091353
|
C | T | 45 | a0002c0001t0007g0018a0007c0006t0003g0028a0007c0006t0003g0052others(42): Show | 46 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.-136-199G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115091353 | ||||||
| chr9:115092027
|
G | A | 13 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(10): Show | 13 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136-873C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092027 | ||||||
| chr9:115092123
|
T | G | 3 | a0029c0046t0004g0339a0029c0046t0004g0340a0053c0104t0028g0341 | 3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-136-969A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092123 | ||||||
| chr9:115092387
|
G | A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-136-1233C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092387 | ||||||
| chr9:115092569
|
A | G | 3 | a0022c0025t0001g0347a0022c0025t0001g0348a0022c0025t0001g0349 | 3 | HG01243.hp1 HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-136-1415T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092569 | ||||||
| chr9:115092642
|
T | C | 355 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(352): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-136-1488A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092642 | ||||||
| chr9:115092670
|
T | C | 3 | a0022c0025t0001g0347a0022c0025t0001g0348a0022c0025t0001g0349 | 3 | HG01243.hp1 HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-136-1516A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092670 | ||||||
| chr9:115092720
|
C | T | 1 | a0018c0028t0012g0258 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-136-1566G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092720 | ||||||
| chr9:115092749
|
A | AT | 51 | a0001c0002t0008g0136a0002c0001t0007g0018a0002c0098t0002g0147others(48): Show | 52 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.-136-1596dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092749 | ||||||
| chr9:115092749
|
AT | A | 143 | a0001c0002t0010g0330a0002c0001t0002g0109a0003c0003t0001g0199others(140): Show | 144 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.-136-1596delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092749 | ||||||
| chr9:115092749
|
ATT | A | 15 | a0003c0027t0002g0215a0003c0052t0001g0234a0003c0055t0001g0238others(12): Show | 16 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-136-1597_-136-159 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092749 | ||||||
| chr9:115092755
|
T | A | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-136-1601A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092755 | ||||||
| chr9:115092908
|
A | G | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-136-1754T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115092908 | ||||||
| chr9:115093164
|
T | C | 7 | a0001c0011t0008g0111a0002c0001t0002g0092a0002c0001t0002g0098others(4): Show | 7 | HG01169.hp1 HG01361.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136-2010A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093164 | ||||||
| chr9:115093192
|
A | C | 8 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(5): Show | 8 | NA18952.hp2 NA18993.hp1 NA19000.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-2038T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093192 | ||||||
| chr9:115093228
|
G | C | 149 | a0002c0098t0002g0147a0003c0003t0001g0199a0003c0003t0001g0207others(146): Show | 151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.-136-2074C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093228 | ||||||
| chr9:115093620
|
C | CT | 54 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0192others(51): Show | 54 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.-136-2467dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093620 | ||||||
| chr9:115093620
|
CT | C | 6 | a0003c0003t0001g0329a0005c0062t0026g0250a0008c0005t0001g0102others(3): Show | 6 | HG01099.hp2 HG01192.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136-2467delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093620 | ||||||
| chr9:115093648
|
A | G | 1 | a0001c0009t0001g0101 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-136-2494T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093648 | ||||||
| chr9:115093765
|
A | T | 355 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(352): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-136-2611T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093765 | ||||||
| chr9:115093832
|
G | A | 3 | a0029c0046t0004g0339a0029c0046t0004g0340a0053c0104t0028g0341 | 3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-136-2678C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093832 | ||||||
| chr9:115093835
|
A | C | 207 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(204): Show | 209 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.-136-2681T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093835 | ||||||
| chr9:115093851
|
T | G | 13 | a0003c0052t0001g0234a0003c0055t0001g0238a0004c0045t0002g0230others(10): Show | 14 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-136-2697A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093851 | ||||||
| chr9:115093861
|
T | C | 43 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(40): Show | 43 | HG00140.hp1 HG00280.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.-136-2707A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093861 | ||||||
| chr9:115093865
|
G | C | 13 | a0003c0052t0001g0234a0003c0055t0001g0238a0004c0045t0002g0230others(10): Show | 14 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-136-2711C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093865 | ||||||
| chr9:115093915
|
G | A | 1 | a0010c0008t0001g0077 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-136-2761C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115093915 | ||||||
| chr9:115094025
|
A | G | 9 | a0009c0092t0002g0093a0012c0012t0006g0057a0012c0012t0006g0058others(6): Show | 9 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-2871T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094025 | ||||||
| chr9:115094039
|
C | T | 211 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(208): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.-136-2885G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094039 | ||||||
| chr9:115094144
|
T | C | 1 | a0002c0001t0006g0120 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-136-2990A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094144 | ||||||
| chr9:115094203
|
T | C | 1 | a0013c0059t0002g0067 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-136-3049A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094203 | ||||||
| chr9:115094205
|
C | T | 2 | a0001c0009t0001g0155a0001c0009t0001g0160 | 2 | NA18939.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-136-3051G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094205 | ||||||
| chr9:115094207
|
C | A | 32 | a0003c0052t0001g0234a0003c0055t0001g0238a0004c0045t0002g0230others(29): Show | 33 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.-136-3053G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094207 | ||||||
| chr9:115094214
|
G | A | 11 | a0013c0059t0002g0067a0014c0016t0006g0069a0014c0016t0006g0071others(8): Show | 11 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.-136-3060C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094214 | ||||||
| chr9:115094273
|
A | G | 1 | a0001c0002t0003g0007 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-136-3119T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094273 | ||||||
| chr9:115094275
|
C | T | 89 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(86): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-136-3121G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094275 | ||||||
| chr9:115094518
|
G | A | 5 | a0003c0077t0004g0356a0013c0021t0004g0129a0013c0021t0004g0254others(2): Show | 5 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136-3364C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094518 | ||||||
| chr9:115094598
|
G | A | 151 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(148): Show | 152 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-136-3444C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094598 | ||||||
| chr9:115094633
|
A | T | 176 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(173): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.-136-3479T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094633 | ||||||
| chr9:115094639
|
T | C | 1 | a0001c0009t0001g0123 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-136-3485A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094639 | ||||||
| chr9:115094814
|
CCT | C | 64 | a0001c0002t0008g0144a0001c0002t0013g0135a0002c0001t0002g0158others(61): Show | 65 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-136-3662_-136-366 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094814 | ||||||
| chr9:115094814
|
CCTCTGTG others(3): Show |
C | 7 | a0014c0016t0006g0069a0014c0016t0006g0074a0019c0026t0006g0068others(4): Show | 7 | HG00642.hp2 HG00741.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136-3670_-136-366 others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094814 | ||||||
| chr9:115094814
|
CCTCTGTG others(5): Show |
C | 6 | a0013c0059t0002g0067a0014c0016t0006g0071a0014c0016t0006g0072others(3): Show | 6 | HG01346.hp1 HG01884.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-3672_-136-366 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094814 | ||||||
| chr9:115094814
|
CCTCTGTG others(7): Show |
C | 5 | a0004c0051t0004g0342a0005c0034t0002g0197a0005c0034t0002g0198others(2): Show | 5 | HG01109.hp2 HG01243.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-3674_-136-366 others(18): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094814 | ||||||
| chr9:115094814
|
CCTCTGTG others(11): Show |
C | 1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-136-3678_-136-366 others(22): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094814 | ||||||
| chr9:115094814
|
CCTCTGTG others(13): Show |
C | 14 | a0001c0009t0001g0244a0003c0052t0001g0234a0003c0055t0001g0238others(11): Show | 15 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-136-3680_-136-366 others(24): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094814 | ||||||
| chr9:115094815
|
CTCTG | C | 67 | a0001c0002t0001g0128a0001c0002t0001g0192a0001c0002t0001g0267others(64): Show | 68 | HG00280.hp2 HG00597.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.-136-3665_-136-366 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094815 | ||||||
| chr9:115094815
|
CTCTGTG | C | 95 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(92): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.-136-3667_-136-366 others(10): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094815 | ||||||
| chr9:115094815
|
CTCTGTGT others(1): Show |
C | 22 | a0001c0002t0001g0268a0001c0002t0001g0306a0001c0002t0010g0330others(19): Show | 22 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-136-3669_-136-366 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094815 | ||||||
| chr9:115094815
|
CTCTGTGT others(3): Show |
C | 10 | a0001c0009t0001g0123a0002c0001t0002g0113a0002c0001t0002g0170others(7): Show | 10 | HG02071.hp2 HG02257.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136-3671_-136-366 others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094815 | ||||||
| chr9:115094815
|
CTCTGTGT others(5): Show |
C | 4 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0062t0026g0250others(1): Show | 4 | HG01192.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-3673_-136-366 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094815 | ||||||
| chr9:115094815
|
CTCTGTGT others(9): Show |
C | 10 | a0004c0004t0002g0307a0009c0092t0002g0093a0012c0012t0006g0057others(7): Show | 10 | HG01978.hp1 HG02630.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-136-3677_-136-366 others(20): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094815 | ||||||
| chr9:115094817
|
C | G | 50 | a0001c0002t0001g0290a0001c0009t0015g0350a0002c0001t0001g0104others(47): Show | 50 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.-136-3663G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094817 | ||||||
| chr9:115094867
|
G | C | 332 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(329): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-136-3713C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094867 | ||||||
| chr9:115094867
|
G | GTC | 15 | a0002c0001t0001g0104a0003c0003t0001g0216a0004c0004t0002g0205others(12): Show | 15 | HG00558.hp1 HG01496.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.-136-3714_-136-371 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094867 | ||||||
| chr9:115094867
|
G | GTGTC | 9 | a0003c0077t0004g0356a0007c0006t0007g0037a0007c0006t0017g0039others(6): Show | 9 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.-136-3714_-136-371 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115094867 | ||||||
| chr9:115095208
|
A | G | 346 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(343): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.-136-4054T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095208 | ||||||
| chr9:115095210
|
G | A | 88 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(85): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-136-4056C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095210 | ||||||
| chr9:115095211
|
C | T | 142 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(139): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-136-4057G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095211 | ||||||
| chr9:115095212
|
G | A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-136-4058C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095212 | ||||||
| chr9:115095437
|
G | A | 3 | a0022c0025t0001g0347a0022c0025t0001g0348a0022c0025t0001g0349 | 3 | HG01243.hp1 HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-136-4283C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095437 | ||||||
| chr9:115095444
|
GTGTATAT others(207): Show |
G | 45 | a0001c0009t0001g0244a0003c0003t0001g0229a0003c0003t0001g0239others(42): Show | 46 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.-136-4504_-136-429 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095444 | ||||||
| chr9:115095446
|
G | GTA | 3 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257 | 3 | HG02559.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-136-4294_-136-429 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095446 | ||||||
| chr9:115095448
|
ATATATAT others(173): Show |
A | 5 | a0002c0001t0002g0169a0002c0001t0002g0184a0002c0001t0002g0185others(2): Show | 5 | HG00280.hp1 HG00642.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-4474_-136-429 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095448 | ||||||
| chr9:115095450
|
ATATATAT others(151): Show |
A | 41 | a0001c0002t0001g0192a0001c0009t0001g0101a0001c0009t0001g0155others(38): Show | 42 | HG00733.hp2 HG01081.hp2 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.-136-4454_-136-429 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095450 | ||||||
| chr9:115095450
|
ATATATAT others(225): Show |
A | 2 | a0002c0098t0002g0147a0009c0099t0001g0146 | 2 | HG02071.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-136-4528_-136-429 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095450 | ||||||
| chr9:115095452
|
ATATATGT others(149): Show |
A | 5 | a0005c0062t0026g0250a0022c0025t0001g0347a0022c0025t0001g0348others(2): Show | 5 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136-4454_-136-429 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095452 | ||||||
| chr9:115095472
|
ATATATAT others(129): Show |
A | 1 | a0002c0001t0002g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-136-4454_-136-431 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095472 | ||||||
| chr9:115095472
|
ATATATAT others(215): Show |
A | 23 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(20): Show | 23 | HG02071.hp1 HG02080.hp2 HG02698.hp2 others(20): Show |
intron_variant | MODIFIER | c.-136-4540_-136-431 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095472 | ||||||
| chr9:115095480
|
G | GTA | 6 | a0017c0022t0004g0252a0017c0022t0004g0261a0029c0046t0004g0339others(3): Show | 6 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-4328_-136-432 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095480 | ||||||
| chr9:115095482
|
A | G | 1 | a0027c0070t0002g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-136-4328T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095482 | ||||||
| chr9:115095482
|
ATATATAT others(3): Show |
A | 2 | a0010c0008t0003g0026a0010c0008t0021g0011 | 2 | NA18972.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-136-4338_-136-432 others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095482 | ||||||
| chr9:115095482
|
ATATATAT others(205): Show |
A | 2 | a0004c0004t0002g0325a0004c0018t0004g0213 | 2 | HG04115.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-136-4540_-136-432 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095482 | ||||||
| chr9:115095494
|
ATATATAT others(193): Show |
A | 131 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-136-4540_-136-434 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095494 | ||||||
| chr9:115095496
|
ATATATGT others(105): Show |
A | 2 | a0003c0035t0004g0150a0003c0035t0004g0151 | 2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-136-4454_-136-434 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095496 | ||||||
| chr9:115095496
|
ATATATGT others(191): Show |
A | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-136-4540_-136-434 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095496 | ||||||
| chr9:115095502
|
G | A | 1 | a0005c0061t0002g0257 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-136-4348C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095502 | ||||||
| chr9:115095502
|
GTATATAT others(109): Show |
G | 1 | a0008c0005t0001g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-136-4464_-136-434 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095502 | ||||||
| chr9:115095502
|
GTATATAT others(153): Show |
G | 41 | a0001c0009t0001g0123a0001c0009t0002g0117a0001c0009t0010g0107others(38): Show | 42 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.-136-4508_-136-434 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095502 | ||||||
| chr9:115095504
|
A | G | 1 | a0005c0061t0002g0257 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-136-4350T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095504 | ||||||
| chr9:115095510
|
ATATGTAT others(143): Show |
A | 40 | a0002c0001t0007g0018a0007c0006t0003g0028a0007c0006t0003g0052others(37): Show | 41 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.-136-4506_-136-435 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095510 | ||||||
| chr9:115095514
|
GTATATAT others(119): Show |
G | 3 | a0029c0046t0004g0339a0029c0046t0004g0340a0053c0104t0028g0341 | 3 | HG02145.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-136-4486_-136-436 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095514 | ||||||
| chr9:115095516
|
ATATATAT others(171): Show |
A | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-136-4540_-136-436 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095516 | ||||||
| chr9:115095524
|
GTA | G | 3 | a0017c0022t0004g0252a0017c0022t0004g0261a0050c0063t0012g0149 | 3 | HG02647.hp1 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-4372_-136-437 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095524 | ||||||
| chr9:115095524
|
GTATATAT others(131): Show |
G | 1 | a0055c0079t0023g0194 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136-4508_-136-437 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095524 | ||||||
| chr9:115095524
|
GTATATAT others(153): Show |
G | 1 | a0009c0019t0011g0193 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-136-4530_-136-437 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095524 | ||||||
| chr9:115095532
|
ATATGTAT others(143): Show |
A | 1 | a0010c0008t0003g0034 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-136-4528_-136-437 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095532 | ||||||
| chr9:115095532
|
ATATGTAT others(165): Show |
A | 1 | a0051c0097t0002g0186 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-136-4550_-136-437 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095532 | ||||||
| chr9:115095536
|
G | GTATATAT others(5): Show |
1 | a0018c0028t0012g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-136-4394_-136-438 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095536 | ||||||
| chr9:115095538
|
ATATATAT others(105): Show |
A | 1 | a0005c0061t0002g0257 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-136-4496_-136-438 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095538 | ||||||
| chr9:115095548
|
ATATATAT others(149): Show |
A | 1 | a0002c0001t0002g0191 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-136-4550_-136-439 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095548 | ||||||
| chr9:115095556
|
GTATATAT others(99): Show |
G | 2 | a0010c0008t0003g0026a0010c0008t0021g0011 | 2 | NA18972.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-136-4508_-136-440 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095556 | ||||||
| chr9:115095568
|
ATATATAT others(119): Show |
A | 3 | a0017c0022t0004g0252a0017c0022t0004g0261a0050c0063t0012g0149 | 3 | HG02647.hp1 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-4540_-136-441 others(4): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095568 | ||||||
| chr9:115095576
|
G | GTATATAT others(47): Show |
2 | a0018c0028t0012g0258a0018c0028t0012g0259 | 2 | HG01496.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-136-4423_-136-442 others(58): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095576 | ||||||
| chr9:115095598
|
ATATATAT others(3): Show |
A | 1 | a0024c0082t0004g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-136-4454_-136-444 others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095598 | ||||||
| chr9:115095606
|
A | G | 1 | a0024c0083t0001g0056 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-136-4452T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095606 | ||||||
| chr9:115095608
|
G | A | 1 | a0024c0083t0001g0056 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-136-4454C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095608 | ||||||
| chr9:115095608
|
G | GTA | 3 | a0018c0028t0012g0258a0018c0028t0012g0259a0018c0028t0012g0260 | 3 | HG01496.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-136-4456_-136-445 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095608 | ||||||
| chr9:115095640
|
A | ATATATAT others(35): Show |
1 | a0018c0028t0012g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-136-4528_-136-448 others(46): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095640 | ||||||
| chr9:115095650
|
G | GTA | 7 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0062t0026g0250others(4): Show | 7 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136-4498_-136-449 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095650 | ||||||
| chr9:115095662
|
A | G | 40 | a0002c0001t0007g0018a0007c0006t0003g0028a0007c0006t0003g0052others(37): Show | 41 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.-136-4508T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095662 | ||||||
| chr9:115095670
|
A | G | 3 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257 | 3 | HG02559.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-136-4516T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095670 | ||||||
| chr9:115095671
|
T | C | 11 | a0013c0059t0002g0067a0014c0016t0006g0069a0014c0016t0006g0071others(8): Show | 11 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.-136-4517A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095671 | ||||||
| chr9:115095672
|
G | A | 3 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257 | 3 | HG02559.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-136-4518C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095672 | ||||||
| chr9:115095684
|
A | G | 1 | a0010c0008t0003g0034 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-136-4530T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095684 | ||||||
| chr9:115095692
|
A | G | 5 | a0002c0098t0002g0147a0009c0099t0001g0146a0029c0046t0004g0339others(2): Show | 5 | HG02071.hp2 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-4538T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095692 | ||||||
| chr9:115095694
|
G | A | 5 | a0002c0098t0002g0147a0009c0099t0001g0146a0029c0046t0004g0339others(2): Show | 5 | HG02071.hp2 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-4540C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095694 | ||||||
| chr9:115095702
|
A | G | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-136-4548T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095702 | ||||||
| chr9:115095704
|
G | A | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-136-4550C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095704 | ||||||
| chr9:115095749
|
A | G | 2 | a0005c0034t0002g0197a0005c0034t0002g0198 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-136-4595T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095749 | ||||||
| chr9:115095787
|
T | A | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136-4633A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095787 | ||||||
| chr9:115095866
|
G | A | 14 | a0003c0003t0001g0247a0003c0003t0001g0283a0003c0003t0001g0309others(11): Show | 14 | HG00423.hp1 HG00597.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-136-4712C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115095866 | ||||||
| chr9:115096019
|
G | A | 8 | a0010c0008t0003g0023a0010c0008t0003g0026a0010c0008t0003g0027others(5): Show | 8 | NA18942.hp1 NA18956.hp1 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136-4865C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096019 | ||||||
| chr9:115096481
|
G | A | 6 | a0017c0022t0004g0252a0017c0022t0004g0261a0029c0046t0004g0339others(3): Show | 6 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-5327C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096481 | ||||||
| chr9:115096486
|
C | T | 1 | a0004c0004t0002g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-136-5332G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096486 | ||||||
| chr9:115096597
|
G | A | 8 | a0009c0092t0002g0093a0012c0012t0006g0057a0012c0012t0006g0058others(5): Show | 8 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-5443C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096597 | ||||||
| chr9:115096626
|
GA | G | 134 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(131): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.-136-5473delT | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096626 | ||||||
| chr9:115096638
|
A | G | 1 | a0008c0005t0001g0115 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-136-5484T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096638 | ||||||
| chr9:115096663
|
C | A | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136-5509G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096663 | ||||||
| chr9:115096717
|
T | C | 1 | a0001c0011t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-136-5563A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096717 | ||||||
| chr9:115096989
|
G | A | 7 | a0004c0051t0004g0342a0005c0034t0002g0197a0005c0034t0002g0198others(4): Show | 7 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136-5835C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115096989 | ||||||
| chr9:115097006
|
A | G | 8 | a0009c0092t0002g0093a0012c0012t0006g0057a0012c0012t0006g0058others(5): Show | 8 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-5852T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097006 | ||||||
| chr9:115097019
|
G | A | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-136-5865C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097019 | ||||||
| chr9:115097261
|
G | T | 6 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(3): Show | 6 | HG01346.hp2 HG03017.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136-6107C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097261 | ||||||
| chr9:115097362
|
G | A | 46 | a0002c0001t0007g0018a0007c0006t0003g0028a0007c0006t0003g0052others(43): Show | 47 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-136-6208C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097362 | ||||||
| chr9:115097616
|
G | A | 1 | a0006c0007t0005g0270 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-136-6462C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097616 | ||||||
| chr9:115097668
|
G | T | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136-6514C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097668 | ||||||
| chr9:115097796
|
G | C | 1 | a0006c0007t0024g0212 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-136-6642C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097796 | ||||||
| chr9:115097992
|
A | G | 2 | a0005c0017t0002g0079a0005c0066t0002g0251 | 2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-136-6838T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115097992 | ||||||
| chr9:115098016
|
C | T | 138 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-136-6862G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098016 | ||||||
| chr9:115098169
|
A | C | 5 | a0001c0009t0002g0117a0008c0005t0001g0115a0008c0005t0001g0118others(2): Show | 5 | HG00099.hp2 HG01070.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-7015T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098169 | ||||||
| chr9:115098180
|
G | A | 24 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(21): Show | 24 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-136-7026C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098180 | ||||||
| chr9:115098189
|
C | T | 137 | a0001c0002t0001g0192a0001c0009t0001g0101a0001c0009t0001g0123others(134): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-136-7035G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098189 | ||||||
| chr9:115098229
|
C | T | 68 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(65): Show | 69 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.-136-7075G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098229 | ||||||
| chr9:115098285
|
G | A | 1 | a0046c0053t0018g0245 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-136-7131C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098285 | ||||||
| chr9:115098672
|
G | A | 218 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(215): Show | 220 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-136-7518C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098672 | ||||||
| chr9:115098762
|
C | T | 1 | a0005c0017t0002g0078 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-136-7608G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098762 | ||||||
| chr9:115098764
|
C | A | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-136-7610G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098764 | ||||||
| chr9:115098938
|
A | ATTT | 6 | a0005c0037t0004g0152a0012c0012t0006g0062a0023c0033t0001g0126others(3): Show | 6 | HG00323.hp1 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-7787_-136-778 others(7): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | ||||||
| chr9:115098938
|
A | ATTTT | 46 | a0001c0009t0001g0244a0003c0003t0001g0229a0003c0003t0001g0239others(43): Show | 47 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.-136-7788_-136-778 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | ||||||
| chr9:115098938
|
A | ATTTTT | 103 | a0001c0002t0001g0267a0001c0002t0001g0268a0001c0002t0001g0275others(100): Show | 104 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-136-7789_-136-778 others(9): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | ||||||
| chr9:115098938
|
A | ATTTTTT | 19 | a0001c0002t0010g0288a0003c0003t0001g0279a0003c0003t0003g0053others(16): Show | 19 | HG00280.hp2 HG01175.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-136-7790_-136-778 others(10): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | ||||||
| chr9:115098938
|
A | ATTTTTTT | 20 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(17): Show | 20 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136-7791_-136-778 others(11): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | ||||||
| chr9:115098938
|
A | T | 2 | a0005c0067t0002g0359a0030c0047t0001g0358 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-136-7784T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | ||||||
| chr9:115098938
|
ATT | A | 120 | a0001c0002t0001g0192a0001c0009t0001g0101a0001c0009t0001g0123others(117): Show | 123 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-136-7786_-136-778 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | ||||||
| chr9:115098938
|
ATTT | A | 17 | a0001c0009t0002g0117a0002c0001t0002g0092a0002c0001t0006g0120others(14): Show | 17 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(14): Show |
intron_variant | MODIFIER | c.-136-7787_-136-778 others(7): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | ||||||
| chr9:115098938
|
ATTTT | A | 9 | a0001c0002t0001g0128a0001c0002t0001g0322a0001c0002t0001g0323others(6): Show | 9 | HG01123.hp2 HG02258.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-7788_-136-778 others(8): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115098938 | ||||||
| chr9:115099192
|
G | A | 221 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(218): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.-136-8038C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115099192 | ||||||
| chr9:115099261
|
G | C | 47 | a0001c0009t0001g0244a0003c0003t0001g0229a0003c0003t0001g0239others(44): Show | 48 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-136-8107C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115099261 | ||||||
| chr9:115099916
|
A | C | 5 | a0003c0077t0004g0356a0013c0021t0004g0129a0013c0021t0004g0254others(2): Show | 5 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136-8762T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115099916 | ||||||
| chr9:115099931
|
G | A | 136 | a0001c0002t0001g0192a0001c0009t0001g0101a0001c0009t0001g0123others(133): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-136-8777C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115099931 | ||||||
| chr9:115099932
|
A | T | 136 | a0001c0002t0001g0192a0001c0009t0001g0101a0001c0009t0001g0123others(133): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-136-8778T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115099932 | ||||||
| chr9:115100006
|
A | G | 1 | a0005c0067t0002g0359 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-136-8852T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100006 | ||||||
| chr9:115100058
|
C | T | 1 | a0006c0007t0022g0054 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-136-8904G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100058 | ||||||
| chr9:115100227
|
A | G | 169 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-136-9073T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100227 | ||||||
| chr9:115100646
|
G | A | 1 | a0013c0021t0004g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-136-9492C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100646 | ||||||
| chr9:115100656
|
G | A | 1 | a0002c0001t0002g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-136-9502C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100656 | ||||||
| chr9:115100658
|
C | T | 1 | a0001c0024t0001g0133 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-136-9504G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100658 | ||||||
| chr9:115100720
|
C | T | 25 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(22): Show | 25 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.-136-9566G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100720 | ||||||
| chr9:115100739
|
T | G | 6 | a0007c0006t0003g0052a0007c0006t0007g0001a0007c0006t0007g0051others(3): Show | 7 | NA18947.hp2 NA18975.hp1 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136-9585A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100739 | ||||||
| chr9:115100775
|
G | C | 7 | a0005c0103t0012g0091a0017c0022t0004g0252a0017c0022t0004g0261others(4): Show | 7 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136-9621C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100775 | ||||||
| chr9:115100808
|
A | G | 3 | a0017c0022t0004g0252a0017c0022t0004g0261a0050c0063t0012g0149 | 3 | HG02647.hp1 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-9654T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100808 | ||||||
| chr9:115100838
|
A | G | 1 | a0003c0013t0001g0285 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-136-9684T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100838 | ||||||
| chr9:115100841
|
C | T | 1 | a0002c0001t0002g0169 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-136-9687G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100841 | ||||||
| chr9:115100920
|
A | T | 2 | a0003c0003t0001g0283a0004c0004t0002g0284 | 2 | NA18968.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-136-9766T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115100920 | ||||||
| chr9:115101135
|
C | T | 24 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(21): Show | 24 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-136-9981G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101135 | ||||||
| chr9:115101175
|
G | A | 1 | a0008c0005t0001g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-136-10021C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101175 | ||||||
| chr9:115101204
|
C | G | 46 | a0002c0001t0007g0018a0007c0006t0003g0028a0007c0006t0003g0052others(43): Show | 47 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-136-10050G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101204 | ||||||
| chr9:115101275
|
G | A | 1 | a0003c0013t0001g0282 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-136-10121C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101275 | ||||||
| chr9:115101328
|
C | G | 9 | a0003c0035t0004g0150a0003c0035t0004g0151a0004c0051t0004g0342others(6): Show | 9 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-136-10174G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101328 | ||||||
| chr9:115101345
|
G | T | 3 | a0001c0002t0001g0138a0001c0002t0001g0141a0001c0002t0001g0142 | 3 | NA18956.hp2 NA18959.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-136-10191C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101345 | ||||||
| chr9:115101405
|
A | G | 84 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(81): Show | 85 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.-136-10251T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101405 | ||||||
| chr9:115101493
|
G | A | 1 | a0002c0096t0002g0156 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-136-10339C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101493 | ||||||
| chr9:115101587
|
A | T | 5 | a0007c0006t0003g0028a0010c0008t0003g0013a0010c0008t0003g0014others(2): Show | 5 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-10433T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101587 | ||||||
| chr9:115101623
|
A | T | 1 | a0002c0001t0002g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-136-10469T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101623 | ||||||
| chr9:115101631
|
A | G | 1 | a0002c0001t0002g0157 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-136-10477T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101631 | ||||||
| chr9:115101632
|
T | C | 75 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(72): Show | 76 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.-136-10478A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101632 | ||||||
| chr9:115101644
|
C | T | 3 | a0017c0022t0004g0252a0017c0022t0004g0261a0050c0063t0012g0149 | 3 | HG02647.hp1 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-10490G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101644 | ||||||
| chr9:115101675
|
A | T | 9 | a0009c0092t0002g0093a0012c0012t0006g0057a0012c0012t0006g0058others(6): Show | 9 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-10521T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101675 | ||||||
| chr9:115101676
|
A | G | 2 | a0004c0018t0004g0224a0006c0007t0005g0204 | 2 | HG02145.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-136-10522T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101676 | ||||||
| chr9:115101805
|
A | C | 355 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(352): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-136-10651T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101805 | ||||||
| chr9:115101870
|
G | T | 355 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(352): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-136-10716C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115101870 | ||||||
| chr9:115102068
|
T | C | 1 | a0002c0001t0002g0100 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-136-10914A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102068 | ||||||
| chr9:115102078
|
C | T | 1 | a0001c0002t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-136-10924G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102078 | ||||||
| chr9:115102207
|
A | G | 1 | a0003c0013t0001g0282 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-136-11053T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102207 | ||||||
| chr9:115102330
|
C | T | 216 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(213): Show | 218 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.-136-11176G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102330 | ||||||
| chr9:115102398
|
A | G | 215 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(212): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.-136-11244T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102398 | ||||||
| chr9:115102646
|
G | T | 20 | a0001c0009t0001g0244a0003c0003t0001g0229a0003c0003t0001g0239others(17): Show | 21 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-136-11492C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102646 | ||||||
| chr9:115102706
|
A | G | 2 | a0001c0009t0001g0101a0038c0088t0002g0097 | 2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-136-11552T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102706 | ||||||
| chr9:115102927
|
G | A | 7 | a0004c0051t0004g0342a0005c0034t0002g0197a0005c0034t0002g0198others(4): Show | 7 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136-11773C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102927 | ||||||
| chr9:115102996
|
C | G | 132 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(129): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-136-11842G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115102996 | ||||||
| chr9:115103097
|
G | A | 145 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(142): Show | 146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-136-11943C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103097 | ||||||
| chr9:115103200
|
T | C | 1 | a0006c0007t0005g0324 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-136-12046A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103200 | ||||||
| chr9:115103217
|
G | A | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-136-12063C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103217 | ||||||
| chr9:115103224
|
C | T | 2 | a0010c0008t0003g0027a0010c0008t0003g0032 | 2 | NA19010.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-136-12070G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103224 | ||||||
| chr9:115103227
|
T | C | 2 | a0005c0034t0002g0197a0005c0034t0002g0198 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-136-12073A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103227 | ||||||
| chr9:115103363
|
A | G | 355 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(352): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-136-12209T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103363 | ||||||
| chr9:115103383
|
T | A | 2 | a0002c0001t0002g0167a0009c0031t0001g0166 | 2 | NA19002.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-136-12229A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103383 | ||||||
| chr9:115103547
|
A | G | 169 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-136-12393T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103547 | ||||||
| chr9:115103549
|
A | G | 13 | a0003c0003t0001g0344a0003c0003t0004g0337a0005c0037t0004g0271others(10): Show | 13 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136-12395T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103549 | ||||||
| chr9:115103666
|
G | A | 7 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(4): Show | 7 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136-12512C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103666 | ||||||
| chr9:115103952
|
G | A | 1 | a0002c0001t0002g0168 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-136-12798C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103952 | ||||||
| chr9:115103957
|
A | G | 46 | a0002c0001t0007g0018a0007c0006t0003g0028a0007c0006t0003g0052others(43): Show | 47 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-136-12803T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103957 | ||||||
| chr9:115103966
|
A | G | 1 | a0002c0001t0002g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-136-12812T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103966 | ||||||
| chr9:115103967
|
GATCC | G | 38 | a0001c0009t0001g0123a0001c0009t0002g0117a0001c0009t0010g0107others(35): Show | 39 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.-136-12817_-136-12 others(10): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103967 | ||||||
| chr9:115103976
|
A | G | 1 | a0008c0005t0001g0102 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-136-12822T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115103976 | ||||||
| chr9:115104039
|
A | G | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136-12885T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104039 | ||||||
| chr9:115104145
|
A | G | 169 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-136-12991T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104145 | ||||||
| chr9:115104433
|
G | A | 1 | a0004c0004t0002g0325 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-136-13279C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104433 | ||||||
| chr9:115104467
|
A | G | 1 | a0007c0006t0017g0012 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-136-13313T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104467 | ||||||
| chr9:115104667
|
C | T | 132 | a0001c0002t0001g0192a0001c0009t0001g0123a0001c0009t0001g0155others(129): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-137+13315G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104667 | ||||||
| chr9:115104699
|
T | C | 1 | a0049c0064t0014g0343 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-137+13283A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104699 | ||||||
| chr9:115104809
|
G | C | 1 | a0002c0001t0002g0168 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-137+13173C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104809 | ||||||
| chr9:115104894
|
C | T | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-137+13088G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115104894 | ||||||
| chr9:115105113
|
A | T | 3 | a0001c0002t0001g0134a0001c0002t0013g0135a0002c0020t0002g0148 | 3 | HG02071.hp1 NA18747.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-137+12869T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105113 | ||||||
| chr9:115105228
|
C | T | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+12754G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105228 | ||||||
| chr9:115105270
|
C | G | 1 | a0003c0035t0004g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-137+12712G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105270 | ||||||
| chr9:115105298
|
G | T | 6 | a0017c0022t0004g0252a0017c0022t0004g0261a0029c0046t0004g0339others(3): Show | 6 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+12684C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105298 | ||||||
| chr9:115105679
|
G | T | 133 | a0001c0002t0001g0192a0001c0009t0001g0123a0001c0009t0001g0155others(130): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.-137+12303C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105679 | ||||||
| chr9:115105740
|
G | C | 6 | a0003c0003t0004g0337a0005c0037t0004g0271a0005c0067t0002g0359others(3): Show | 6 | HG02109.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+12242C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105740 | ||||||
| chr9:115105844
|
T | C | 1 | a0001c0009t0001g0244 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-137+12138A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105844 | ||||||
| chr9:115105948
|
G | A | 1 | a0034c0060t0014g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-137+12034C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115105948 | ||||||
| chr9:115106040
|
T | C | 215 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(212): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.-137+11942A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106040 | ||||||
| chr9:115106063
|
G | C | 8 | a0003c0027t0002g0214a0003c0027t0002g0215a0003c0027t0002g0218others(5): Show | 8 | HG02895.hp1 HG02897.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+11919C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106063 | ||||||
| chr9:115106064
|
A | G | 9 | a0003c0003t0001g0279a0003c0003t0019g0273a0003c0003t0019g0360others(6): Show | 9 | HG01081.hp1 HG01175.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.-137+11918T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106064 | ||||||
| chr9:115106130
|
T | G | 3 | a0023c0033t0001g0126a0023c0033t0001g0127a0023c0033t0001g0338 | 3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-137+11852A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106130 | ||||||
| chr9:115106419
|
A | C | 24 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(21): Show | 24 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-137+11563T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106419 | ||||||
| chr9:115106863
|
G | C | 1 | a0008c0005t0002g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-137+11119C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106863 | ||||||
| chr9:115106897
|
A | G | 24 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(21): Show | 24 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-137+11085T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106897 | ||||||
| chr9:115106954
|
G | A | 4 | a0003c0003t0001g0229a0003c0003t0001g0239a0003c0003t0001g0240others(1): Show | 4 | HG00609.hp1 NA18953.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+11028C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115106954 | ||||||
| chr9:115107077
|
AT | A | 36 | a0001c0009t0001g0244a0003c0003t0001g0229a0003c0003t0001g0239others(33): Show | 37 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.-137+10904delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107077 | ||||||
| chr9:115107138
|
T | G | 68 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(65): Show | 69 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.-137+10844A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107138 | ||||||
| chr9:115107278
|
T | C | 4 | a0013c0021t0004g0129a0013c0021t0004g0254a0013c0021t0004g0255others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+10704A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107278 | ||||||
| chr9:115107392
|
A | G | 15 | a0001c0002t0001g0192a0001c0009t0010g0163a0001c0011t0001g0161others(12): Show | 15 | HG02040.hp2 HG02080.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-137+10590T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107392 | ||||||
| chr9:115107405
|
T | G | 169 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-137+10577A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107405 | ||||||
| chr9:115107591
|
C | T | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+10391G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107591 | ||||||
| chr9:115107651
|
C | T | 132 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(129): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-137+10331G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107651 | ||||||
| chr9:115107804
|
A | G | 2 | a0026c0036t0002g0202a0026c0036t0002g0203 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-137+10178T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107804 | ||||||
| chr9:115107861
|
A | T | 1 | a0004c0051t0004g0342 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-137+10121T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107861 | ||||||
| chr9:115107951
|
C | T | 132 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(129): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-137+10031G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107951 | ||||||
| chr9:115107964
|
G | A | 1 | a0001c0009t0001g0188 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-137+10018C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115107964 | ||||||
| chr9:115108079
|
A | G | 3 | a0023c0033t0001g0126a0023c0033t0001g0127a0023c0033t0001g0338 | 3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-137+9903T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108079 | ||||||
| chr9:115108240
|
C | T | 2 | a0005c0034t0002g0197a0005c0034t0002g0198 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-137+9742G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108240 | ||||||
| chr9:115108494
|
G | T | 8 | a0009c0092t0002g0093a0012c0012t0006g0057a0012c0012t0006g0058others(5): Show | 8 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+9488C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108494 | ||||||
| chr9:115108500
|
T | G | 2 | a0013c0021t0004g0129a0013c0021t0004g0256 | 2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-137+9482A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108500 | ||||||
| chr9:115108549
|
T | A | 1 | a0001c0009t0001g0123 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-137+9433A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108549 | ||||||
| chr9:115108561
|
C | T | 1 | a0004c0004t0002g0278 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-137+9421G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108561 | ||||||
| chr9:115108656
|
G | T | 5 | a0001c0002t0001g0267a0001c0002t0001g0268a0001c0002t0001g0275others(2): Show | 5 | HG01069.hp1 HG01074.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+9326C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108656 | ||||||
| chr9:115108705
|
C | A | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+9277G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115108705 | ||||||
| chr9:115109149
|
A | G | 1 | a0002c0001t0002g0100 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-137+8833T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115109149 | ||||||
| chr9:115109458
|
A | G | 1 | a0001c0002t0001g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-137+8524T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115109458 | ||||||
| chr9:115109790
|
C | T | 1 | a0004c0004t0002g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-137+8192G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115109790 | ||||||
| chr9:115109799
|
T | G | 7 | a0005c0103t0012g0091a0017c0022t0004g0252a0017c0022t0004g0261others(4): Show | 7 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+8183A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115109799 | ||||||
| chr9:115109897
|
A | T | 2 | a0001c0009t0001g0155a0001c0009t0001g0160 | 2 | NA18939.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-137+8085T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115109897 | ||||||
| chr9:115109978
|
T | A | 24 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(21): Show | 24 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-137+8004A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115109978 | ||||||
| chr9:115110004
|
T | C | 16 | a0003c0077t0004g0356a0013c0021t0004g0129a0013c0021t0004g0254others(13): Show | 16 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-137+7978A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110004 | ||||||
| chr9:115110110
|
C | A | 2 | a0010c0008t0003g0027a0010c0008t0003g0032 | 2 | NA19010.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-137+7872G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110110 | ||||||
| chr9:115110123
|
G | A | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+7859C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110123 | ||||||
| chr9:115110284
|
C | T | 4 | a0004c0045t0002g0230a0004c0045t0002g0231a0006c0015t0002g0241others(1): Show | 4 | HG00741.hp1 HG01358.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+7698G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110284 | ||||||
| chr9:115110417
|
GGTTGCTG others(18): Show |
G | 7 | a0005c0103t0012g0091a0017c0022t0004g0252a0017c0022t0004g0261others(4): Show | 7 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+7540_-137+756 others(29): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110417 | ||||||
| chr9:115110421
|
G | T | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+7561C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110421 | ||||||
| chr9:115110500
|
G | A | 1 | a0018c0028t0012g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-137+7482C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110500 | ||||||
| chr9:115110564
|
A | G | 19 | a0001c0009t0001g0244a0003c0003t0001g0229a0003c0003t0001g0239others(16): Show | 20 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.-137+7418T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110564 | ||||||
| chr9:115110737
|
G | A | 1 | a0001c0002t0008g0144 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-137+7245C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110737 | ||||||
| chr9:115110754
|
G | C | 1 | a0004c0050t0014g0345 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-137+7228C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110754 | ||||||
| chr9:115110878
|
A | AT | 8 | a0005c0034t0002g0197a0005c0034t0002g0198a0009c0044t0001g0335others(5): Show | 8 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+7103dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110878 | ||||||
| chr9:115110878
|
AT | A | 280 | a0001c0002t0001g0128a0001c0002t0001g0192a0001c0002t0001g0267others(277): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-137+7103delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110878 | ||||||
| chr9:115110878
|
ATT | A | 6 | a0001c0009t0015g0124a0001c0009t0015g0350a0002c0001t0002g0158others(3): Show | 6 | HG00738.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+7102_-137+710 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110878 | ||||||
| chr9:115110948
|
C | T | 1 | a0002c0001t0002g0098 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+7034G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110948 | ||||||
| chr9:115110958
|
C | T | 1 | a0003c0013t0001g0272 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-137+7024G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110958 | ||||||
| chr9:115110966
|
G | A | 6 | a0007c0006t0003g0052a0007c0006t0007g0001a0007c0006t0007g0051others(3): Show | 7 | NA18947.hp2 NA18975.hp1 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.-137+7016C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115110966 | ||||||
| chr9:115111046
|
A | T | 1 | a0011c0010t0001g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+6936T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111046 | ||||||
| chr9:115111071
|
G | A | 1 | a0001c0002t0001g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-137+6911C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111071 | ||||||
| chr9:115111072
|
G | A | 138 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-137+6910C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111072 | ||||||
| chr9:115111104
|
T | C | 3 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257 | 3 | HG02559.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-137+6878A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111104 | ||||||
| chr9:115111160
|
C | T | 2 | a0003c0035t0004g0150a0003c0035t0004g0151 | 2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-137+6822G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111160 | ||||||
| chr9:115111215
|
G | A | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+6767C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111215 | ||||||
| chr9:115111221
|
T | C | 1 | a0005c0061t0002g0257 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-137+6761A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111221 | ||||||
| chr9:115111249
|
G | A | 7 | a0004c0051t0004g0342a0005c0034t0002g0197a0005c0034t0002g0198others(4): Show | 7 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+6733C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111249 | ||||||
| chr9:115111385
|
T | TTC | 14 | a0001c0009t0001g0244a0003c0003t0001g0239a0003c0003t0001g0240others(11): Show | 15 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-137+6595_-137+659 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111385 | ||||||
| chr9:115111399
|
C | CT | 115 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0275others(112): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-137+6582dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
C | CTCTCTTT others(8): Show |
1 | a0002c0098t0002g0147 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-137+6582_-137+658 others(19): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
C | CTCTCTTT others(10): Show |
2 | a0002c0020t0001g0145a0009c0099t0001g0146 | 2 | HG02071.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.-137+6582_-137+658 others(21): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
C | CTCTCTTT others(11): Show |
5 | a0001c0002t0003g0007a0001c0002t0013g0135a0001c0024t0003g0008others(2): Show | 5 | NA18747.hp2 NA18992.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+6582_-137+658 others(22): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
C | CTCTCTTT others(12): Show |
5 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(2): Show | 5 | HG02071.hp1 HG02698.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+6582_-137+658 others(23): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
C | CTCTCTTT others(13): Show |
4 | a0001c0002t0001g0138a0001c0002t0008g0139a0009c0044t0001g0140others(1): Show | 4 | HG02080.hp2 NA18948.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+6582_-137+658 others(24): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
C | CTCTCTTT others(14): Show |
2 | a0001c0002t0008g0136a0001c0002t0008g0137 | 2 | NA18999.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-137+6582_-137+658 others(25): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
C | CTCTTTTT others(8): Show |
4 | a0005c0061t0002g0257a0013c0021t0004g0254a0013c0021t0004g0255others(1): Show | 4 | HG02572.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+6582_-137+658 others(19): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
C | CTCTTTTT others(9): Show |
1 | a0013c0021t0004g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-137+6582_-137+658 others(20): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
C | CTCTTTTT others(14): Show |
1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-137+6582_-137+658 others(25): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
C | CTT | 10 | a0001c0002t0001g0268a0003c0003t0001g0199a0004c0004t0001g0269others(7): Show | 10 | HG01433.hp2 HG01952.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-137+6581_-137+658 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
C | CTTTTTTT others(4): Show |
2 | a0022c0025t0001g0348a0022c0025t0001g0349 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-137+6572_-137+658 others(15): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
C | CTTTTTTT others(5): Show |
1 | a0022c0025t0001g0347 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-137+6571_-137+658 others(16): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
C | CTTTTTTT others(8): Show |
1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-137+6568_-137+658 others(19): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
CT | C | 42 | a0002c0001t0002g0195a0002c0001t0007g0018a0003c0003t0001g0332others(39): Show | 43 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.-137+6582delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
CTT | C | 84 | a0001c0009t0001g0101a0001c0009t0001g0123a0001c0009t0001g0155others(81): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-137+6581_-137+658 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
CTTT | C | 14 | a0001c0002t0001g0192a0001c0024t0001g0133a0002c0001t0002g0125others(11): Show | 14 | HG01099.hp2 HG02040.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-137+6580_-137+658 others(7): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
CTTTTTTT | C | 6 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(3): Show | 6 | HG01346.hp2 HG03017.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+6576_-137+658 others(11): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
CTTTTTTT others(1): Show |
C | 7 | a0004c0051t0004g0342a0005c0034t0002g0197a0005c0034t0002g0198others(4): Show | 7 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+6575_-137+658 others(12): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
CTTTTTTT others(3): Show |
C | 1 | a0005c0103t0012g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-137+6573_-137+658 others(14): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111399
|
CTTTTTTT others(7): Show |
C | 1 | a0034c0060t0014g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-137+6569_-137+658 others(18): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111399 | ||||||
| chr9:115111400
|
T | TC | 5 | a0004c0050t0014g0345a0006c0015t0002g0241a0024c0083t0001g0056others(2): Show | 5 | HG01109.hp1 HG02922.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+6581_-137+658 others(5): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111400 | ||||||
| chr9:115111402
|
T | C | 1 | a0049c0064t0014g0343 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-137+6580A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111402 | ||||||
| chr9:115111403
|
T | C | 2 | a0003c0035t0004g0150a0003c0035t0004g0151 | 2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-137+6579A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111403 | ||||||
| chr9:115111404
|
T | C | 5 | a0001c0024t0001g0133a0002c0020t0002g0065a0002c0020t0002g0249others(2): Show | 5 | HG02257.hp1 NA18995.hp1 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+6578A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111404 | ||||||
| chr9:115111405
|
T | C | 3 | a0003c0035t0004g0150a0003c0035t0004g0151a0046c0053t0018g0245 | 3 | HG00323.hp1 HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-137+6577A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111405 | ||||||
| chr9:115111406
|
T | C | 4 | a0001c0024t0001g0133a0002c0020t0002g0065a0002c0020t0002g0249others(1): Show | 4 | NA18995.hp1 NA19068.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+6576A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111406 | ||||||
| chr9:115111429
|
A | T | 32 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(29): Show | 32 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.-137+6553T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111429 | ||||||
| chr9:115111431
|
G | A | 46 | a0001c0009t0001g0244a0003c0003t0001g0229a0003c0003t0001g0239others(43): Show | 47 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.-137+6551C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111431 | ||||||
| chr9:115111434
|
A | C | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+6548T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111434 | ||||||
| chr9:115111495
|
G | A | 32 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(29): Show | 32 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.-137+6487C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111495 | ||||||
| chr9:115111570
|
G | C | 1 | a0003c0003t0001g0344 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-137+6412C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111570 | ||||||
| chr9:115111599
|
C | T | 1 | a0001c0002t0001g0267 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-137+6383G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111599 | ||||||
| chr9:115111628
|
C | T | 2 | a0029c0046t0004g0339a0029c0046t0004g0340 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-137+6354G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111628 | ||||||
| chr9:115111688
|
A | G | 89 | a0001c0002t0001g0192a0001c0009t0001g0101a0001c0009t0001g0123others(86): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-137+6294T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111688 | ||||||
| chr9:115111821
|
T | A | 1 | a0002c0001t0002g0195 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-137+6161A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111821 | ||||||
| chr9:115111938
|
A | C | 1 | a0015c0029t0003g0010 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-137+6044T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111938 | ||||||
| chr9:115111976
|
T | A | 1 | a0008c0005t0001g0196 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-137+6006A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115111976 | ||||||
| chr9:115112094
|
G | C | 3 | a0027c0071t0001g0355a0028c0038t0005g0353a0028c0038t0005g0354 | 3 | HG02572.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-137+5888C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112094 | ||||||
| chr9:115112154
|
T | A | 28 | a0001c0009t0001g0244a0003c0003t0001g0229a0003c0003t0001g0239others(25): Show | 29 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.-137+5828A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112154 | ||||||
| chr9:115112245
|
C | T | 1 | a0005c0062t0026g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-137+5737G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112245 | ||||||
| chr9:115112261
|
G | C | 1 | a0034c0060t0014g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-137+5721C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112261 | ||||||
| chr9:115112326
|
C | A | 4 | a0004c0004t0002g0220a0004c0004t0002g0223a0006c0007t0005g0221others(1): Show | 4 | NA18944.hp1 NA18954.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+5656G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112326 | ||||||
| chr9:115112338
|
A | G | 1 | a0003c0003t0004g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-137+5644T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112338 | ||||||
| chr9:115112369
|
A | G | 1 | a0009c0092t0002g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-137+5613T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112369 | ||||||
| chr9:115112433
|
A | G | 3 | a0023c0033t0001g0126a0023c0033t0001g0127a0023c0033t0001g0338 | 3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-137+5549T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112433 | ||||||
| chr9:115112498
|
T | A | 19 | a0001c0009t0001g0244a0003c0003t0001g0229a0003c0003t0001g0239others(16): Show | 20 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.-137+5484A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112498 | ||||||
| chr9:115112541
|
G | A | 2 | a0003c0035t0004g0150a0003c0035t0004g0151 | 2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-137+5441C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112541 | ||||||
| chr9:115112550
|
A | G | 1 | a0004c0075t0004g0266 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-137+5432T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112550 | ||||||
| chr9:115112555
|
C | T | 1 | a0002c0096t0002g0156 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-137+5427G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112555 | ||||||
| chr9:115112634
|
C | T | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+5348G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112634 | ||||||
| chr9:115112722
|
TG | T | 4 | a0001c0011t0001g0095a0002c0001t0002g0002a0002c0001t0002g0094others(1): Show | 5 | NA19065.hp1 NA19066.hp2 NA19067.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+5259delC | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112722 | ||||||
| chr9:115112729
|
G | A | 1 | a0010c0008t0003g0034 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-137+5253C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112729 | ||||||
| chr9:115112766
|
C | A | 1 | a0005c0034t0002g0198 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-137+5216G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112766 | ||||||
| chr9:115112851
|
T | C | 205 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(202): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-137+5131A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112851 | ||||||
| chr9:115112879
|
C | T | 1 | a0001c0009t0001g0155 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-137+5103G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112879 | ||||||
| chr9:115112989
|
T | A | 1 | a0002c0001t0002g0125 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-137+4993A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112989 | ||||||
| chr9:115112997
|
G | A | 2 | a0001c0009t0001g0244a0046c0053t0018g0245 | 2 | HG00323.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-137+4985C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115112997 | ||||||
| chr9:115113120
|
G | A | 4 | a0004c0051t0004g0342a0023c0033t0001g0126a0023c0033t0001g0127others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+4862C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113120 | ||||||
| chr9:115113166
|
GC | G | 130 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(127): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.-137+4815delG | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113166 | ||||||
| chr9:115113168
|
T | A | 130 | a0001c0002t0001g0128a0001c0002t0001g0267a0001c0002t0001g0268others(127): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.-137+4814A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113168 | ||||||
| chr9:115113402
|
T | C | 135 | a0001c0002t0001g0192a0001c0009t0001g0101a0001c0009t0001g0123others(132): Show | 138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-137+4580A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113402 | ||||||
| chr9:115113409
|
A | C | 135 | a0001c0002t0001g0192a0001c0009t0001g0101a0001c0009t0001g0123others(132): Show | 138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-137+4573T>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113409 | ||||||
| chr9:115113468
|
C | T | 36 | a0001c0009t0001g0244a0003c0003t0001g0229a0003c0003t0001g0239others(33): Show | 37 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.-137+4514G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113468 | ||||||
| chr9:115113498
|
C | G | 9 | a0013c0059t0002g0067a0014c0016t0006g0069a0014c0016t0006g0071others(6): Show | 9 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.-137+4484G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113498 | ||||||
| chr9:115113622
|
T | C | 1 | a0004c0018t0004g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-137+4360A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113622 | ||||||
| chr9:115113713
|
A | T | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+4269T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113713 | ||||||
| chr9:115113726
|
G | A | 2 | a0005c0034t0002g0197a0005c0034t0002g0198 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-137+4256C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113726 | ||||||
| chr9:115113801
|
G | A | 18 | a0004c0051t0004g0342a0005c0034t0002g0197a0005c0034t0002g0198others(15): Show | 18 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-137+4181C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113801 | ||||||
| chr9:115113999
|
C | T | 3 | a0023c0033t0001g0126a0023c0033t0001g0127a0023c0033t0001g0338 | 3 | HG01884.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-137+3983G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115113999 | ||||||
| chr9:115114161
|
C | G | 1 | a0002c0001t0002g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-137+3821G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114161 | ||||||
| chr9:115114171
|
A | G | 7 | a0003c0003t0001g0344a0011c0010t0001g0064a0011c0010t0001g0227others(4): Show | 7 | HG02258.hp1 HG02615.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-137+3811T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114171 | ||||||
| chr9:115114341
|
T | C | 1 | a0011c0010t0001g0225 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-137+3641A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114341 | ||||||
| chr9:115114356
|
C | T | 45 | a0002c0001t0007g0018a0007c0006t0003g0028a0007c0006t0003g0052others(42): Show | 46 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.-137+3626G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114356 | ||||||
| chr9:115114365
|
C | T | 1 | a0002c0001t0002g0092 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-137+3617G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114365 | ||||||
| chr9:115114411
|
G | A | 1 | a0053c0104t0028g0341 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-137+3571C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114411 | ||||||
| chr9:115114549
|
G | A | 1 | a0007c0006t0007g0035 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-137+3433C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114549 | ||||||
| chr9:115114694
|
A | G | 1 | a0001c0011t0008g0153 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-137+3288T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114694 | ||||||
| chr9:115114784
|
T | C | 9 | a0013c0059t0002g0067a0014c0016t0006g0069a0014c0016t0006g0071others(6): Show | 9 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.-137+3198A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114784 | ||||||
| chr9:115114836
|
T | C | 2 | a0004c0004t0002g0333a0004c0018t0004g0334 | 2 | HG02698.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-137+3146A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114836 | ||||||
| chr9:115114923
|
A | ACACATAG others(4): Show |
355 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(352): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-137+3058_-137+305 others(15): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114923 | ||||||
| chr9:115114933
|
CT | C | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+3048delA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114933 | ||||||
| chr9:115114965
|
G | A | 1 | a0004c0018t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-137+3017C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114965 | ||||||
| chr9:115114971
|
T | G | 13 | a0003c0035t0004g0150a0003c0035t0004g0151a0003c0077t0004g0356others(10): Show | 13 | HG01192.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-137+3011A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115114971 | ||||||
| chr9:115115046
|
G | T | 1 | a0003c0077t0004g0356 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-137+2936C>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115046 | ||||||
| chr9:115115047
|
C | T | 2 | a0017c0022t0004g0130a0017c0022t0004g0131 | 2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-137+2935G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115047 | ||||||
| chr9:115115048
|
G | A | 1 | a0052c0057t0014g0346 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-137+2934C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115048 | ||||||
| chr9:115115101
|
A | G | 7 | a0005c0103t0012g0091a0017c0022t0004g0252a0017c0022t0004g0261others(4): Show | 7 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+2881T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115101 | ||||||
| chr9:115115108
|
TAG | T | 22 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(19): Show | 22 | HG02071.hp1 HG02080.hp2 HG02698.hp2 others(19): Show |
intron_variant | MODIFIER | c.-137+2872_-137+287 others(6): Show |
TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115108 | ||||||
| chr9:115115207
|
C | T | 8 | a0008c0005t0001g0083a0008c0005t0001g0084a0008c0005t0001g0085others(5): Show | 8 | HG00140.hp2 HG00738.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+2775G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115207 | ||||||
| chr9:115115232
|
T | A | 19 | a0007c0006t0003g0052a0007c0006t0007g0001a0007c0006t0007g0006others(16): Show | 20 | HG00408.hp1 HG00558.hp2 NA18947.hp2 others(17): Show |
intron_variant | MODIFIER | c.-137+2750A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115232 | ||||||
| chr9:115115478
|
T | C | 8 | a0003c0035t0004g0150a0003c0035t0004g0151a0005c0061t0002g0257others(5): Show | 8 | HG01192.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+2504A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115478 | ||||||
| chr9:115115862
|
C | T | 53 | a0003c0003t0001g0199a0003c0003t0001g0207a0003c0003t0001g0208others(50): Show | 53 | HG01346.hp2 HG01884.hp1 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.-137+2120G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115862 | ||||||
| chr9:115115887
|
G | A | 2 | a0017c0022t0004g0130a0017c0022t0004g0131 | 2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-137+2095C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115887 | ||||||
| chr9:115115909
|
T | C | 21 | a0001c0002t0001g0134a0001c0002t0001g0138a0001c0002t0001g0141others(18): Show | 21 | HG02071.hp1 HG02071.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.-137+2073A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115115909 | ||||||
| chr9:115116055
|
T | A | 216 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(213): Show | 218 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.-137+1927A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116055 | ||||||
| chr9:115116191
|
T | G | 209 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(206): Show | 211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.-137+1791A>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116191 | ||||||
| chr9:115116232
|
G | C | 1 | a0003c0003t0001g0336 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-137+1750C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116232 | ||||||
| chr9:115116422
|
G | A | 1 | a0003c0003t0004g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-137+1560C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116422 | ||||||
| chr9:115116632
|
G | A | 97 | a0001c0002t0001g0128a0001c0009t0001g0101a0001c0009t0001g0123others(94): Show | 98 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.-137+1350C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116632 | ||||||
| chr9:115116860
|
A | G | 13 | a0003c0003t0001g0344a0004c0050t0014g0345a0004c0051t0004g0342others(10): Show | 13 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-137+1122T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116860 | ||||||
| chr9:115116879
|
G | A | 3 | a0001c0002t0001g0134a0001c0002t0013g0135a0002c0020t0002g0148 | 3 | HG02071.hp1 NA18747.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-137+1103C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116879 | ||||||
| chr9:115116933
|
C | A | 275 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(272): Show | 279 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.-137+1049G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115116933 | ||||||
| chr9:115117061
|
C | T | 6 | a0005c0067t0002g0359a0017c0022t0004g0261a0018c0028t0012g0258others(3): Show | 6 | HG01496.hp1 HG02280.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+921G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117061 | ||||||
| chr9:115117135
|
A | G | 179 | a0001c0002t0001g0134a0001c0002t0001g0192a0001c0002t0003g0007others(176): Show | 182 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-137+847T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117135 | ||||||
| chr9:115117174
|
C | G | 8 | a0005c0017t0001g0081a0005c0017t0002g0076a0005c0017t0002g0078others(5): Show | 8 | HG01346.hp2 HG02922.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+808G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117174 | ||||||
| chr9:115117231
|
C | T | 1 | a0005c0017t0002g0076 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-137+751G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117231 | ||||||
| chr9:115117285
|
G | C | 1 | a0002c0020t0002g0148 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-137+697C>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117285 | ||||||
| chr9:115117340
|
C | T | 3 | a0003c0035t0004g0150a0003c0035t0004g0151a0050c0063t0012g0149 | 3 | HG02559.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-137+642G>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117340 | ||||||
| chr9:115117418
|
G | A | 2 | a0017c0022t0004g0130a0017c0022t0004g0131 | 2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-137+564C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117418 | ||||||
| chr9:115117489
|
T | C | 3 | a0005c0067t0002g0359a0006c0007t0005g0357a0030c0047t0001g0358 | 3 | HG02280.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-137+493A>G | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117489 | ||||||
| chr9:115117574
|
C | G | 1 | a0007c0006t0007g0006 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-137+408G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117574 | ||||||
| chr9:115117689
|
G | A | 65 | a0001c0002t0001g0128a0001c0009t0001g0101a0001c0009t0001g0123others(62): Show | 66 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.-137+293C>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117689 | ||||||
| chr9:115117699
|
A | T | 1 | a0003c0003t0019g0360 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-137+283T>A | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117699 | ||||||
| chr9:115117848
|
C | CT | 76 | a0001c0002t0001g0128a0001c0009t0001g0101a0001c0009t0001g0123others(73): Show | 77 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.-137+133dupA | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117848 | ||||||
| chr9:115117852
|
T | A | 1 | a0003c0003t0019g0360 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-137+130A>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117852 | ||||||
| chr9:115117861
|
C | A | 1 | a0005c0023t0018g0361 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-137+121G>T | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117861 | ||||||
| chr9:115117870
|
A | G | 93 | a0001c0002t0001g0128a0001c0002t0001g0134a0001c0002t0001g0138others(90): Show | 94 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.-137+112T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117870 | ||||||
| chr9:115117878
|
C | G | 8 | a0011c0010t0001g0064a0012c0012t0006g0057a0012c0012t0006g0058others(5): Show | 8 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+104G>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117878 | ||||||
| chr9:115117942
|
A | G | 2 | a0024c0082t0004g0055a0024c0083t0001g0056 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-137+40T>C | TNC | ENSG00000041982.17 | transcript | ENST00000350763.9 | protein_coding | 1/27 | chr9 | 115117942 |